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一种用于检测犊牛腹泻病毒的多重实时荧光定量PCR检测方法。

A multiplex real-time fluorescence-based quantitative PCR assay for calf diarrhea viruses.

作者信息

Meng Wenxin, Chen Zihan, Jiang Qifeng, Chen Jinping, Guo Xiaoying, Ma Zihang, Jia Kun, Li Shoujun

机构信息

College of Veterinary Medicine, South China Agricultural University, Guangzhou, China.

Guangdong Technological Engineering Research Center for Pet, Guangzhou, China.

出版信息

Front Microbiol. 2024 Jan 5;14:1327291. doi: 10.3389/fmicb.2023.1327291. eCollection 2023.

Abstract

INTRODUCTION

Calf diarrhea is a significant condition that has a strong effect on the cattle industry, resulting in huge economic losses annually. Bovine torovirus (BToV), bovine enterovirus (BEV), bovine norovirus (BNoV), bovine coronavirus (BCoV), bovine rotavirus (BRV), and bovine viral diarrhea virus (BVDV) are key pathogens that have been implicated in calf diarrhea. Among these viruses, there remains limited research on BToV, BEV, and BNoV, with no available vaccines or drugs for their prevention and control. Although commercial vaccines exist for BCoV, BRV, and BVDV, the prevalence of these diseases remains high.

METHODS

To address this issue, we developed a multiplex real-time fluorescence quantitative PCR method for detecting BToV, BEV, BNoV, BCoV, BRV, and BVDV. This method can be used to effectively monitor the prevalence of these six viruses and serve as a reference for future prevention and control strategies. In this study, we specifically designed primers and probes for the BNoV Rdrp, BEV 5'UTR, BToV M, BCoV N, BRV NSP5, and BVDV 5'UTR genes.

RESULTS

This method was determined to be efficient, stable, and sensitive. The lowest detectable levels of plasmids for BNoV, BEV, BToV, BRV, BCoV, and BVDV were 1.91 copies/μL, 96.0 copies/μL, 12.8 copies/μL, 16.4 copies/μL, 18.2 copies/μL, and 65.3 copies/μL, respectively. Moreover, the coefficients of variation for all six detection methods were < 3%; they also exhibited a strong linear relationship (R ≥ 0.98), and an amplification efficiency of 90%-110%. A total of 295 fecal and anal swabs were collected from calves with diarrhea in Guangdong, China. The positive rates for BToV, BEV, BNoV, BCoV, BR, and BVDV were determined to be 0.34% (1/295), 6.10% (18/295), 0.68% (2/295), 1.36% (4/295), 10.85% (32/295), and 2.03% (6/295), respectively. Notably, BEV and BRV exhibited the highest prevalence.

DISCUSSION

Additionally, this study identified the occurrence of BToV and BNoV in Guangdong for the first time. In summary, this study successfully established an effective method for detecting several important bovine viruses; ultimately, this holds strong implications for the future development of the cattle industry.

摘要

引言

犊牛腹泻是一种对养牛业有重大影响的疾病,每年造成巨大经济损失。牛环曲病毒(BToV)、牛肠道病毒(BEV)、牛诺如病毒(BNoV)、牛冠状病毒(BCoV)、牛轮状病毒(BRV)和牛病毒性腹泻病毒(BVDV)是与犊牛腹泻有关的主要病原体。在这些病毒中,对BToV、BEV和BNoV的研究仍然有限,尚无用于预防和控制它们的疫苗或药物。尽管有针对BCoV、BRV和BVDV的商业疫苗,但这些疾病的流行率仍然很高。

方法

为解决这一问题,我们开发了一种用于检测BToV、BEV、BNoV、BCoV、BRV和BVDV的多重实时荧光定量PCR方法。该方法可用于有效监测这六种病毒的流行情况,并为未来的预防和控制策略提供参考。在本研究中,我们专门为BNoV RdRp、BEV 5'UTR、BToV M、BCoV N、BRV NSP5和BVDV 5'UTR基因设计了引物和探针。

结果

该方法被确定为高效、稳定且灵敏。BNoV、BEV、BToV、BRV、BCoV和BVDV质粒的最低检测水平分别为1.91拷贝/μL、96.0拷贝/μL、12.8拷贝/μL、16.4拷贝/μL、18.2拷贝/μL和65.3拷贝/μL。此外,所有六种检测方法的变异系数均<3%;它们还表现出很强的线性关系(R≥0.98),扩增效率为90%-110%。从中国广东腹泻犊牛中总共采集了295份粪便和肛门拭子。确定BToV、BEV、BNoV、BCoV、BR和BVDV的阳性率分别为0.34%(1/295)、6.10%(18/295)、0.68%(2/295)、1.36%(4/295)、10.85%(32/295)和2.03%(6/295)。值得注意的是,BEV和BRV的流行率最高。

讨论

此外,本研究首次在广东发现了BToV和BNoV的存在。总之,本研究成功建立了一种检测几种重要牛病毒的有效方法;最终,这对养牛业的未来发展具有重要意义。

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