Survey of domestic cattle for anti-Leishmania antibodies and Leishmania DNA in a visceral leishmaniasis endemic area of Bangladesh

Full metadata record
DC FieldValueLanguage
dc.contributor.authorAlam, Mohammad Shafiul-
dc.contributor.authorGhosh, Debashis-
dc.contributor.authorKhan, Md Gulam Musawwir-
dc.contributor.authorIslam, Mohammad Faizul-
dc.contributor.authorMondal, Dinesh-
dc.contributor.authorItoh, Makoto-
dc.contributor.authorIslam, Md Nurul-
dc.contributor.authorHaque, Rashidul-
dc.date.accessioned2016-05-22T03:44:10Z-
dc.date.available2016-05-22T03:44:10Z-
dc.date.issued2011-
dc.identifier.citationBMC Vet Res 2011 Jun 8;7(1):27en_US
dc.identifier.urihttp://dspace.icddrb.org:8080/jspui/handle/123456789/6200-
dc.description.abstractBackground: Visceral leishmaniasis (VL), caused by an intracellular parasite Leishmania donovani in the Indian subcontinent, is considered to be anthroponotic. The role of domestic animals in its transmission is still unclear. Although cattle are the preferred blood host for Phlebotomus argentipes, the sandfly vector of VL in the Indian subcontinent, very little information is available for their role in the disease transmission. In this study, we examined domestic cattle for serological and molecular evidence of Leishmania infection in a VL-endemic area in Bangladesh. Blood samples from 138 domestic cattle were collected from houses with active or recently-treated VL and post-kala-azar dermal leishmaniasis patients. The presence of anti-leishmanial antibodies in serum was investigated using enzyme-linked immunosorbent assay (ELISA) and then with direct agglutination tests (DAT). Nested PCR (Ln PCR) was performed to amplify the ssu-rRNA gene using the DNA extracted from Buffy coat. Recently-developed molecular assay loop-mediated isothermal amplification (LAMP) was also performed for further sensitive detection of parasite DNA. Results: In this study, 9.4% (n = 13) of the cattle were found to be positive by ELISA. Of the 13 ELISA-positive cattle, only four (30.8%) were positive in DAT. Parasite DNA was not detected in either of the molecular assays (Ln PCR and LAMP). Conclusions: The study confirmed the presence of antibodies against Leishmania parasite in cattle. However, the absence of Leishmania DNA in the cattle indicates clearly that the cattle do not play a role as reservoir host. Similar study needs to be undertaken in the Indian subcontinent to determine the role of other domestic animals on which sandflies feed.en_US
dc.description.sponsorshipicddr,ben_US
dc.language.isoen_USen_US
dc.subjectAntibodies, Protozoanen_US
dc.subjectCattle diseasesen_US
dc.subjectLeishmania donovanien_US
dc.subjectLeishmaniasis, Visceralen_US
dc.titleSurvey of domestic cattle for anti-Leishmania antibodies and Leishmania DNA in a visceral leishmaniasis endemic area of Bangladeshen_US
dc.typeJournal articlesen_US
Appears in Collections:Scale-up

Files in This Item:
File Description SizeFormat 
2011---BMCVetRes---AlamMS---27.pdf3.07 MBAdobe PDFView/Open


This item is protected by original copyright