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Background: Globally, India has a high zoonotic disease burden and lacks surveillance data in humans and animals. Rodents are known reservoirs for many zoonotic diseases and their synanthropic behavior poses a great public health threat., Methods: In this study, trapped rodents/shrews from randomly selected villages within Puducherry, India, and their ectoparasites were screened for zoonotic pathogens, namely, Orientia tsutsugamushi, other pathogenic rickettsiae, Leptospira spp., Cryptosporidium spp., Coxiella burnetii and methicillin-resistant Staphylococcus aureus (MRSA) using conventional PCR. A total of 58 rodents/shrews were trapped from 11 villages. The species trapped were Suncus murinus (49/58, 84.48%), Rattus rattus (8/58, 13.79%) and Rattus norvegicus (1/58, 1.72%). All ectoparasites collected were identified as mites and its infestation rate was 46.55% (27/58)., Results: Real-time PCR targeting the 47 kDa gene of O. tsutsugamushi revealed positivity in one rodent and one shrew (3.45%) and two mite pools (7.41%). Conventional PCR targeting the 56 kDa gene revealed positivity in one shrew and two mite pools and the phylogenetic analysis of all three amplicons indicated the circulation of the Gilliam-related serotype. MRSA was detected in the alimentary tract of a shrew (1/32, 3.13%). Leptospira spp., Rickettsia, Cryptosporidium spp. and Co. burnetii tested negative., Conclusions: The detection of zoonotic pathogens within reservoir hosts and vectors poses a risk of transmission to humans. This study signifies the need for zoonotic pathogen surveillance in synanthropic rodents/shrews., (© The Author(s) 2024. Published by Oxford University Press on behalf of Royal Society of Tropical Medicine and Hygiene.)

The indirect fluorescent antibody technique was standardised for serodiagnosis of Cryptosporidiosis in naturally infected cattle. A total of 201 faecal and serum samples were collected from different farms, animal shelters and abbatoirs in and around Bangalore which included 11 samples positive for Cryptosporidium infection on faecal microscopy. Two species viz., Cryptosporidium parvum and Cryptosporidium andersoni were prevalent based on faecal examination. Oocysts were purified by using sedimentation and gradient centrifugation and then the samples were screened by immunofluorescence antibody technique (IFAT). Out of 201 sera samples 25 samples were positive for Cryptosporidial antibodies indicating an infection rate of 12.44%. [ABSTRACT FROM AUTHOR]