Frucchi Ana Paula S, Dall Agnol Alais M, Bronkhorst Dalton E, Beuttemmuller Edsel A, Alfieri Amauri A, Alfieri Alice F
Laboratory of Animal Virology, Department of Veterinary Preventive Medicine, Universidade Estadual de Londrina, Londrina, Brazil.
Multi-User Animal Health Laboratory, Molecular Biology Unit, Department of Veterinary Preventive Medicine, Universidade Estadual de Londrina, Londrina, Brazil.
Front Vet Sci. 2022 May 25;9:895492. doi: 10.3389/fvets.2022.895492. eCollection 2022.
Bovine respiratory disease (BRD) is considered a major cause of morbidity and mortality in young calves and is caused by a range of infectious agents, including viruses and bacteria. This study aimed to determine the frequency of viral and bacterial pathogens detected in calves with BRD from high-production dairy cattle herds and to perform the molecular characterization of N and S1 genes in identified bovine coronavirus (BCoV) strains. Nasal swabs were collected from 166 heifer calves, namely, 85 symptomatic and 81 asymptomatic calves aged between 5 and 90 days, from 10 dairy cattle herds. Nasal swabs were evaluated using molecular techniques for the identification of viruses (BCoV, bovine alphaherpesvirus 1, bovine viral diarrhea virus, bovine parainfluenza virus 3, and bovine respiratory syncytial virus) and bacteria (, and ). In addition, five and two BCoV-positive samples were submitted to N and S1 gene amplification and nucleotide sequencing, respectively. The frequency of diagnosis of BCoV was higher (56%, 93/166) than the frequency of (39.8%, 66/166) and (33.1%, 55/166). The three microorganisms were identified in the calves of symptomatic and asymptomatic heifer calve groups. All other pathogens included in the analyses were negative. In the phylogenetic analysis of the S1 gene, the Brazilian strains formed a new branch, suggesting a new genotype, called # 15; from the N gene, the strains identified here belonged to cluster II. This study describes high rates of BCoV, , and in heifer calves from high-production dairy cattle herds with BRD. Additionally, the molecular characterization provides evidence that the circulating BCoV strains are ancestrally different from the prototype vaccine strains and even different BCoV strains previously described in Brazil.
牛呼吸道疾病(BRD)被认为是幼龄犊牛发病和死亡的主要原因,它由多种传染因子引起,包括病毒和细菌。本研究旨在确定高产奶牛群中患BRD的犊牛体内检测到的病毒和细菌病原体的频率,并对鉴定出的牛冠状病毒(BCoV)毒株的N基因和S1基因进行分子特征分析。从10个奶牛群中采集了166头小母牛犊牛的鼻拭子,其中85头有症状,81头无症状,年龄在5至90天之间。使用分子技术对鼻拭子进行评估,以鉴定病毒(BCoV、牛α疱疹病毒1型、牛病毒性腹泻病毒、牛副流感病毒3型和牛呼吸道合胞病毒)和细菌(此处原文缺失细菌名称)。此外,分别对5个和2个BCoV阳性样本进行了N基因和S1基因扩增及核苷酸测序。BCoV的诊断频率(56%,93/166)高于此处原文缺失细菌名称(39.8%,66/166)和此处原文缺失细菌名称(33.1%,55/166)的频率。在有症状和无症状小母牛犊牛组的犊牛中均鉴定出这三种微生物。分析中包括的所有其他病原体均为阴性。在S1基因的系统发育分析中,巴西毒株形成了一个新分支,表明存在一种新的基因型,称为#15;从N基因来看,此处鉴定出的毒株属于第二簇。本研究描述了高产奶牛群中患BRD的小母牛犊牛体内BCoV、此处原文缺失细菌名称和此处原文缺失细菌名称的高感染率。此外,分子特征分析提供了证据,表明流行的BCoV毒株在谱系上不同于原型疫苗毒株,甚至与巴西先前描述的不同BCoV毒株也不同。