Friday, December 13, 2013

WITH PRESENT KNOWLEDGE , CAN WE SUCCEED IN CONTROLLING SCHISTOSOMIASIS IN INDIA

This is the second lecture delivered in the winter course at IVRI,Izatnagar on 11th Dec 2013 and i am reproducing the same here . I will appreciate to receive any comments which may further the subject .It will be my pleasure if any research organisation is interested to collaborate in this endeavor. 

                                                                M C AGRAWAL
                              FORMER NATIONATIONAL FELLOW AND EMERITUS SCIENTIST
                                 COLLEGE OF VETERINARY SCIENCE AND A H , JABALPUR 482001
                                                             drmcagrawal@gmail.com    


It is heartening to note that one part of this winter course is to teach molecular techniques about control of parasitic diseases .In the past also, there had been some advance courses and discussion about control of parasitic diseases . But whether these discussions and advance courses can lead to  control of parasitic diseases ? Obviously, the answer is no. Now, with the changing time, it becomes imperative to know why we need to control parasitic diseases, which diseases are given priorities , and how we can control  these parasitic diseases.  And this is what I am going to discuss ; thus my lecture will not be a mere academic exercise of citing references  from some research papers. There is now time ,we should discuss how we may try to control parasitic diseases and what should be our research priorities that may help in achieving these goals.   
                If we analyze disease control program of our country, it will be clear that the country has given top priority ,logically ,for controlling those infectious diseases that are affecting human population. Thus there are central government’s programs for controlling tuberculosis, malaria, filariasis, guinea worm or naru  ,polio (small pox already eradicated ) etc Interestingly, almost no attention is paid on zoonotic aspects of these diseases  or medical faculty has  not taken diseases where animals are playing a crucial role in their maintenance. For example, we have not taken sincere  steps for controlling rabies .This reflects how wide apart are the two professions (medical and veterinary) which are supplementary to each other  to combat zoonotic infections of the country.
                When we come to animal diseases ,the control programs have been launched only to limited diseases like Rinder-pest, FMD, anthrax with vaccination programs of these and other infectious animal diseases. These are also the diseases ,where the veterinary hospitals ,districts and states generate the data and pass on to government of India.
                Has government of India ever launched any control program related to any parasitic disease of our domestic animal ? Here I mean control program like that of Rinder-pest or FMD . To my knowledge, there was or is  none. No doubt there have been some vaccination programs for controlling parasitic diseases . The one was about lung-worm vaccination for controlling lung-worm infection of sheep and goats ,particularly in Jammu & Kashmir , Himachal Pradesh ( now, vaccine production has been stopped by IVRI though infection is still existing ).  The other is Theileria vaccine produced by NDDB and supplied for controlling theileriosis among cross bred cattle . Again , this is not a infection which is affecting all our domestic animals. Thus we have attempted to control a infection (lung-worm) which is restricted to certain states or a infection which is affecting limited number of our domestic animals. And we have shied  away in paying our attention to the parasitic diseases which are affecting almost all domestic animals and existing in  all the states. Therefore, we have come to a crucial point where we need answer of above questions - why we need to control parasitic diseases, which diseases are given priorities , and how we can control  these parasitic diseases.  And my this short lecture will try to discuss some of these points with the hope that you , our young Parasitologists ,will devote some time to find answers of these and related  questions which are important for controlling parasitic diseases in the country. Answer of these questions are important as you will agree with me that all your research efforts will not fructify unless and until you attempt to control the parasitic infections in our country, thereby reduce mortality and animal production losses.
WHERE IS THE DATA :
If you go to any funding agency or even any government, the obvious question will be why we wish to control the particular parasitic disease. Naturally, you will put up the data about mortality and pathology of that parasitic disease . By the way, from where have you collected these data ? From some research paper or a review article or from a book ?  And how they have calculated these data  ?
I am sure that your data have not been collected from veterinary hospitals of the state or Animal Husbandry department of the country . And when these data have not been collected from the villages whether they are representing correct scenario of the infection is debatable.
VETERINARY RECORDS :
What I have said above, is all because of my experiences . While working on my book “Schistosomes and schistosomiasis in South Asia” (Agrawal,2012) ,I tried to collect the data of nasal and hepatic schistosomiasis from veterinary hospitals and veterinary diagnostic laboratories (division level),state and central governments ;  as ,in my opinion, compilation of data from these sources is important since research journals fail to provide a detailed view of the infection ; these journals have not reported each and every outbreak or prevalence of the infection in each animal species from each geographical area .
                To my dismay, I could not collect any data, related to schistosomiasis, from any of above  source ,details have been discussed in my book .Here, it will be suffice to mention :
·         There is no direction from the government to keep record of parasitic diseases and details thereof. Neither any data are passed to state or central government .
·         The veterinary hospital registers are maintained in such a way that you cannot extract any information from them. Even it is difficult to differentiate between new and repeat cases, cattle and poultry  (I have written about this topic which has been published in the news letter of National Academy of Veterinary Sciences when Dr S K Ranjan was the President).
·         The veterinary diagnostic laboratories are vague in their reporting and counter checking is missing . While reporting coprological results (generally by direct wet smear method ) ,generally positive cases are reported  as “positive for helminth or fluke or roundworm eggs” . Thus they have not differentiated the eggs where it was easy to differentiate .
It is clear that we need changes in above system and a fresh outlook  is needed to the problem so that  we will be able to  collect the data related to parasitic diseases.
WHICH PARASITIC DISEASES TO CONTROL ON PRIORITY :
This is an important question  that if we decide to control parasitic diseases what should be our priorities ?
Answer of this  question , at first hand, appears simple i.e.  the parasitic disease which is causing greatest mortality and highest pathogenecity in domestic animals should be  attended first. But how we will reach to this conclusion when we have not generated data in this regards. And when we are attempting to generate the data, are we using sensitive and specific methodologies  ? This aspect is important else our results will not be accurate. While deciding importance of the disease, we have to examine its prevalence in each animal species, age and sex wise ; the seasons when disease is occurring; animal husbandry practices  and  geographical areas where infection is existing.
With the above, two more important aspects are also linked . One is the mortality occurring in the infected animals. It may happen, looking to Indian conditions, that the animal is not infected with single parasitic infection but multiple infections and in such cases we have to device methods for ascribing death etiology . The other aspect is related to pathology of the infection which is reflected to animal production losses. No doubt we will need new methodologies to decide the above facts and these may change as per advancement of our knowledge and environment. If we will not follow new techniques , there are all chances of making mistakes as has been done while reporting schistosomiasis in post-mortem cases ( Rathore,1998).
PRIORITY AMONG HELMINTHIC DISEASE :
As my present discussion is related to schistosomiasis, I may raise a question to you – which is the most important helminthic disease of our domestic animals ? Some of you will answer - haemonchosis, or gastro-intestinal nematodiasis, others may answer fasciolosis , or amphistomosis ; while some of you will say nasal schistosomiasis but  a few or none will ascribe hepatic schistosomiasis as the most important helminthic problem of our domestic animals . May I ask the reasons for your such conclusion ?
Those who are ascribing fasciolosis as most important helminthic disease will put forward their slaughter house experience where most of the livers yield adult Fasciola gigantica  .Further, the faecal examination shows presence of Fasciola eggs in many cases ( its different that we are not differentiating eggs of Fasciola from those of amphistomes ). And those who are new to Indian  parasitology will cite the reference of a foreign veterinary book where fasciolosis is considered as most important helminthic disease of domestic animals.
Those who are ascribing amphistomosis as most important will support their argument that every rumen in slaughter house possess one or other species of amphistomes and almost all faecal samples are positive for amphistome eggs.
Against these arguments ,we do not have such visibility of hepatic schistosomiasis hence can not be considered as most important helminthic disease in India. I have discussed this topic elsewhere ( Agrawal,1999 2003) but will like to draw your attention to the need of employing correct techniques for reaching a correct decision. As time does not permit me to go into details of such discussion, I will mention only silent points emphasizing how important it is to use a correct technique and unbiased attitude for reaching to a correct conclusion.  I am mentioning some facts for your consideration and further investigations :
·         Fasciola gigantica, the only existing Fasciola  species in India , spreads through Lymnaea auricularia or Lymnaea acuminata which is a strict fresh water aquatic snail (unlike to amphibian  Lymnaea truncatula –intermediate host for F.hepatica) and survives only in perennial water sources hence animals will get infection only from perennial water sources.
·         F.hepatica  is more damaging to domestic animals than F.gigantica .
·         Against one species of Fasciola, there are at-least five schistosome species (Schistosoma indicum,S.spindale,S.incognitum, Orientobilharzia dattai and S.nasale) which are affecting our domestic animal species.
·         Schistosome infections spread through Indoplanorbis exustus and Lymnaea luteola – both species are capable to survive not only in perennial water sources but also in temporary water bodies thereby giving higher geographical spread.
·         A large number of amphistome species (40-42) are existing in the country (Dutt,1980) some of which have been synonymized. However, only four genera have been incriminated in pathogenesis to domestic animals .
·         In amphistomosis , it is only young animals which suffer and that too only from immature amphistomosis.
·         Many fresh water snails are acting as intermediate hosts for amphistomes hence their geographical spread is as large as that of schistosomes.
Now you have  to determine ,using new methodologies, which helminthic disease is more important in our domestic animals. Here, you might have noted one more fact  ; this importance will vary as per our husbandry practices. All these fluke infections are important only in grazing animals with limited effect in stall fed. Thus our priorities will vary as per animal species, husbandry practices and geographical areas. Therefore, you will identify  those parasitic diseases to be given national importance and those with regional importance etc. 
HOW TO CONTROL SCHISTOSOMIASIS :
We have come to the last part of our lecture .And that is if we decide to control any parasitic disease in our domestic animal , how we can control  it . I will take references from schistosomiasis which have been discussed in more details in my book (Agrawal,2012). Indeed, this is the only helminthic disease that has been given so much importance and where so many countries agreed to launch control program in collaboration with WHO (1985) . Ironically , India has not participated in such program.  Interestingly, WHO have not touched zoonotic aspects of the infection while attempting control program of human schistosomiasis . The review of this  program may high light our short comings  which are important to get rid of for achieving any success in controlling any parasitic disease and also  animal schistosomiasis in India or South Asia.
MULTIPLE APPROACH :
No disease can be controlled by following a single step approach , how so ever,  effective it may be . The infection has to be tackled from all aspects so that prevalence of it may be reduced to the levels where further transmission becomes difficult .Following multiple approaches were followed in schistosomiasis :
·         Chemotherapy
·         Health education
·         Snail control through use of molluscicides
·         Environmental modifications
You will realize that such program is not possible without a large team and funds  which a department of Parasitology of an institute cannot afford .  No doubt , this control program of schistosomiasis was able to reduce prevalence rate as well as pathogenesis ,as the latter is directly proportion to the intensity of the infection; and the success was  both due to  political will and scientific team work . Here, it will be prudent to discuss scientific reasons for their success and how it will fit in our program of controlling animal schistosomiasis in India. One important difference has to be remembered that while following any control program ,we have to monitor  not one but more than one animal species.
CHEMOTHERAPY :
The most important reason of the success ,perhaps, was mass treatment of the population with a most effective schistosomicide (Praziquantel) whose single oral dose @ 40-60 mg/kg body weight was 80-95% effective in urinary and hepatic schistosomiasis . Since the weight of children varied between 20-50 kg, the dose of Praziquantel was cost effective, beside easy in administration .
When we compare this scenario with that of India,  our schistosome species  are different from those dealt by WHO hence there are all differences in schistosome bionomics . And praziquantel against any of these Indian schistosome species (S.indicum,S.incognitum, S.spindale ) has not proved as effective as reported against S.haematobium or S.mansoni . In fact, our experimental work on pig- S.incognitum model has failed to reduce schistosomes to a significant level  with presence of left over schistosome population as high as 40% ( Shames et al 2000)  A same scenario was observed when the drug was tried in other experimental models ,with schistosome reduction ranging from 50-65% (left over fluke population between 50-35% ) ,  but using other Indian schistosome species. Ironically, no available flukicide (including anthiomaline ) was found to lead to a significant reduction in schistosome population in any experimental model, tried in our laboratory or by other workers ( Agrawal ,2012).
Therefore, it is not advisable to use Praziquantel or any other flukicide in any mass treatment program which has failed to reduce schistosome population to a significant level in our animals. This is because such use will lead to the high probability of development of resistance of left over schistosome population against praziquantel .
One more hindrance in using praziquantel for mass treatment in animal schistosomiasis is with regards to its cost for treating bovines against schistosomiasis. In one field trial against nasal schistosomiasis in Balaghat district of Madhya Pradesh , 60 tablets of Prazi Plus@ , which works out approximately to 20 mg/kg body wt was effective in eliminating completely clinical symptoms of snoring disease from 14 out of 18 cattle. However, cost of one treatment comes to Rs 1500/ per animal as market cost of two tablets is Rs 50/ (Agrawal, 2012) .
DIAGNOSTIC METHOD :
While implementing any control program, it is important to monitor the rate of infection and its  intensity in the given population prior and after the treatment. This monitoring is possible  by using a simple, rapid, economic but sensitive parasitological  diagnostic technique that may detect, light ,moderate and heavy infections. In WHO case , Kato-Katz technique was applied that fulfilled all the above criteria and was able even to detect light infections ( 24-96 epg) with presence of 1-4 eggs/slide, made of 41.7 mg of faeces (WHO,1985).  In contrast , a very low epg ,ranging between 2-4 in ruminants and 10-50 in pigs has been reported by almost all the Indian workers (Agrawal,2012) ; for this reason almost all egg detection methods have poor efficacy ,cannot be employed in control program, hence  warranting further work on this issue . We may also undertake further research on hatching process, as this has proved superior over egg detection methods.
 SNAIL CONTROL :
The snail control ,in WHO  program , was undertaken by using Niclosamide which has proved highly effective in killing the intermediate hosts i.e. Bulinus and Biomphalaria . Ironically , Niclosamide is not available in Indian markets and has to arrange its import from other country. We were able to procure Niclosamide and undertook  both experimental and field trials on fresh water snails , observing its high efficacy in killing Lymnaea luteola, Indoplanorbis exustus and Gyraulus but without affecting other water fauna and flora (Agrawal et al ,2005, Agrawal 2012).

