We monitored the prevalence of endoparasitic infections of rodents in Punjab State, India, between January 2004 and December 2005. Three species of wild rodents, namely the house rat, Rattus rattus (n = 42), the lesser bandicoot rat, Bandicota bengalensis (n = 34) and the Indian gerbil, Tatera indica (n = 15), were live-captured from houses and crop fields. Examination of various organs revealed that the highest rates of endoparasitic infection occurred in R. rattus (40.5%), followed by B. bengalensis (35.3 %) and then T. indica (20.0%), with an overall infection rate of 35.2%. All three rodent species were found naturally infected with one or more species of helminths. Metacestodes (1-6) of Cysticercus fasciolaris (larvae of Taenia taeniaeformis) were found in all three rodent species (in the liver). In one male T. indica, numerous robust T. taeniaeformis metacestodes were found in oval sacs attached to the mesentery and the abdominal wall, an unusual site. The cauda epididymal fluid of the same gerbil was also found to be infected with a very rare species of strongylid nematode, which could not be identified to genus or species level. It is possible that this nematode is transmitted sexually and thus may affect the reproductive potential of gerbils. This appears to be the first report of this phenomenon. In one B. bengalensis individual, the intestine was found to be obstructed with an acanthocephalan, Moniliformis moniliformis, with concurrent infection with C. fasciolaris in the form of multiple cysts in the liver. Although no natural protozoan infection was found in these field rodents, experimental Trypanosoma evansi infection has been established in all three species with high pathogenicity, and the possibility of sexual transmission was supported by the presence of T. evansi in the cauda epididymal fluid of male rats.
The direct agglutination test (DAT) has been assessed as a diagnostic procedure for visceral leishmaniasis. Fifty-six of 58 sera (96.5%) from confirmed cases of visceral leishmaniasis, whose bone marrow aspirates contained Leishmania donovani amastigotes, had agglutinating antibodies above the cut-off titre of 1:800. None of the sera from healthy control subjects from non-endemic or endemic areas had anti-leishmanial antibodies. Similarly, none of the sera obtained from cases of malaria or tuberculosis had agglutinating antibodies above the cut-off titre. A significant decline in agglutinating antibody titre in 3 cases following antileishmanial chemotherapy appeared to correlate with regression of clinical symptoms and the absence of amastigotes from bone marrow aspirates. One of 3 cases developed post-kala-azar dermal lesions and sera from this subject had an elevated agglutinating antibody titre. It is concluded that the DAT is a sensitive and specific test to confirm visceral leishmaniasis. As the formalin-fixed promastigotes, stained with Coomassie blue, which are used as antigen could be stored at 4 degrees C for 6 months without any loss of ability to detect anti-leishmanial antibodies, the DAT is recommended for use under field conditions.
Seven cloned lines of promastigotes of Leishmania donovani (UR 6) were isolated by limiting dilution. One clone, UR6-C25, failed to multiply inside the macrophages of line J774G8 and thus was labelled as avirulent. Another, UR6-C24, multiplied inside macrophages, had a virulence index as high as 93 +/- 9.8 and was thus labelled as highly virulent. The other five clones had variable degree of virulence indices ranging from 46.4 +/- 5.8 to 67.6 +/- 3.5. No significant difference in the degrees of attachment of virulent and avirulent populations of promastigotes to macrophages was observed, suggesting no difference in the ligand utilised by these populations for attachment to the macrophages. Acid phosphatase activity of cloned promastigotes correlated with the degree of virulence. These data suggest that acid phosphatase activity could be used as a marker to differentiate avirulent from virulent populations of promastigotes of L. donovani.
The aim of this study was to recommend locality-specific rodent pest management techniques for sugarcane using acute and anticoagulant rodenticides during the months when maximum damage is inflicted on the crop in Punjab, India. Sugarcane crops were found to be infested with four rodent species namely: Bandicota bengalensis (Gray and Hardwicke); Mus booduga (Gray); Millardia meltada (Gray) and Golunda ellioti (Gray), with B. bengalensis being the most prevalent species (accounting for 69.45-83.36% of the total catch). Surveys in 11 villages of three districts of Punjab (India) revealed 19.12 + 12.22% rodent damage to the sugarcane crop during the months of DecemberJanuary. Rodenticide treatments were conducted in farmer's fields in two districts of Punjab from December 2003 to January 2007. The results revealed that, to protect the sugarcane crop from rodent damage during the months of December-January, the rodenticide treatment may be applied either: (1) by double-baiting with 2% zinc phosphide followed by 0.005% bromadiolone after 15d at 1 kg/ha each, or (2) by single-baiting with 0.005% bromadiolone at 2 kg/ha. The impact of rodenticide treatment in canefields was also evident in the adjoining wheat crop fields where the incidence of rodent damage was less (0.97-3.24%) than in the fields surrounding untreated canefields (3.53-6.22%).
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