Epidemiology of malaria transmission in forest and plain ecotype villages in Sundargarh District, Orissa, India

Transactions of the Royal Society of Tropical Medicine and Hygiene

Volumn 100, Issue 10, 2006, Pages 917-925

  Sharma, Surya K ^a   Tyagi, Prajesh K ^a   Padhan, Khageswar ^a   Upadhyay, Ashok K ^a   Haque, Mohammed A ^a   Nanda, Nutan ^a   Joshi, Hema ^a   Biswas, Sukla ^a   Adak, Tridibes ^a   Das, Bhawani S ^b   Chauhan, Virander S ^c   Chitnis, Chetan E ^c   Subbarao, Sarala K ^a,d  

^a NATIONAL INSTITUTE OF MALARIA RESEARCH   (India)

^b ISPAT GENERAL HOSPITAL   (India)

^c INTERNATIONAL CENTRE FOR GENETIC ENGINEERING AND BIOTECHNOLOGY ICGEB   (India)

^d INDIAN COUNCIL OF MEDICAL RESEARCH   (India)

Author keywords

Anopheles culicifacies; Anopheles fluviatilis; Entomological inoculation rate; India; Malaria; Plasmodium falciparum

Indexed keywords

CHLOROQUINE;

ADOLESCENT; ADULT; AGE; ANIMAL TISSUE; ANOPHELES; ARTICLE; CHILD; CONTROLLED STUDY; FEMALE; FOREST; GEOGRAPHY; HIGH RISK POPULATION; HUMAN; INCIDENCE; INDIA; INFANT; INFECTION PREVENTION; INFECTION RATE; INFECTION RISK; INSECT BITE; MAJOR CLINICAL STUDY; MALARIA; NONHUMAN; PARASITE TRANSMISSION; PARASITE VECTOR; PLASMODIUM FALCIPARUM; PRAIRIE; PREVALENCE; SEASONAL VARIATION;

ADOLESCENT; ADULT; AGED; ANIMALS; ANOPHELES; CHILD; CHILD, PRESCHOOL; CROSS-SECTIONAL STUDIES; HUMANS; INCIDENCE; INDIA; INFANT; INFANT, NEWBORN; INSECT VECTORS; LONGITUDINAL STUDIES; MALARIA, FALCIPARUM; MIDDLE AGED; PREVALENCE; RURAL HEALTH; SPLEEN;

ANOPHELES FLUVIATILIS; PLASMODIUM FALCIPARUM;

EID: 33746641805     PISSN: 00359203     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.trstmh.2006.01.007     Document Type: Article

References (37)