However, ecological conditions of fresh water snails in India ,differ from those of other endemic countries. In India, these are the ponds, tanks and other water sources, both perennial and temporary , which are inhabited  by these fresh water snails, where as in endemic countries these were the rivers where snails are  surviving. Thus , we have more wide spread population of the snails , making our efforts more difficult while attempting snail control.

BIOLOGICAL CONTROL :
As use of chemical molluscicides may  cause environmental pollution , efforts are being made to find other alternatives for snail control . Work is being carried out to find Plant molluscicides which are more eco-friendly . Likewise, search is being made to find natural enemies of the snails that may be used as biological control agents for reducing snail population. However, it must be remembered that the biological enemy or competitor should not be introduced from outside the country/area as they may prove harmful afterwards as experienced by WHO (1985).
One natural enemy of young fresh water snails has been identified by us (Agrawal,2012) in the form of nymphets of dragonfly which co-habitat with the snails under same ecological conditions ; these nymphets are carnivorous in nature ,devouring young snails with their life span ranging from 1-3 years ( hence once introduced in the ponds, there is no need of re-introduction every year ). There is the need to develop the techniques for mass production of these nymphets which also feed on mosquito’s larvae (Agrawal 2012). Here is the importance and need of your molecular techniques which may pave the way of producing eggs and nymphets in large number , for their use in controlling snails or mosquito larvae.   
HYPER-PARASITISM  :
                As stated above,  Praziquantel  and  anthiomaline  are not able to kill a significant number of Indian schistosomes, which is not the case with S.haematobium or S.mansoni. There are also chances of development of resistance of the schistosome population  ,left over after wide use of these less effective  drugs. Therefore, there is the need to think alternatives against chemotherapy for parasitic diseases.
One promising area of research might be searching hyper-parasites of schistosomes or of  any other parasite which is causing disease in man and his animals. As you are aware these hyper-parasites are those organisms which parasitize on the parasite itself e.g. schistosomes . This hyper-parasite  may be a bacteria or a virus or even a fungus. We have to search those hyper parasites which are lethal to these parasites and should be host specific thereby eliminating our animals or human beings in causing any harm .  
NEED OF A NATIONAL INSTITUTE OF PARASITOLOGY :
With this lecture, I tried to discuss how ill equipped we are for launching a state or national level control program against any parasitic disease of our domestic animals. There is the need to re-think on our research programs and to develop methodologies which may help directly or indirectly in controlling parasitic diseases of the nation . But it will be a bad idea not to take any control measure and waiting for developing proper techniques or drugs  prior launching any control program . Notwithstanding these facts , management of animal excreta may greatly help in controlling parasitic diseases. If we start collecting all cattle dung to fill our gobar gas plants or to convert it into vermin-compose , this will not only control parasitic diseases but will also improve rural economy.
At last, I once again emphasize the need of a National Institute of Parasitology in country for paying proper attention on the parasitic diseases ,which are causing not only mortality but also production losses thereby affecting adversely national economy. I am avoiding repetition  what I have already said during  my lecture of Dr SC Parija oration gold medal award  in 2012 at Indore and  which has been published  in  Para Sight  2 Volume 2 ,issue 1 of IAAVP            and is also posted on my blog www.indianschistosomiasis.blogspot.com
SUMMARY :  
Launching of control program for any animal  disease which is causing mortality and production losses is important for any country . Ironically , the government of India  has launched control programs for viral and bacterial diseases but there is no control program ,ever launched by any government against any parasitic disease of our domestic animals. Neither , there is any system of collecting data ,related to animal parasitic diseases, from our veterinary hospitals and veterinary diagnostic laboratories . Therefore, it becomes difficult to answer- why we need to control parasitic diseases, which diseases are given priorities , and how we can control  these parasitic diseases ?
When we come to the question of how we can control animal schistosomiasis in India , we observed that our diagnostic technique is not sensitive due to low egg production of Indian schistosomes and requires further research. Likewise, the most effective Praziquantel drug is not able to kill significant number of Indian schistosomes with 35-50% left over blood-flukes . To circumvent this situation, it will be prudent to find out hyper-parasites of schistosomes and other parasites which will selectively kill these without harming their hosts. However, it will be futile to wait for developing proper techniques. Instead , animal excreta may be collected at mass scale and may be used in gobar gas plants or for preparing vermin-compose which will not only reduce prevalence of  parasitic diseases but will also improve rural economy.  The author has again emphasized opening a national institute of parasitology so that a holistic view may be developed towards parasitic diseases ,existing in the country .
REFERENCES :
Agrawal, M.C. 1999. Schistosomosis : an underestimated problem in animals in South Asia. World Animal Review 92 : 55-57.
Agrawal,M.C. 2003. Epidemiology of fluke infections . In (ed Sood ML)  Helminthology in India .Inrtenational Book Distributors, Deharadun . Page 511—542
Agrawal MC.  2012.  Schistosomes and schistosomiasis in South Asia. Springer India Pvt Ltd , New Delhi.
Agrawal MC ,Singh KP, George J and Gupta S 2005. Niclosamide trials on Indoplanorbis existus and Lymnaea luteola under different conditions. J Parasit Dis 29: 53-58

Dutt SC 1980. Paramphistomes and paramphistomiasis of domestic animals of India. Punjab Agriculture University, Ludhiana . Page 162.
Rathore BS  1998 . An epidemiological study on buffalo morbidity and mortality based on four year observations on 18630 buffaloes maintained at 28 livestock farms in India. Indian J Comp Microbiol.  19 :43-49
Shames N,Agrawal MC and Rao KNP 2000. Chemotherapeutic efficacy of praziquantel and closantel in experimental porcine schistosomiasis. Indian J Anim Sci 70 : 797-800
WHO  1985. The control of schistosomiasis. Technical report series 728. World Health Organization ,Geneva Page 113     



Tuesday, November 12, 2013

A DISCUSSION ON DIAGNOSIS OF ANIMAL SCHISTOSOMIASIS IN SOUTH ASIA

This is the lecture to be delivered in the  WINTER SCHOOL on MOLECULAR BIOLOGICAL APPROACHES FOR DIAGNOSIS AND CONTROL OF PARASITIC DISEASES at IVRI , Izatnagar in December ,2013. I am posting it on my blog for wider circulation among  scientific community, who are interested in schistosomiasis: will be pleased to see their comments. 


