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dc.contributor.authorShikha Rimalen_US
dc.contributor.authorKrishna Chandra Ojhaen_US
dc.contributor.authorWarangkhana Chaisowwongen_US
dc.contributor.authorYogendra Shahen_US
dc.contributor.authorDhan Kumar Panten_US
dc.contributor.authorAnucha Sirimalaisuwanen_US
dc.date.accessioned2020-10-14T08:23:39Z-
dc.date.available2020-10-14T08:23:39Z-
dc.date.issued2020-04-01en_US
dc.identifier.issn19326203en_US
dc.identifier.other2-s2.0-85083918733en_US
dc.identifier.other10.1371/journal.pone.0231967en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85083918733&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/70062-
dc.description.abstract© 2020 Rimal et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Background: Rabies is a vaccine-preventable neglected tropical viral zoonosis. It occurs worldwide, creating a very heavy burden in many developing countries, including Nepal. Dogs are the principle vector for the transmission of this disease in urban areas. Vaccination is the most important preventive measure in areas where dogs are the principle source of infection. This study was conducted with the aim of detecting virus-neutralising antibodies and associated factors against rabies in vaccinated household dogs of Kathmandu valley. Methods: Blood samples were collected from 110 vaccinated pet dogs in Kathmandu, Bhaktapur, and Lalitpur districts of Nepal. The samples were taken to the laboratory of the National Zoonosis and Food Hygiene Research Center where serum was separated. An indirect immune-enzymatic assay (PlateliaTM Rabies II kit ad usum Veterinarium, Biorad, China) was used for the detection of rabies virus anti-glycoprotein antibodies in the dog serum samples following the manufacturer's recommendations and instructions. Optical density values for unknown samples were compared with the positive sera titers in quantification tests obtained after a direct reading on the standard curve. Results were expressed as equivalent units per ml (EU/ml). Findings: Of the total samples, 89.09% exceeded the required seroconversion level (≥ 0.5 EU/ml); another 9.09% did not reach the seroconversion level (0.125-0.5 EU/ml); and 1.81% had undetectable seroconversion levels (<0.125 EU/ml) suggesting that the animal had not seroconverted according to the PLATELIA™ RABIES II test. Only one factor, the condition under which the dog was kept, was significantly associated with the antibody titer level. No association was found for any of the other factors included in the study. Interpretation Vaccination is the most effective measure for prevention and control of rabies. The locally manufactured brand of vaccine, which is available in Nepal, is potent enough to generate a sufficient amount of protective antibodies, equal to international brands.en_US
dc.subjectAgricultural and Biological Sciencesen_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectMultidisciplinaryen_US
dc.titleDetection of virus-neutralising antibodies and associated factors against rabies in the vaccinated household dogs of Kathmandu Valley, Nepalen_US
dc.typeJournalen_US
article.title.sourcetitlePLoS ONEen_US
article.volume15en_US
article.stream.affiliationsTribhuvan Universityen_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsNational Zoonoses and Food Hygiene Research Centreen_US
article.stream.affiliationsNational Academy of Medical Sciencesen_US
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