1. Baird J.K. Host age as a determinant of naturally acquired immunity to Plasmodium falciparum. Parasitol. Today 11 (1995) 105-111
2. Baird J.K., Jones T.R., Danudirgo E.W., Basri H., Anis B.A., Bangs M.J., Wiady I., and Masbar S. Age-dependent acquired immunity against Plasmodium falciparum among people with 2 years exposure to hyperendemic malaria. Am. J. Trop. Med. Hyg. 45 (1991) 65-76
3. Baird J.K., Sismadi P., Masbar S., Ramzan A., Purnomo B.W., Sekartuti, Tjitra E., Rumoko B.W., and Arbani P.R. A focus of endemic malaria in central Java. Am. J. Trop. Med. Hyg. 54 (1996) 98-104
4. Bruce-Chwatt L.J. A longitudinal survey of natural malaria infection in a group of West African adults. West Afr. Med. J. 12 (1963) 141-173
5. Burkot T.R., Zavala F., Gwadz R.W., Collins F.H., Nussenzweig R.S., and Roberts D.R. Identification of malaria-infected mosquitoes by a two-site enzyme-linked immunosorbent assay. Am. J. Trop. Med. Hyg. 33 (1984) 227-231
6. Chattopadhyay R., Sharma A., Srivastava V.K., Pati S.S., Sharma S.K., Das B.S., and Chitnis C.E. Plasmodium falciparum infection elicits both variant-specific and cross-reactive antibodies against parasite surface antigen variants. Infect. Immun. 71 (2003) 597-604
7. Collins R.Y., Dash B.K., Agarwala R.A., and Dhal K.B. An adaptation of gel diffusion technique for identifying the source of mosquito blood meals. Indian J. Malariol. 23 (1986) 81-89
8. Das B.S., Thurnham D.I., and Das D.B. Influence of malaria on markers of iron status in children: implications for interpreting iron status in malaria-endemic communities. Br. J. Nutr. 78 (1997) 751-760
9. Das B.S., Nanda N.K., Rath P.K., Satpathy R.N., and Das D.B. Anaemia in acute, Plasmodium falciparum malaria in children from Orissa state, India. Ann. Trop. Med. Parasitol. 93 (1999) 109-118
10. DeMaeyer E.M. Preventing and Controlling Iron Deficiency Anemia through Primary Health Care: a Guide for Health Administrators and Programme Managers (1989), World Health Organization, Geneva
11. Green C.A., and Hunt R.H. Interpretation of variation in ovarian polytene chromosomes of Anopheles funestus Giles, A. parensis Giles and A. aruni?. Genetica 51 (1980) 187-195
12. Gunasekaran K., Sahu S.S., Parida S.K., Sadanandane C., Jambulingam P., and Das P.K. Anopheline fauna of Koraput District, Orissa state with particular reference to transmission of malaria. Indian J. Malariol. 89 (1989) 340-343
13. Hay S.I., Roger D.J., Toomer J.F., and Snow R.W. Annual Plasmodium falciparum entomological inoculation rates (EIR) across Africa: literature survey, internet access and review. Trans. R. Soc. Trop. Med. Hyg. 94 (2000) 113-127
14. Jones T.R., Baird J.K., Bangs M.J., Annis B.A., Purnomo, Basri H., Gunawan S., Harjosuwarno S., McElroy P.D., and Hoffman S.L. Malaria vaccine study site in Irian Jaya, Indonesia: Plasmodium falciparum incidence measurements and epidemiologic considerations in sample size estimation. Am. J. Trop. Med. Hyg. 50 (1994) 210-218
15. Luxemburger C., Thwai K.L., White N.J., Webster H.K., Kyle D.E., and Maelan Kirri K. The epidemiology of malaria in a Karen population on the Western border of Thailand. Trans. R. Soc. Trop. Med. Hyg. 90 (1996) 105-111
16. Luxemburger C., Ricci F., Nosten F., Raimond D., Bather S., and White N.J. The epidemiology of severe malaria in an area of low transmission in Thailand. Trans. R. Soc. Trop. Med. Hyg. 91 (1997) 562-566
17. Marsh K., and Greenwood B.M. Malaria - a neglected disease?. Parasitology 104 Suppl. (1992) S53-S69
18. Mishra S.K., Mohanty S., and Das B.S. The influence of healthcare facilities on malarial mortality in and around Rourkela, India. Ann. Trop. Med. Parasitol. 96 (2002) 835-837
19. Parida S.K., Gunasekaran K., Sadanandane C., Patra K.P., Sahu S.S., and Jambulingam P. Infection rate and vectorial capacity of malaria vectors in Jeypore hill tract. Indian J. Malariol. 28 (1991) 207-213