  
                                                                        M C AGRAWAL
                           FORMER NATIONATIONAL FELLOW AND EMERITUS SCIENTIST
                                 COLLEGE OF VETERINARY SCIENCE AND A H , JABALPUR 482001
                        drmcagrawal@gmail.com    www.indianschistosomiasis .blogspot.com
(Present address : ¾ Datt Arcade Phase Three, South Civil Lines, Jabalpur 482001)
Those who are working on diagnosis of schistosomiasis are aware how vast is the subject and its impossible for anyone to cover the topic in one hour lecture. Therefore, it will not be my goal to cover the whole subject , rather I will discussion some pertinent points on the topic at this occasion. We have discussed in detail about the diagnosis of schistosomiasis – both parasitological and immuno-diagnosis in our recently launched book(Agrawal,2012)  ,Schistosomes and schistosomiasis in South Asia (ISBN  9788132205388 www.springer.com) and you may refer this book for all the detailed information and related discussion . One advice is to those scientists who are interested to work on any problem of schistosomiasis in south Asia is to study well all the concerned  literature on the subject (as it is too vast ) prior undertaking any work as this prior study will inform them about the  work already done and the existing problems; such exercise will avoid duplication of work and will help in understanding well the present problem related to south Asian schistosomes and schistosomiasis which are certainly different from African or East Asian schistosomiasis .
Generally we are working and  discussing methodology of one or other diagnostic technique , its sensitivity and specificity , but there are no discussions whether  we need to devote our time , energy and funds for developing that  specific diagnostic technique and what will be its utility in present scenario. I think such discussion is necessary and my this lecture will focus on this topic while discussing schistosome diagnosis.
Further, by definition- as per Oxford dictionary , diagnosis means  “ statement of  nature of a disease or other condition made after observing its signs and symptoms” . Thus strictly diagnosis was restricted to what we call clinical diagnosis and as you know with passage of time it has gone in the back ground and laboratory diagnosis has taken a central stage-so is the case with schistosomiasis .One reason for this is our realization of difficulty in identifying the disease on symptoms alone due to commonness of them  in many other ailments. Therefore, we cannot whisk away laboratory diagnosis and in fact this is the main topic while discussing schistosomiasis diagnosis.  To this , I have taken liberty to include identifying schistosome infection in snail host ,as well- this is to understand the subject and related problems quite well.  
OUR AIM OF DIAGNOSIS : The basic question is what is our aim of identifying schistosome infection ? Whether it is only for treating a particular animal coming to veterinary hospital ? Or to declare a geographical area endemic with a given schistosome species ? Or to understand epizootiology of the infection ? Or to study zoonotic aspect of a schistosome species ? Or to know percentage of infected animals in each species ,age and sex wise ? Or to study immune status of animals after vaccination program ( so far ,no commercial vaccine is used against schistosomiasis in India ; it may be only on experimental basis ) . Or we wish to collect schistosomes during necropsy or in experimental animals for molecular and other studies  . Again schistosomiasis is existing in animals in two important forms (nasal schistosomiasis or snoring disease and hepato-intestinal schistosomiasis ) and diagnosis of both are different . So, there are varied aims of diagnosis hence our methodology of diagnosis should also differ as per our aim . Therefore, I will discuss the subject as per our aims and what best methodology we should follow to attain our aims of studies.
SENSITIVITY AND SPECIFICITY OF TESTS :
While starting the discussion, let me clarify that diagnosis of schistosomiasis is difficult due to two reasons . First, the symptoms in hepatic form like diarrhea, dysentery, anorexia, weakness, bottle jaw  etc are also present in other chronic or sub-acute infections . However, in snoring disease , the animal exhibits pathognomic signs like snoring sound, nasal discharge and nasal granuloma but totally depending on these symptoms may miss the infection in buffaloes or some cattle which are passing eggs in nasal discharge but without symptoms; and by this strategy , you cannot identify nasal schistosomiasis ,as is existing in Jabalpur , where local cattle are resistant to Schistosoma nasale but buffaloes are harboring the parasite- this  was confirmed by Banerjee and Agrawal (1991).
Therefore, for confirming the infection, we have to depend on laboratory diagnosis which is of two types –Parasitological and immunological- and both are having their own problems which have been discussed in chapter 7 and 8,respectively in above book. Basically , laboratory diagnosis is difficult due to poor sensitivity with no ante-mortem parasitological method being capable to correctly estimate schistosome prevalence in a given geographical area . For these reasons, I have argued about under estimation of schistosomiasis in whole of south Asia ( Agrawal, 1999)
 OUR PROBLEMS IN PARASITOLOGICAL METHODS
In parasitological diagnostic method , we can deal  only with  faeces (in hepatic form)  of the animal during ante-mortem  period . The most common method of faecal examination, followed in any veterinary diagnostic laboratory, is direct wet smear method . In some advance laboratories  sugar flotation or salt concentration method is also followed. Ideally , both supernatant and sediment should be examined for checking nematode and fluke infections but many times only supernatant is examined without caring for the sediment.  Ironically , examination of faeces by both these methods have resulted in identifying only 2-8% infection in any animal species whereas ,in reality , the infection rate was varying between 60-80% . Obviously, such diagnostic method cannot be recommended for diagnosing schistosomiasis when surveillance of the infection is our aim.
ANTEMORTEM DIAGNOSIS
Therefore, my laboratory assessed different coprological methods which may be used preferentially under field conditions. We have tried and compared direct smear, salt floatation,  acid-ether or formal-ether, sieving method, and Kato-katz methods in experimentally infected laboratory animals as well as  in field animals (Agrawal 2000 , Gupta 2002 , Vohra 2005  ). The results varied as per animal species, age of animal and intensity of the infection but sensitivity of these tests ascended from  direct smear to salt floatation, kato-katz , formal ether  methods leading highest level to 16% .
As any of the above egg detection method could not provide a practical solution of diagnostic problem, we tried hatching method by taking advantage that the eggs of schistosome species contain fully developed  miracidium , ready to hatch ,soon after coming in contact with  fresh water . There are many factors which influence this hatching of eggs and have been discussed elsewhere ( Agrawal,2012).
In summary , we can say that hatching method proved always superior over any egg detection method hence this is the test which we recommend to be followed in  field as well as in  research  laboratories. When we studied the method more meticulously , it was found more effective than any egg detection method where number of schistosome eggs in the faecal material was low- this is the young or old animals where egg concentration is low. For instance ,the hatching method ,though showed higher prevalence in pigs in comparison to egg detection methods, could not show significant variation in prevalence rate of porcine schistosomiasis at Jabalpur .This was because of higher faecal  concentration of schistosome eggs   in pigs (in comparison to other animal species) resulting its identification by other egg detection methods, as well.
The other  animal species where we observed different results, while comparing miracidia detection vis a vis egg detection , was experimentally infected albino mouse. Here, acid-ether method was more simple and sensitive than hatching method which failed many times to detect miracidia in the faecal material. 
The hatching method is not only simple but also cost effective as it does not require any chemical or use of micro slides. Therefore, this is an ideal method that can be followed under field conditions with little efforts . 
POST MORTEM METHODS :
Even diagnosing of schistosomiasis is not easy while conducting post mortem of an animal in comparison to other helminthic infections. Thus a simple cut in the liver may yield liver flukes, opening of rumen reveals amphistomes while intestine lumen will cause recovery of many nematode species . And in all these organs, you will not get schistosomes declaring the animal negative for schistosome infection. I may substantiate my statement by one reference of Rathor (1998) who compiled postmortem reports of more than eighteen thousand buffaloes of 28 livestock farms of India; the buffaloes were harboring Fasciola and amphistome infections but no case of schistosomiasis was recorded in these post mortem reports . As intermediate hosts of  amphistomes and schistosomes are identical ,it is difficult to believe that all the animals were negative for schistosomes-rather this is a case of failure of diagnosing schistosomiasis in any of these animals due to following routine post mortem techniques.  
