Rongguang Lu, Haixu Cao, Wei Yang, Jianhai Fu, Tingli Qian, Chengqi Zhang, Na Feng, Bo Hu, Liwen Xu, Shuangshuang Li, Guanyu Zhao, Qiumei Shi, Deyue Zang, Guobao Li, Xue Bai
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引用次数: 0
Abstract
Canine parvovirus (CPV) and canine enteric coronavirus (CCoV) are primary viral pathogens responsible for causing diarrhea in carnivores. CCoV infection generally induces mild enteritis, whereas infections solely by CPV or coinfections involving both CPV and CCoV frequently result in severe diarrhea and can lead to fatal outcomes in affected animals. This study investigated CPV and CCoV infections in raccoon dogs farmed in China between 2018 and 2023. Among the 133 small intestine tissue samples from raccoon dogs with severe diarrhea, 107 of 133 (80.5%) were CPV nucleic acid positive, involving CPV-2 and CPV-2a subtypes. The CPV-2 amplicons maintained I418T, S927A, and T27S. Moreover, the CPV-2a subtype amplicons possessed G300S, N562V, and Y573F mutations compared to dog-ori CPV-2a. Moreover, 30 of the 133 (22.6%) samples were positive for CCoV, containing the CCoV-IIa and CCoV-IIb subtypes. Of these, 25 of 30 (83.3%) samples were coinfected with CPV and CCoV. In CCoV infection alone, mild inflammatory infiltration was observed in the lamina propria of the small intestine. Immunohistochemical staining revealed that CCoV antigens were mainly detected in the crypts of the small intestine. Furthermore, coronavirus-like particles were observed in small intestine samples. Next, we analyzed the detailed binding model for raccoon dog-origin (RD-ori) CCoV-IIa with host aminopeptidase N (APN). The receptor-binding domain (RBD) of RD-ori CCoV-IIa showed robust binding to raccoon dog APN but not to human APN. Our results demonstrated that CPV-2a and CCoV are emerging in farmed raccoon dogs in northern China. Further investigations should be performed to monitor the potential evolution and recombination events of RD-ori CPV and CCoVs.
期刊介绍:
Transboundary and Emerging Diseases brings together in one place the latest research on infectious diseases considered to hold the greatest economic threat to animals and humans worldwide. The journal provides a venue for global research on their diagnosis, prevention and management, and for papers on public health, pathogenesis, epidemiology, statistical modeling, diagnostics, biosecurity issues, genomics, vaccine development and rapid communication of new outbreaks. Papers should include timely research approaches using state-of-the-art technologies. The editors encourage papers adopting a science-based approach on socio-economic and environmental factors influencing the management of the bio-security threat posed by these diseases, including risk analysis and disease spread modeling. Preference will be given to communications focusing on novel science-based approaches to controlling transboundary and emerging diseases. The following topics are generally considered out-of-scope, but decisions are made on a case-by-case basis (for example, studies on cryptic wildlife populations, and those on potential species extinctions):
Pathogen discovery: a common pathogen newly recognised in a specific country, or a new pathogen or genetic sequence for which there is little context about — or insights regarding — its emergence or spread.
Prevalence estimation surveys and risk factor studies based on survey (rather than longitudinal) methodology, except when such studies are unique. Surveys of knowledge, attitudes and practices are within scope.
Diagnostic test development if not accompanied by robust sensitivity and specificity estimation from field studies.
Studies focused only on laboratory methods in which relevance to disease emergence and spread is not obvious or can not be inferred (“pure research” type studies).
Narrative literature reviews which do not generate new knowledge. Systematic and scoping reviews, and meta-analyses are within scope.