20. Prusty S.K.R., and Das B.S. Low incidence of the severe complications of malaria and absence of malaria-specific mortality in Tensa, Sundargarh District, Orissa state, India, an area hyper-endemic for malaria. Ann. Trop. Med. Parasitol. 95 (2001) 133-140
21. Sharma V.P. Re-emergence of malaria in India. Indian J. Med. Res. 103 (1996) 26-45
22. Sharma S.K., Pradhan P., and Padhi D.M. Socio-economic factors associated with malaria in a tribal area of Orissa, India. Indian J. Public Health 45 (2001) 93-98
23. Sharma S.K., Chattopadhyay R., Chakrabarti K., Pati S.S., Srivastava V.K., Tyagi P.K., Mahanty S., Misra S.K., Adak T., Das B.S., and Chitnis C.E. Epidemiology of malaria transmission and development of natural immunity in a malaria-endemic village, San Dulakudar, in Orissa state, India. Am. J. Trop. Med. Hyg. 71 (2004) 457-465
24. Sharma S.K., Tyagi P.K., Padhan K., Adak T., and Subbarao S.K. Malarial morbidity in tribal communities living in the forest and plain ecotypes of Orissa, India. Ann. Trop. Med. Parasitol. 98 (2004) 459-468
25. Singh J., Ray A.P., and Nair C.P. JSB stain-its preparation in the powder form and the staining technique. Indian J. Malariol. 7 (1953) 267
26. Singh N., Mishra A.K., Chand S.K., and Sharma V.P. Population dynamics of Anopheles culicifacies and malaria in the tribal area of central India. J. Am. Mosq. Control Assoc. 15 (1999) 283-290
27. Singh N., Mishra A.K., Shukla M.M., and Chand S.K. Forest malaria in Chhindwara, Madhya Pradesh, central India: a case study in a tribal community. Am. J. Trop. Med. Hyg. 68 (2003) 602-607
28. Smith T., Beck H.P., Kitua A., Mwankusye S., Felger I., Fraser-Hurt N., Irion A., Alonso P., Teuscher T., and Tanner M. Age dependence of the multiplicity of Plasmodium falciparum infections and of other malariological indices in area of high endemicity. Trans. R. Soc. Trop. Med. Hyg. 93 Suppl. 1 (1999) 15-20
29. Snow R.W., Bastos de Azevedo I., Lowe B.S., Kabiru E.W., Nevill C.G., Mwankusye S., Kassiga G., Marsh K., and Teuscher T. Severe childhood malaria in two areas of markedly different falciparum transmission in east Africa. Acta Trop. 57 (1994) 289-300
30. Snow R.W., Guerra C.A., Noor A.M., Myint H.Y., and Hay S.I. The global distribution of clinical episodes of Plasmodium falciparum malaria. Nature 434 (2005) 214-217
31. Soe S., Aye K.S., Aung H., Win N., Aung T., Swe T., Roussilhon C., Perignon J.L., and Druilhe P. Premunition against Plasmodium falciparum in a malaria hyperendemic village in Myanmar. Trans. R. Soc. Trop. Med. Hyg. 95 (2001) 81-84
32. Subbarao, S.K., 1998. Anopheline species complexes in Southeast Asia. Regional Office for Southeast Asia, WHO Technical Publication, SEARO No. 18.
33. Subbarao S.K., Vasantha K., and Sharma V.P. Cytotaxonomy of malaria vectors in India. In: Service M.E. (Ed). Biosystematics of Haematophagous Insects. Systematics Association Special Volume 37 (1988), Clarendon Press, Oxford 25-37
34. Subbarao S.K., Vasantha K., Joshi H., Raghavendra K., Usha Devi C., Sathyanarayana T.S., Cochrane A.H., Nussenzweig R.S., and Sharma V.P. Role of Anopheles culicifacies sibling species in malaria transmission in Madhya Pradesh State, India. Trans. R. Soc. Trop. Med. Hyg. 86 (1992) 613-614
35. Subbarao S.K., Nanda N., Vasantha K., Dua V.K., Malhotra M.S., Yadav R.S., and Sharma V.P. Population cytogenetic evidence for three sibling species in Anopheles fluviatilis (Diptera: Culicidae). Ann. Entomol. Soc. Am. 87 (1994) 116-121
36. Trape J.F., Rogier C., Konatz L., Diagne N., Bouganali H., Canque B.C., Legros F., Badji A., Ndiaye G., Ndiaye P., Brahimi V., Faye O., Druilhe P., and Pereira da Silva L. The Dielmo Project: a longitudinal study of natural malaria infection in a community living in a holoendemic area of Senegal. Am. J. Trop. Med. Hyg. 51 (1994) 123-127
37. WHO, 1963. Terminology of Malaria and of Malaria Eradication. World Health Organization, Geneva, Monograph Series No. 13.