This issue was attended by us and we have described specific techniques which should be followed during conducting post mortem of an animal for diagnosing schistosomiasis in them . These are two techniques ; one is perfusion technique for recovering alive blood flukes and the other is egg detection method using intestinal scrapings or liver pieces (Agrawal 2012, Vohra 2005  )    
IMMUNO-DIAGNOSIS :
A lot of research work  globally is being carried out on immuno-diagnosis mainly to study  human schistosomiasis in endemic countries and there are various reviews over the subject. It is difficult to cover them in one hour lecture . Nevertheless, I will mention some important facts which will help our discussion . For more details , you may read chapter 8 of the above referred book (Agrawal,2012).
ANTIBODY DETECTION METHODS :
In the beginning of the work, all the efforts were made to detect specific schistosome antibodies, developed by the host  due to schistosome pre- infection by using different types of the antigens .
There was fascination to use live larval stages of the blood flukes ,all three forms- viable eggs, miracidia, and cercariae- as experimental works have shown development of precipitates or blebs around viable schistosome eggs or immobilization of miracidia  or development of a hyaline membrane around cercariae when these larvae were immersed in the serum containing schistosome antibodies. The former two larvae were discarded as the tests were not very sensitive while CHR (cercarian hullen reaction ) proved a promising immunodiagnostic test though with the requirement of procuring alive cercariae for conducting the immunodiagnostic test.
To avoid the requirement of alive larvae, soluble antigens were developed using different methods and different stages of the schistosomes. Those who dealt the subject realized how difficult it is to recover a good quantity of schistosomes comparatively due to its smaller size and its location  in the blood vessels . Therefore, soon ,the immuno-diagnostic tests requiring larger quantity of antigens i.e. ring precipitation test were discarded . And in recent years ,all attention is diverted on ELISA ; as plate ELISA requires larger quantity of antigen and is more tedious , Dot ELISA is the method of choice among schistosomologists as each test requires only nano gram of antigens and is more simple to perform .
Looking to importance of diagnosis of fluke infections ,a NATP project was run by ICAR   with main center at  IVRI during 2000-2004 and  making Jabalpur, Hisar, as investigating centers for diagnosis of schistosomiasis ; some important work was also carried out at Bangalore veterinary college. Though these centers were able to develop Dot ELISA tests for diagnosing schistosomiasis with higher sensitivity , specificity could not reach to higher levels . Even some scientists ( Sumanth et al 2003) found  Dot ELISA positive in all the field animals who ever have been exposed to schistosome infections (?) and presently were either  negative or positive for schistosome eggs. What will be the utility of such diagnostic test in studying schistosomiasis remains debatable (Agrawal 2012).
ANTIGEN DETECTION METHOD :
The antibody detection methods have now been discarded globally by scientific community due to four  reasons. First , it does not differentiate between present and past infection . Second, it fails to calibrate intensity of the infection ; neither it reflects that all these positive animals are immune to re-infection . Third, it is difficult to collect blood from large animals under field conditions where controlling of the animals is a great problem (now there are ethical questions for collecting human blood merely for surveillance work). Fourth,the invasive method (collecting blood) merely for diagnosis is not favored due to the chances of transmitting viral and other infections; this has become more controversial in human cases where there are chances of transmitting HIV due to minor negligence of the technician.
Therefore, in recent years , attention has been diverted to detect schistosome antigen in faeces or urine of man and animals and principles of ELISA are followed for developing these methods. To make diagnostic test more specific and sensitive monoclonal antibodies have been used to attach them on nitrocellulose strip. Again , leading to  field adaptation of these tests , single step diagnostic kits have been developed where a solution is to pour on the strip which will develop two bands in case of positivity and only control band if the case is negative for schistosome infection.
Let me clarify that no commercial single step diagnostic kit is developed or available in India , though needed at least for diagnosing migratory human cases . This has been developed in some other countries  and one single step dipstick kit from European Veterinary Laboratory , Netherland was tried by us resulting in five positive human cases who were either suffering or were having history of cercarial dermatitis.
SCHISSTOSOMA SPECIFIC TESTS :
As this is the winter course on molecular studies on diagnosis and control of parasitic infections,  an important clarification , regarding all immuno-diagnostic methods is that they are capable to diagnose Schistosoma infection- only up-to genus level and none of these tests are species specific . Therefore, it is important to note that none of these tests will   inform which schistosome species is present in positive host species (in one sense , the test is good being able to be positive if the animal is infected by any schistosome species thus avoiding checking with many species specific tests- if and when developed  ). When it fails to identify schistosome species, any of these tests are of no use in identifying strains or sub-species of the schistosomes; neither they may help in detecting any new schistosome species.
Not only immuno-diagnostic methods, but our egg detection methods may fail to differentiate among schistosome species where egg morphology is closely resembling. If you study the literature, you will notice  that all  oval shaped schistosome eggs could not be ascribed to S.haematobium or S.indicum ; likewise , spindle shaped eggs does not mean only presence of S.spindale in the area ( Rollinson and Southgate 1987).
Therefore, now we have come to our main discussion –what is the aim of our diagnosis ?
It would have been clear from above discussion that the above methodology will not solve all our problems related to schistosomiasis and we have to stitch specific methods of diagnosis as per our requirements. I am discussing some of them in brief :
DIAGNOSIS FOR TREATMENT : When an animal with certain symptoms visit to a veterinary hospital , the main aim is the treatment of that particular animal. As the symptoms of schistosomiasis are common with other infections, though treatment is not the same, the differential diagnosis for schistosomiasis is important. The parasitological diagnostic tests have been termed as ‘Golden tests’  hence it is always recommended to diagnose these animals by coprological methods. This should include acid-ether or formal –ether method along with hatching method .The tests may be repeated twice or thrice if one time method shows negativity .
COLLECTION OF SCHISTOSOMES : If there is the need of collecting alive schistosomes from any animal species, perfusion method is the ideal one (Agrawal 2012). Recovery of schistosomes will also confirm presence of the infection in that particular host species and the geographical area to which the animal belonged  . In old days, the scientists teased the blood vessels for checking the animal positive for schistosomiasis and collecting alive blood – flukes; this method is tedious as well as less sensitive hence not recommended. Previously, it was difficult to apply perfusion technique as it was carried out by the use of a peristaltic pump which was costly and not available in Indian laboratories . however, we have replaced it  ,successfully, with a vertical water pump, most commonly used in desert coolers in Northern India (costing Rs 500/) hence now it is feasible to any laboratory to perform perfusion technique for recovering schistosomes during necropsy of the animals and the technique has been described in details in the book ( Agrawal,2012).
The alternative method, though less sensitive , is to collect mesentery or nasal cavity (when working on nasal schistosomiasis)  of the suspected animal, cut into small pieces and soak in Luke warm saline for 4-6 hours. Afterwards, the saline is filtered using a muslin cloth  which is transferred to  a petri-dish to collect the blood flukes ( Agrawal,2012).
IDENTIFYING NEW ENDEMIC AREA :  As you have come from different places of the country, it may be interesting for you to confirm whether a geographical area of your state or district or Tahseel is positive for any schistosome species. For confirming this possibility, you have to examine both intermediate and final hosts- in all seasons and in good number  else your results will not be reliable.
Till now only Indoplanorbis exustus and Lymnaea luteola have been identified as intermediate hosts for all the five well studied schistosome species i.e. Schistosoma indicum,S.spindale,S.nasale,S.incognitum and Orientobilharzia dattai while the snail host of Bivitellobilharzia nairi , O.bomfordi (?), S.haematobium (?- Gimvi infection) have still not been confirmed. Therefore, all the fresh water snails of the area should be examined meticulously for shedding of brevifurcated , apharyngeal ,non-ocillate  cercariae ; presence of such type cercariae will indicate prevalence of any mammalian schistosome species in the area (Agrawal,2012) .If these cercariae are shed by a new snail species, there are all chances that you are dealing with a new schistosome species .
