Insecticide Susceptibility of Phlebotomus argentipes in Visceral Leishmaniasis Endemic Districts in India and Nepal

Objectives To investigate the DDT and deltamethrin susceptibility of Phlebotomus argentipes, the vector of Leishmania donovani, responsible for visceral leishmaniasis (VL), in two countries (India and Nepal) with different histories of insecticide exposure. Methods Standard WHO testing procedures were applied using 4% DDT and 0.05% deltamethrin impregnated papers. The effect of the physiological status (fed and unfed) of females on the outcome of the bioassays was assessed and the optimal time of exposure for deltamethrin was evaluated on a colony population. Field populations from both countries were tested. Results Fed and unfed females responded in a similar way. For exposure time on field samples 60 min was adopted for both DDT and deltamethrin. In Bihar, knockdown and mortality with DDT was respectively 20 and 43%. In Nepal almost all sand flies were killed, except at the border with Bihar (mortality 62%). With 0.05% deltamethrin, between 96 and 100% of the sand flies were killed in both regions. Conclusions Based on literature and present data 4% DDT and 0.05% deltamethrin seem to be acceptable discriminating concentrations to separate resistant from susceptible populations. Resistance to DDT was confirmed in Bihar and in a border village of Nepal, but the sand flies were still susceptible in villages more inside Nepal where only synthetic pyrethroids are used for indoor spraying. The low effectiveness of indoor spraying with DDT in Bihar to control VL can be partially explained by this resistance hence other classes of insecticides should be tested. In both countries P. argentipes sand flies were susceptible to deltamethrin.

[1]  M. Coosemans,et al.  Development of an Enzyme-Linked Immunosorbent Assay to Identify Host-Feeding Preferences of Phlebotomus Species (Diptera: Psychodidae) in Endemic Foci of Visceral Leishmaniasis in Nepal , 2010, Journal of medical entomology.

[2]  S. Sundar,et al.  The epidemiology of Leishmania donovani infection in high transmission foci in India , 2010, Tropical medicine & international health : TM & IH.

[3]  F. Chappuis,et al.  Epidemiology of Leishmania donovani infection in high‐transmission foci in Nepal , 2010, Tropical medicine & international health : TM & IH.

[4]  M. Rowland,et al.  Effect of Village-wide Use of Long-Lasting Insecticidal Nets on Visceral Leishmaniasis Vectors in India and Nepal: A Cluster Randomized Trial , 2010, PLoS neglected tropical diseases.

[5]  N. F. Gontijo,et al.  Susceptibility to chemical insecticides of two Brazilian populations of the visceral leishmaniasis vector Lutzomyia longipalpis (Diptera: Psychodidae) , 2009, Tropical medicine & international health : TM & IH.

[6]  S. Kesari,et al.  A report on the indoor residual spraying (IRS) in the control of Phlebotomus argentipes, the vector of visceral leishmaniasis in Bihar (India): an initiative towards total elimination targeting 2015 (Series-1). , 2009, Journal of vector borne diseases.

[7]  David Weetman,et al.  Does kdr genotype predict insecticide-resistance phenotype in mosquitoes? , 2009, Trends in parasitology.

[8]  S. Sundar,et al.  Visceral Leishmaniasis Elimination Programme in India, Bangladesh, and Nepal: Reshaping the Case Finding/Case Management Strategy , 2009, PLoS neglected tropical diseases.

[9]  A. Joshi,et al.  An effectiveness of Insecticide spray in the control of visceral leishmaniasis in Nepal , 2008 .

[10]  R. Haque,et al.  Present situation of vector-control management in Bangladesh: a wake up call. , 2008, Health policy.

[11]  S. Sundar,et al.  Vector control by insecticide‐treated nets in the fight against visceral leishmaniasis in the Indian subcontinent, what is the evidence? , 2008, Tropical medicine & international health : TM & IH.

[12]  Niko Speybroeck,et al.  Long‐lasting insecticidal nets fail at household level to reduce abundance of sandfly vector Phlebotomus argentipes in treated houses in Bihar (India) , 2008, Tropical medicine & international health : TM & IH.

[13]  R L Gurubacharya,et al.  Prevalence of visceral leishmania & HIV co-infection in Nepal. , 2006, The Indian journal of medical research.

[14]  J. Hemingway,et al.  Molecular and biochemical characterization of a sand fly population from Sri Lanka: evidence for insecticide resistance due to altered esterases and insensitive acetylcholinesterase , 2005, Bulletin of Entomological Research.

[15]  P. Desjeux Leishmaniasis: current situation and new perspectives. , 2004, Comparative immunology, microbiology and infectious diseases.

[16]  M. Das,et al.  Epidemiological study of kala‐azar by direct agglutination test in two rural communities of eastern Nepal , 2004, Tropical medicine & international health : TM & IH.

[17]  S. Bhattacharya,et al.  Susceptibility of Phlebotomus argentipes against DDT in endemic Districts of North Bihar, India. , 2004, The Journal of communicable diseases.

[18]  M. Maroli,et al.  Control of phlebotomine sandflies , 2003, Medical and veterinary entomology.

[19]  R. Srinivasan,et al.  Susceptibility of Phlebotomus argentipes and P. papatasi (Diptera: Psychodidae) to insecticides. , 1999, The Journal of communicable diseases.

[20]  C S Swaminath,et al.  Transmission of Indian kala-azar to man by the bites of Phlebotomus argentipes, ann and brun. 1942. , 2006, The Indian journal of medical research.

[21]  S. Sharma,et al.  Resistance of sandflies to DDT in Kala-azar endemic districts of Bihar, India. , 2001, Bulletin of the World Health Organization.