Respiratory illness in young and adult cattle caused by bovine viral diarrhea virus subgenotype 2b in singular and mixed bacterial infection in a BVDV-vaccinated dairy herd

被引:0
作者
Fritzen, Juliana Torres Tomazi [1 ]
Yasumitsu, Carolina Yuka [1 ]
Silva, Isabela Vaz [1 ]
Lorenzetti, Elis [1 ,2 ]
Alfieri, Alice Fernandes [1 ,3 ]
Alfieri, Amauri Alcindo [1 ,4 ]
机构
[1] Univ Estadual Londrina, Dept Prevent Vet Med, Lab Anim Virol, POB 10011, Celso Garcia Cid Rd, PR455 Km 380, BR-86057970 Londrina, PR, Brazil
[2] Univ Pitagoras Unopar, Post Grad Program Anim Hlth & Prod, Arapongas, PR, Brazil
[3] Univ Estadual Londrina, Dept Prevent Vet Med, Mol Biol Unit, Multiuser Anim Hlth Lab, Londrina, PR, Brazil
[4] Univ Estadual Londrina, Natl Inst Sci & Technol Dairy Prod Chain INCT LEIT, Dairy Prod Chain INCT Leite, Londrina, Brazil
关键词
Bovine respiratory disease; BVDV subgenotypes; Mycoplasma bovis; BVDV vaccine; Dairy cattle herd biosecurity; SEMI-NESTED PCR; GRANDE-DO-SUL; GENETIC-CHARACTERIZATION; PASTEURELLA-MULTOCIDA; ANTIGENIC DIVERSITY; RISK-FACTORS; DISEASE; CALVES; PATHOGENS; IDENTIFICATION;
D O I
10.1007/s42770-024-01476-x
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Bovine respiratory disease (BRD) is a common global health problem in dairy cattle. The definitive diagnosis of BRD is complex because its etiology involves several predisposing and determining factors. This report describes the etiology of a BRD outbreak in a dairy herd in the mesoregion of Central Eastern Paran & aacute;, which simultaneously affected young (calves and heifers) and adult (cows) Holstein-Friesian cattle. Nine biological samples, consisting of five lung samples from two cows and three suckling calves, and four nasal swab samples from heifers, were used for etiological diagnosis. The nucleic acids extracted from lung fragments and nasal swabs were subjected to PCR and RT-PCR assays for partial amplification of the genes of five viruses [bovine viral diarrhea virus (BVDV), bovine alphaherpesvirus 1 (BoAHV1), bovine respiratory syncytial virus (BRSV), bovine parainfluenza virus 3 (BPIV-3), and bovine coronavirus (BCoV)] and four bacteria (Mycoplasma bovis, Mannheimia haemolytica, Pasteurella multocida, and Histophilus somni) involved in the etiology of BRD. All nine biological samples from the animals with BRD tested negative for BoAHV1, BRSV, BPIV-3, BCoV, and H. somni. Therefore, the involvement of these microorganisms in the etiology of BRD outbreak can be ruled out. It was possible to identify the presence of BVDV and M. bovis in singular and mixed infections of the lower respiratory tract in cattle. BVDV was also identified in two nasal swabs: one as a single etiological agent and the other in association with two bacteria (P. multocida and M. haemolytica). The phylogenetic analysis conducted in the nucleotide sequence of the 5'UTR region and Npro gene of the BVDV amplicons demonstrated that the BVDV field strains of this BRD outbreak belong to subgenotype 2b. To the best of our knowledge, this is the first report of BVDV-2b involvement in the etiology of BRD in Brazil. Finally, it is necessary to highlight that the cattle were obtained from an open dairy herd with biannual vaccinations for BVDV-1a and - 2a.
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收藏
页码:4139 / 4146
页数:8
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