As morphological studies of these cercariae cannot differentiate different mammalian schistosome species and certainly cannot confirm strains or sub-species of the schistosomes ,it is recommended to develop molecular techniques to study  these cercariae. So far, it is suggested that the snails are infected only with mono-species of fluke infections and molecular studies will be able to confirm or otherwise the above notion .
When you are examining final hosts for schistosome infection, first check if the animal is not a migratory animal otherwise origin of the infection will remain questionable. Therefore, area of birth of the animal is important in such studies and only by this methodology we suspected that Jabalpur is also harboring Schistosoma nasale in the buffaloes ( Banerjee and Agrawal 1991).
Though immuno-diagnostic methods are having high sensitivity (80-95%), their specificity ranks between 60-70% therefore solely depending on immuno-diagnosis while confirming a new endemic area is not a very good idea. However, not utilizing any immuno-diagnostic method may not reveal schistosome infection in a geographical area hence its use is important while exploring possibility of schistosomiasis in any animal species.  It must also be associated with sensitive parasitological methods which should always include hatching method. While examining animals for S.nasale ,instead of nasal discharge ,check the nasal scrapings as the latter is four  times more sensitive than the former method .
STUDYING ZOONOTIC POTENTIALS OF SCHISTOSOME SPECIES :  This is a topic of great interest in whole of South Asia but has not been studied meticulously . Identifying an endemic focus of urinary schistosomiasis in Gimvi village of Ratnagiri district, Maharashtra state ( Gadgil and Shah,1952) generated considerable interest in human schistosomiasis in the country but non –detection of clinical urinary cases from other parts of the country created a complacent view of absence of human schistosomiasis in other parts of the country . This view was developed ignoring the fact that S.incognitum was first detected in two human cases by Chandler (1926) and there are reports of finding schistosome eggs in human excreta in other parts of the country  (Agrawal,2012) . The topic has been discussed in more details while reviewing present status of schistosomiasis in India ( Agrawal,2005).  Prevalence of cercarial dermatitis in rural India is very common (Agrawal,2012) although no further studies have been carried out on the ailment. Thus we are not sure to what stage of development the schistosomula reaches in humans showing different immunological conditions  .
In the above cases, generally parasitological methods have failed to detect schistosome eggs in human excreta ,therefore, it is advocated to use a more sensitive and specific antigen detection test . The specificity of single step diagnostic kits , developed by using S.mansoni or S.haematobium, in other countries is not very high warranting developing such kits using Indian schistosome species.  Likewise, we do not have any specific immunological test for confirming cercarial dermatitis cases ; this is only history of dermatitis  and recovering schistosome cercariae from the fresh water snails which is collaborated with the ailment. Therefore, it will be beneficial to develop an immunodiagnostic test which may confirm cercarial dermatitis- ideally with possibility of differentiating cercarial dermatitis caused by avian schistosome cercariae and that by mammalian schistosome cercariae.
As you will notice that the single step diagnostic kit or immunodiagnostic test for cercarial dermatitis will not be able to identify schistosome species or strains involved in each case. Therefore, there is the need to develop molecular techniques for identifying species or hybrids or strains of schistosomes ,existing in whole of south Asia. Obviously, both the methodologies are supplementary to each one in solving the problem of schistosomiasis in the region.
CHECKING HOST  IMMUNITY AGAINST SCHISTOSOMES :  In viral and bacterial infections , immunological tests have also been used to check immune status of a given population and are good tools for vaccination programs . When we look the scenario with relation to schistosomiasis , two facts have emerged .
First, there is no vaccine which is being used for controlling schistosomiasis . This is the case both for human schistosomiasis as well as for animal schistosomiasis . More and more efforts are being made to develop a vaccine which may protect the host against schistosome infection. I am not aware if any institute in India is trying to develop a feasible vaccine for schistosome infection in any host species.
Secondly, our immuno-diagnostic tests are able to reveal presence of antibodies in positive cases but whether presence of these particular antibodies   will be able to protect the host against re-infection with schistosomes is questionable .So far , we have not developed any immuno-diagnostic test  whose positivity also guarantee protection of the host against re-infection.
SURVEILLANCE OF ANIMALS FOR SCHISTOSOMIASIS : Whenever , we undertake surveillance work for identifying any infection, our diagnostic test should be most sensitive and specific in diagnosing that infection. Ironically, no diagnostic test stands on above criteria with regards to schistosomiasis  . With Indian schistosomes , parasitological tests are least sensitive due to comparatively  lower egg excretion  hence their sole use in surveillance work is never advocated . In our opinion, hatching method has proved  most sensitive parasitological  method during ante-mortem hence must be included in all surveillance works. Those cases, positive by hatching method, must also be examined by a more sensitive egg detection method which will help  in identifying schistosome species of that area ,as well.
Since parasitological tests are least sensitive, the surveillance work must be carried out by supplementing parasitological methods with a more sensitive and specific immuno-diagnostic method. All the work , carried out in India, have proved Dot ELISA as most promising immuno-diagnostic test hence this should be incorporated in surveillance work but fully understanding its limitations (Agrawal,2012).
The antigen detection test in animal faeces will be more simple and be able to detect existing schistosome positive cases hence there is the need to develop these tests for understanding schistosomiasis in South Asia.
As we have already discussed the limitations of these immuno-diagnostic tests as well as those of parasitological tests, schistosomes and schistosomiasis cannot be understood well in whole of south Asia without developing more sophisticated molecular techniques which will help in identifying new schistosome species and also hybrids of the schistosomes which have developed in the continent due to hybridizations with existence of two or more schistosome species in a single host species. A collaboration with some international laboratories who are working on these topics since long  will make the efforts more easy ,accurate ,providing the results in shorter time frame .  
SUMMARY : The symptoms in hepatic schistosomiasis are vague hence laboratory diagnosis is carried out for confirmation of the disease. While deciding to employ diagnostic methodology, it is important to consider our aim of diagnosing the infection. When our sole aim is treating a sick animal, visiting a Veterinary Hospital ,coprological diagnosis is recommended but using more sensitive methods like acid-ether and hatching methods. During post-mortem ,either for collecting blood –flukes or for confirming the infection, perfusion method is the choice having highest sensitivity . In deciding zoonotic potentials of a given schistosome species or for surveillance of the infection  both parasitological and immunological methods should be followed as both will supplement each other. As antibody detection method does not differentiate between present and past infection with additional disadvantage of invasiveness, antigen detection methods in host’s excreta are gaining priorities .But it must be remembered that so far all immunodiagnostic methods are efficient only to identify the infection up-to genus level ( Schistosoma )  and cannot differentiate the infection  up-to species levels . Therefore, it is essential to undertake molecular  studies , if you wish to decide existence of schistosome species, sub-species or hybrids , in a given geographical area,   as no immuno-diagnostic method can reveal such complexities of schistosomiasis .
REFERENCES :
Agrawal, M.C. 1999. Schistosomosis : an underestimated problem in animals in South Asia. World Animal Review 92 : 55-57.
Agrawal, M.C. 2000. Final report on National Fellow project “Studies on strain identification,epidemiology,diagnosis,chemotherapy and zoonotic potentials of Indian schistosomes. ICAR, New Delhi
Agrawal,M.C. 2005. Present status of schistosomosis in India. Proc Nat Acad Sc, India. 75 (B),Special issue : 184-196
Agrawal MC.  2012.  Schistosomes and schistosomiasis in South Asia. Springer India Pvt Ltd , New Delhi
Banerjee PS and Agrawal MC.  1991.  Prevalence of Schistosoma nasale Rao 1933 at Jabalpur. Indian J Anim Sci 61 : 789-791
Chandler AC.  1926.  A new schistosome infection of man with note on other human fluke infections in India. Indian J Med Res 14 : 179-183
Gadgil RK and Shah SN.  1952 .  Human schistosomiasis in India. J Med Sci 6 : 760-763
Gupta S.  2002. Clinical, biochemical and parasitological studies and prevalence of caprine schistosomiasis in and around Jabalpur. Ph.D. Thesis, Rani Durgavati University, Jabalpur
Rollinson D and Southgate VR.  1987.  The genus Schistosoma : a taxonomic appraisal. In Rollinson D, Simpson AJG (eds) “The biology of schistosomes from genes to latrines “. Academic Press, London
Sumanth S ,D’Souza PE and Jagannath MS.  2003.  Immunodiagnosis of nasal and visceral schistosomiasis in cattle by Dot ELISA.Indian Vet J 80 :495-498

