Molecular detection and pathological evaluation of Mesomycoplasma ovipneumoniae and its co-infecting agents in pneumonic goats of Akola district, India
6 affiliations
- 1MVSc Student, Department of Veterinary Pathology, Post Graduate Institute of Veterinary and Animal Sciences, Maharashtra Animal and Fishery Sciences University, Krushinagar, Akola, Maharashtra, India
- 2Department of Veterinary Pathology, Post Graduate Institute of Veterinary and Animal Sciences, Maharashtra Animal and Fishery Sciences University, Krushinagar, Akola, Maharashtra, India
- 3Department of Veterinary Microbiology, Post Graduate Institute of Veterinary and Animal Sciences, Maharashtra Animal and Fishery Sciences University, Krushinagar, Akola, Maharashtra, India
- 4Department of Veterinary Pharmacology and Toxicology, Post Graduate Institute of Veterinary and Animal Sciences, Maharashtra Animal and Fishery Sciences University, Krushinagar, Akola, Maharashtra, India
- 5Department of Poultry Science, Post Graduate Institute of Veterinary and Animal Sciences, Maharashtra Animal and Fishery Sciences University, Krushinagar, Akola, Maharashtra, India
- 6Department of Animal Nutrition, Post Graduate Institute of Veterinary and Animal Sciences, Maharashtra Animal and Fishery Sciences University, Krushinagar, Akola, Maharashtra, India
Abstract
Background:: M. ovipneumoniae is one of the pathogens responsible for chronic non-progressive pneumonia in sheep and goats. The pathogen disrupts mucociliary clearance and exacerbates disease severity through secondary infections.
Aims:: The present study aimed to investigate the occurrence of M. ovipneumoniae from pneumonic goats and to identify related pathomorphology.
Methods:: A total of 680 goat carcasses from Akola, Maharashtra, India, were examined. From these, 80 lung samples exhibiting pneumonia were collected, processed for M. ovipneumoniae confirmation and characterized for pulmonary lesions.
Results:: PCR analysis using genus specific primers identified Mycoplasma spp. in 35 cases (43.75%), while species specific primers targeting a fragment of the 16S rRNA gene confirmed M. ovipneumoniae in 24 cases (30%). Additionally, Mannheimia haemolytica and Pasteurella multocida were detected in 8 (33.33%, 8/24) and 3 (12.5%, 3/24) cases by employing PCR with 2 (8.33%, 2/24) cases exhibiting concurrent infection of all three pathogens, respectively. Five PCR amplicons of M. ovipneumoniae were subjected to phylogenetic analysis, confirming their clustering with other M. ovipneumoniae strains from India, USA and Turkey, while remaining distinct from other Mycoplasma spp. Histopathological analysis of M. ovipneumoniae positive lungs revealed bronchopneumonia (73.3%), broncho-interstitial pneumonia (13.3%) and interstitial pneumonia (26.66%). Characteristic lesions included fibrinous pleuritis, bronchiolar epithelial hyperplasia, necrotic alveolitis with type II pneumocyte hyperplasia, thickened interalveolar septa, syncytial cell formation and infiltration of inflammatory cells. Co-infections resulted in more severe lesions.
Conclusion:: The study confirmed the occurrence of M. ovipneumoniae in pneumonic goats from the region underscoring the need for large scale studies to understand its epidemiology.
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BibTeX
@article{kadam2026molecular,
title = {{Molecular detection and pathological evaluation of Mesomycoplasma ovipneumoniae and its co-infecting agents in pneumonic goats of Akola district, India}},
author = {N. Kadam and B. Kamdi and R. Ingole and S. Awandkar and S. Hajare and M. Wade and K. Deshpande},
journal = {Iranian Journal of Veterinary Research},
year = {2026},
month = aug,
doi = {10.22099/ijvr.2026.53925.8100},
url = {https://doi.org/10.22099/ijvr.2026.53925.8100},
note = {CC BY-NC-ND 4.0},
}
RIS
TY - JOUR
TI - Molecular detection and pathological evaluation of Mesomycoplasma ovipneumoniae and its co-infecting agents in pneumonic goats of Akola district, India
AU - N. Kadam
AU - B. Kamdi
AU - R. Ingole
AU - S. Awandkar
AU - S. Hajare
AU - M. Wade
AU - K. Deshpande
PY - 2026
DA - 2026/08/22
JO - Iranian Journal of Veterinary Research
DO - 10.22099/ijvr.2026.53925.8100
UR - https://doi.org/10.22099/ijvr.2026.53925.8100
AB - Background:: M. ovipneumoniae is one of the pathogens responsible for chronic non-progressive pneumonia in sheep and goats. The pathogen disrupts mucociliary clearance and exacerbates disease severity through secondary infections. Aims:: The present study aimed to investigate the occurrence of M. ovipneumoniae from pneumonic goats and to identify related pathomorphology. Methods:: A total of 680 goat carcasses from Akola, Maharashtra, India, were examined. From these, 80 lung samples exhibiting pneumonia were collected, processed for M. ovipneumoniae confirmation and characterized for pulmonary lesions. Results:: PCR analysis using genus specific primers identified Mycoplasma spp. in 35 cases (43.75%), while species specific primers targeting a fragment of the 16S rRNA gene confirmed M. ovipneumoniae in 24 cases (30%). Additionally, Mannheimia haemolytica and Pasteurella multocida were detected in 8 (33.33%, 8/24) and 3 (12.5%, 3/24) cases by employing PCR with 2 (8.33%, 2/24) cases exhibiting concurrent infection of all three pathogens, respectively. Five PCR amplicons of M. ovipneumoniae were subjected to phylogenetic analysis, confirming their clustering with other M. ovipneumoniae strains from India, USA and Turkey, while remaining distinct from other Mycoplasma spp. Histopathological analysis of M. ovipneumoniae positive lungs revealed bronchopneumonia (73.3%), broncho-interstitial pneumonia (13.3%) and interstitial pneumonia (26.66%). Characteristic lesions included fibrinous pleuritis, bronchiolar epithelial hyperplasia, necrotic alveolitis with type II pneumocyte hyperplasia, thickened interalveolar septa, syncytial cell formation and infiltration of inflammatory cells. Co-infections resulted in more severe lesions. Conclusion:: The study confirmed the occurrence of M. ovipneumoniae in pneumonic goats from the region underscoring the need for large scale studies to understand its epidemiology.
SN - 1728-1997
SN - 2252-0589
ER -