Fritzen Juliana Torres Tomazi, Yasumitsu Carolina Yuka, Silva Isabela Vaz, Lorenzetti Elis, Alfieri Alice Fernandes, Alfieri Amauri Alcindo
Laboratory of Animal Virology, Department of Preventive Veterinary Medicine, Universidade Estadual de Londrina, Celso Garcia Cid Road, PR455 Km 380, PO Box 10011, Londrina, Paraná, 86057-970, Brazil.
Post Graduate Program in Animal Health and Production, Universidade Pitágoras Unopar, Arapongas, Paraná, Brazil.
Braz J Microbiol. 2024 Dec;55(4):4139-4146. doi: 10.1007/s42770-024-01476-x. Epub 2024 Aug 15.
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 Paraná, 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 N 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.
牛呼吸道疾病(BRD)是奶牛中常见的全球性健康问题。BRD的确诊很复杂,因为其病因涉及多个易感因素和决定因素。本报告描述了巴拉那州中东部中区域一个奶牛群中BRD疫情的病因,该疫情同时影响了年轻(犊牛和小母牛)和成年(母牛)的荷斯坦 - 弗里生奶牛。九个生物样本用于病因诊断,其中包括来自两头母牛和三头哺乳犊牛的五个肺样本,以及来自小母牛的四个鼻拭子样本。从肺组织碎片和鼻拭子中提取的核酸进行了PCR和RT - PCR检测,以部分扩增五种病毒[牛病毒性腹泻病毒(BVDV)、牛α疱疹病毒1型(BoAHV1)、牛呼吸道合胞病毒(BRSV)、牛副流感病毒3型(BPIV - 3)和牛冠状病毒(BCoV)]以及四种与BRD病因有关的细菌[牛支原体、溶血曼氏杆菌、多杀性巴氏杆菌和睡眠嗜组织菌]的基因。来自患有BRD的动物的所有九个生物样本对BoAHV1、BRSV、BPIV - 3、BCoV和睡眠嗜组织菌检测均为阴性。因此,可以排除这些微生物参与BRD疫情的病因。在牛的下呼吸道单一和混合感染中能够鉴定出BVDV和牛支原体的存在。在两个鼻拭子中也鉴定出了BVDV:一个是单一病原体,另一个与两种细菌(多杀性巴氏杆菌和溶血曼氏杆菌)相关。对BVDV扩增子的5'UTR区域和N基因的核苷酸序列进行的系统发育分析表明,此次BRD疫情的BVDV田间毒株属于2b亚型。据我们所知,这是巴西首次报道BVDV - 2b参与BRD的病因。最后,有必要强调的是,这些牛来自一个开放式奶牛群,每半年接种一次BVDV - 1a和 - 2a疫苗。