Vohra S.  2005.  Development of immunological methods for diagnosis of schistosomiasis in small ruminants. Ph.D Thesis. Jawaharlal Nehru Agriculture University, Jabalpur  

Friday, August 23, 2013

WHY THE BOOK SCHISTOSOMES AND SCHISTOSOMIASIS IN SOUTH ASIA

22nd August,2013
Sharon, MA ,USA

Work on schistosomiasis ,under tropical diseases, was  carried out since discovery of its etiological agent in 1851 by Theoder Bilharz .However, a great impetus was given to research in 1975 when World Health Organization took the disease in its umbrella under TDR program and encouraged scientists to find out effective diagnosis and treatment of the ailment . Sadly, no attention was paid on animal schistosomiasis except considering them as transmitters.
India was  the place where work on schistosomiasis was started in 1982 when Cobbold reported its presence in two bullocks in Calcutta and work continued ,thereafter.
I was trained by late Professor S C Dutt on Schistosomes in 1970s in the department of Parasitology, Veterinary College, Jawaharlal Nehru Agriculture University, Jabalpur hence I  decided to work on heterologous schistosome immunity  for my doctorate program and this was completed in 1978. During this period, I noticed every student in the department  is taking thesis problem on schistosome immunity by altering one or other parameter without having concern with other schistosome problems .Till that time,  nasal schistosomiasis was  considered main  problem, widely prevalent throughout India (an all India coordinated project on nasal schistosomiasis was operating in Chennai under late Dr VS Alwar)  while hepatic form was  neglected  with the presumption of its lower prevalence and minor pathology  . This neglect was based, wrongly , on the grounds that  Schistosoma incognitum  is non- pathogenic even to  its main host-pig , S.indicum causes liver nodules only in equines -the species having little social significance- while not much was known of S.spindale ,S.nairi,  Orientobilharzia dattai ,O. bomfordi .
Under these circumstances , I decided to understand Indian Schistosomes and schistosomiasis more comprehensibly by tackling different problems, related to it .Fortunately, Jabalpur is possessing  good slaughter houses- one for large animals and other for small animals- these greatly helped  my work.
Interest in schistosomiasis was fading in medical fraternity  assuming it a problem ,confined to Gimvi village of Ratnagiri district.  However,with advancing  the work, I developed the opinion, that it is not correct to consider man  refractory to  existing Indian species of Schistosomes as reports were coming of finding its eggs in man in some parts of the country. If we add hybridization and emergence of new strains/sub-species among Schistosomes, with  the possibility of lowering immune status of man due to  ailments like tuberculosis,HIV ,malnutrition ,it is unwise not to attend this problem  particularly when cercarial dermatitis was observed a common rural health problem all over India .
But, the greatest problem was lying in livestock industry where every domestic species ,in every state of India, was found infected with one or other schistosome species ,causing not only production losses but considerable mortality.  Outbreaks due to schistosomiasis were recorded in cattle and sheep , leading to 50% mortality -a great loss by all means . Even sudden death was recorded in piglets due to immature Schistosomes refuting earlier reports.  Obviously, the  question was why previous workers could not appreciate the problem (hepatic form) or why it is neglected by the field veterinarians. A simple answer emerged in the way of diagnosing hepatic schistosomiasis ; its symptoms (diarrhea, dysentery, anemia ,bottle jaw ,weight loss etc) are non-specific and fecal examination (direct smear or salt flotation ) did not reveal schistosome eggs . We showed that such fecal examination may reveal only 1-2% infections (hatching method 8-20%) while in realty the prevalence rate might be 70-90% . The routine post-mortem also fails to recover blood flukes from dead animals. This prompted me to write how hepatic schistosomiasis has been underestimated in whole of South Asia .To complicate present problem, Praziquentel, the trusted drug,  is not only expensive but proved not significantly effective against Indian schistosomes . There were  other problems also  in dealing schistosomiasis. In short :-
  • Its intriguing that  international Schistosome laboratories are located in some European countries with absence of the infection ,while India with maximum mammalian schistosome species, has no such facility thereby curtailing research funding and man power .
  • No data on schistosomiasis could be obtained from State Veterinary Departments or Central Government , as it is not compiled at any level .
  • Analysis of  patient record sheet in veterinary hospitals for occurrence of schistosomiasis or any disease for that matter, is difficult due to faulty recording and required changes .
  • Research on schistosomiasis required development of more accurate and specific techniques . We  developed techniques for breeding snails in large number, infecting them and animals. recovering flukes by new methods of perfusion technique etc which may be followed by any laboratory with minimum finances.
  •  Ironically ,it is the poor, rural persons who  are suffering most  in both ways- himself and because of his animals- and they have least to say in policy matters.
  • So far,  only human schistosomiasis is paid due  attention .Why animal schistosomiasis is neglected globally though it is causing considerable animal losses-so important to poor  rural persons.
  • Though work on schistosomes and schistosomiasis was being carried out in whole of South Asia since more than 100 years, yet there was no book on this topic.
What is the way out to attract attention of international scientists, administrators ,policy makers on Schistosomes and schistosomiasis of this region for a scientist with no political or financial clout ? Particularly when he is presuming same happenings in other infected African and Asian countries  ? The best way was to write a book covering all these and  other aspects and this  is what exactly I did.  I selected a global publisher Springer who came forward to spread my message in the book form (ISBN 9788132205388) and the book is available in every country (www.springer.com)  . I am confident that this book will be of tremendous help to all as it not only contains enormous information on Schistosomes and schistosomiasis of South Asia but also a critical analysis and dealing pertinent problems I am not aware if there is any other book on Veterinary schistosomiasis dealing any other geographical region (please inform,if any). It will be my pleasure if any  Government ,Organisation, University of any country is willing to take my services for understanding schistosomiasis in their country so that the infection may be understood well in that country.

Monday, July 15, 2013

Brief Personal Information



1. Name : Dr M.C. Agrawal,
2. Date of Birth : 2nd January, 1943, Firozabad, U.P.
3. Nationality : Indian
4. Address : Dr MAHESH CHANDRA AGRAWAL
¾,Datt Arcade Phase Three
South Civil Lines, JABALPUR 482001, Madhya Pradesh (India)
Phone : +91-761-2621772 (R) Mobile +91-9993224849
E-mail : drmcagrawal@gmail.com, mcagrawal@yahoo.com


Academic Qualifications.

1. 1st B.V.Sc. & A.H. 1964 I J.N.K.V.V. Jabalpur -
2. 2nd B.V.Sc. & A.H. 1965 I* - J.N.K.V.V. Jabalpur -
3 3nd B.V.Sc. & A.H. 1966 I* - J.N.K.V.V. Jabalpur -
4. Final B.V.Sc & A.H. 1967 I* - J.N.K.V.V. Jabalpur -
5 M.V.Sc 1974 I* J.N.K.V.V. Jabalpur
Major Parasitology : Minors Pathology, Microbiology
6 Ph. D. 1978 I* J.N.K.V.V Jabalpur
Major Parasitology : Minors Pharmacology, Biochemistry
5. M.V.Sc (Hons
--------------------------------------------------------------------------------------------
· Placed first in order of merit in the University ( J.N .Agriculture University).

Awards.


1. Emeritus Scientist Award of Indian Council of Agricultural Research (ICAR) ,New Delhi , 2005
1. Fellow of National Academy of Veterinary Sciences (India). - 1997
2. Fellow of Indian Association for Advancement of Veterinary Parasitology-2003
3. Fellow of Zoological Society of India (ZSI). - 1998
4. Dr G.D.Bhalerao memorial Gold medal of ZSI in 1998
5. I.C.A.R. National Fellow Award. Jan,1995
6. Prof. B.V.Rao Gold medal award 1991 of Indian Veterinary Association
7. Research Fellowship of ICAR for Ph.D. in 1974
8. University Gold Medal for first in order of merit in B.V.Sc & A.H ,1967
9. University Gold Medal for first in order of merit in M.V.Sc. Examination.1974
10. Certificates of Honors in M.V.Sc. 1974
11. Certificate of Honors in Ph.D.1978
12. Certificate of best student of the College.1967
13. First prize from ICAR, New Delhi. 1967
14. First prize from CAB Surrey, United Kingdom.1967
15. Dr SC Parija oration award of Indian Academy of Tropical Parasitology-2012


Appointments.

Member ,Board of Management, Kamdhenu Chattisgarh University,Durg Since June 2013
Emeritus Scientist,ICAR. Jawaharlal Nehru Krishi Vishwa Vidyalaya,Jabalpur 1/8/05-31/7/07
Dean College of veterinary Science & A.H. JN Agri University Jabalpur 1-10-2003- 31.1.2005
Professor & Head Department of Parasitology 29-12-2001-31.1.2005
Professor Department of Parasitology 28.7.1998-31.1.2005
National Fellow- Deptt. of Parasitology Vety.College Jabalpur 12.01.95 - 31.7.2000.
Professor & Head Deptt.of Vety.Parasitology CCSHAU,Hisar - 28.09.94 -09.01.95
Associate Prof./ Scientist Deptt.of Parasitology, Vety. College, Jabalpur 05.12.84 -27.09.94
Assistant Prof. Deptt. of Parasitology, Vety. College, Jabalpur01.01.73 -04.12.84
S.R.A./Demonstrator Deptt. of Parasitology, Vety. College, Jabalpur 15.01.68 -31.12.72
Vety.Assist. Surgeon. Deptt. of Animal Husbandry. Govt. of U.P.Lucknow 22.08.67-10.01.68

Experiences.


1. Teaching UG and Guiding postgraduates (M.V.Sc. & Ph.D.) for their theses in Vety Parasitology / Zoology / Life Sciences.
2. External and Internal Examiner of various Universities including I.V.R.I.
3. Short term courses for field Veterinarians.
4. Had been major Advisor for 6 Ph.D. and 5 M.V.Sc. theses and minor advisor for several theses.
5. Administrative experience as Dean of the Veterinary College (including planning for new veterinary college as per VCI norms) and running several ICAR research schemes.

Research.


1. Collaborated with Professor of Parasitology (Dr. M.Sano) Hamamatsu University School of Medicine, Japan under JSPS and INSA for work on epidemiology, chemotherapy and diagnosis of schistosomiasis (15.10.89 to 17.11.89 and 17.10.91 to 4.11.91)
2. Meeting with World Bank team at Bhopal with regard to spread of schistosomiasis through Narmada Valley Project.
3. Special Invitee in the National meeting on schistosomiasis held on 22.11.85 in National Institute of Communicable Diseases, Delhi.
4. Referee : of various scientific journals.
5. Co-Chairman/Reporter : in different scientific conferences including Asian Congress.
6. Reviewer : of research projects of ICAR and ICMR.
7. Member , Editorial Board, Journal of Parasitic Diseases, Journal of Veterinary Parasitology
8. Lead Papers : In Scientific Congresses, including Global Meet on Parasitic diseases.
9. Lectures : Delivered during various advance courses/ symposia/under UGC program.
10. Visiting scientist to Centre de biologie, University of Perpignan, France from 26th nov to 3rd Dec,2001 for discussion on schistosomes and schistosomiasis
11. Supervisor/Inspector for Veterinary Council of India, New Delhi

Research Schmes Handled.

1. Principal Investigator : Zoonotic potentials, Zooprophylaxis serodiagnosis and quick identification of cercariae of some mammalian schistosomes of Indian origin. I.C.M.R., New Delhi from 1.7.82 to 30.6.85
2. Supervisor : Development of Schistosoma spindale and S.indicum in laboratory and their diagnosis in final hosts. I.C.M.R., New Delhi from 18.2.87 to 17.2.90.
3. Parasitologist/Scientist : Sarcocystis and sarcocystosis in goats. Indian Council of Agriculture Research, New Delhi. 5.12.1984. 30.9.1987
4. National Fellow : Studies on strain identification, epidemiology, diagnosis, chemotherapy and zoonotic potentials of Indian schistosomes .Sponsored by ICAR, New Delhi from. 12.1.95 to 31.7.2000
5. Principal Investigator (collaborating center) Diagnosis of parasitic diseases of domestic animals. NATP-Mission mode, ICAR project from 1.7.2000 to 31.12.2004
6. Emeritus Scientist. Control of schistosomiasis under field conditions. Indian Council of Agriculture Research , New Delhi 1st Aug 2005 to 31st July 2007.

Present interests.

To investigate schistosomiasis / helminthic diseases/helminthic zoonosis in new geographical areas/ tribal population ; Dealing with wild life parasitic diseases; diagnosis and treatment of schistosomiasis/helminthic diseases ; guidance for new Veterinary college ; Establishment of new research laboratory for biological work/ to assist NGO/any other organization in public health related problems / preparation of scientific reports related to parasitic diseases/ public health related issues.
 
Books Published :
M C Agrawal (editor) 2002. Remembering Dr S C Dutt : The Parasitologist. Department of Parasitology,College of Veterinary Science and AH, Jawaharlal Nehru Krishi Vishwa Vidyalaya, Jabalpur MP
 
M C Agrawal  2012. Schistosomes and Schistosomiasis in South Asia. Springer India Private Limited, New Delhi . Page 351
 
Under Preparation
Research as a career in Parasitology

Research Publications :
 Books-2 ; Book chapters - 4 ; Research Review Papers -12 ; Research papers-110 ; Papers in Scientific conferences -53 ;Technical Reports-17 ;Scientific lectures delivered -13
 
My Blogs :
 
 
3.www.indianparasitologist.blogspot.com
 
4. A letter from USA ( www.dragrawalfromboston.blogspot.com )
 

.

Research for award of only doctorate degree

In a TV news today, on 14th July,2013 , the chief Minister of Gujarat ,Mr Narendra Modi has emphasized the need of linking research with Agriculture production in the country. He has blamed that research in India is merely to award Ph.D degree to the research student with no other utility.
 
It's difficult  to disagree with him with regards to present situation of research in the country-may be in Agriculture or any other field . Keep aside the research conducted by Ph.D scholars, even the work of established scientists are  not cared by any organization-either government (both state and Centre) or private one.- even where government has spent lot of money to carry out the research in that field. It will be better to substantiate my statement with the facts.
 
The premier organization of Agricultural research of the country, Indian Council of Agricultural Research , awarded National Fellowship in the year 1995 to the undersigned to work on animal schistosomiasis -a disease silently killing our domestic animals or causing production losses in whole of the country. This project was sanctioned with staff , research fellows and some important equipments.
 
The whole man power worked seriously on this disease continuously for nine years and published good number of research papers highlighting some new diagnostic methods and also about the future  problems which should be tackled to get rid of the problem from our animal industry; also what measures to be followed to protect man from this infection (schistosomiasis is a zoonotic disease)   . The work on the disease has been carried out in the country since last one hundred years ;some other institutes were also working on the infection and many research theses have been produced on this subject.. 
 
As there was no book on the subject I worked hard and the book on the topic " Schistosomes and schistosomiasis in South Asia" was published by Springer India Pvt Ltd in 2012 for the benefit of scientific community as well as for our administrators .
 
The crux of the problem is that no one- neither  Indian Council of Agriculture Research nor state or central government has ever tried to contact me to solve the problem in any geographical area- the problem of schistosomiasis  is still  existing with same  vigor  and hurdles and no one is interested to consult the expert for implementing or even verifying the new innovations. It appears that all our reports have been dumped in the files with no one caring to check what has been done in the country on a particular subject.
 
Thus , it appears that research in India is not for the benefit of its masses but only for award of Ph.D or only for "swant sukhaya".

Sunday, May 26, 2013

changing trends in research in Parasitology

India, being a tropical country, is a playground for myriads of parasites of men, animals and plants. Biologists with different specializations are engaged to solve the problems of parasitic infections. As usual, the initial attempts were for elucidating life cycle of the parasites, knowing their host range , distribution of the parasites in biotic and abiotic agencies . Since identification of the parasite was a pre-requisite for such research, taxonomic work dominated the scenario. So much so, that a little morphological difference led to creation of a new parasitic species without ascertaining other details. Even recovery of the parasite from a new host species or geographical area resulted in creation of a new parasite species. In late sixties, scientists concentrated their attention on pathology of parasitic diseases of the animals where histopathology was the dominant field. Finding of new drugs for the parasitic infections was another emerging field. Slaughter house material was important source to diagnose the infection or to judge prevalence of the infection in a given area. Parasitological diagnosis was the only way for identifying the infection during ante mortem. In early nineties , more changes were visible in the research in Veterinary Parasitology. Work was initiated to study clinical picture of important parasitic diseases. This time , more attention was paid on understanding a parasitic disease rather than parasitological findings. This period also witnessed start of studies on biochemical changes during parasitic diseases. This methodology was able to monitor the changes in the patients through out the disease period which was not the case with histopathology. Additionally , the biochemical changes helped in supplementing the treatment with desired drugs and also suggested prognosis of the infection. Thus we observed in our experimental schistosome infection in rabbits and goats that the animals suffered from severe anemia and hypoglycemia just after 30 days post infection and after wards which may lead to death of the animal if not treated. Poor efficacy of Parasitological methods in diagnosing parasitic infections was soon realized which resulted in two diversions. In the first , comparative studies were made for checking efficacy of different Parasitological methods at different stages of the parasitic infections and in different animal species. The other diversion was towards immuno-diagnosis. Here immuno-diagnosis of helminthic diseases was marred with the problems of non specific reactions because of poor quality of the antigen. There was also problem in procuring antigens in sufficient quantities as methods of in vitro cultivation of the parasites are not feasible in most of the cases. Initially, the work was conducted on old immunodiagnostic methods like CFT, IHA, DID etc but soon it was realized that the tests were not only non-specific but also required larger quantities of the antigen and serum. For this reason, the efforts were shifted to plate ELISA or dot ELISA –the latter is not only simple (without requiring any sophisticated equipments ) but also require little quantity of the antigen and test serum. Since antibody detection does not represent correct status of the infection in the host ,the work has been shifted , in recent years, for detecting circulating antigens rather than the antibodies. The advancement of parasitic work also emphasized the need of development of new techniques or modifications of old techniques for getting more accurate results. For instance, experimental work on schistosomes required breeding ,maintaining and infecting fresh water snails in the laboratory. The old methods were tedious, time consuming ,causing heavy snail mortality and may not be carried out at large scale. Like wise, there was no effective method of infecting domestic animal with schistosome cercariae or recovering schistosomes from them. The old methods were not accurate and blood fluke recovery was also not proper by tissue chopping method. Looking to the shortcomings of old methods , new techniques were developed in our laboratory. The polythene –tail technique proved accurate in infecting large animals with counted number of schistosome cercariae . A perfusion technique using vertical water pump, commonly used in the desert water coolers, made the technique cost effective , simple to be followed in any laboratory for more accurate schistosome recovery. There is a long debate about the scientific achievements by Indian scientists or Parasitologists. Most of the time, Indian work has been blamed a copycat of western work with little originality. However, it is necessary to implement this work under Indian conditions which is to be tested under Indian conditions. Perhaps, this research is fulfilling such need. Though its true that such scientific research do not get recognition at any level. Another debate has been initiated , in recent years, mainly by our public representatives who abandon all such type of research which does not solve the problems of general public . In their opinion, our money and efforts should be diverted to search the problems of general public . In relation to public health, there is emphasis to develop a simple field oriented diagnostic technique for an infectious disease Likewise, there is a need of finding a cost effective treatment strategy for important infectious diseases. We should not over emphasize Allopathic method of treating the ailments which are costly and marred with corporate biasness. Rather there is the need of searching our herbs for curing or preventing the diseases. In a recent national conference of parasitology at Regional Medical Research Centre for Tribes, Jabalpur , a Homeopathy college proprietor informed about the development of a homeopathic drug, costing less than one rupee per treatment, which is able to prevent malaria occurrence in the person for more than six months by a single dose therapy. He invited scientific community to verify this claim and if found true to extend it in other geographies . Certainly, there is need not to discard such claims without verifications and to concentrate more attention on alternate methodology which is cost effective and is able to solve our public health problems. It should also be remembered that 90% countries ,facing public health problems like ours , are poor and will be more than happy to try whatever India may develop to solve such health problems.