Simultaneous detection of canine astrovirus and canine kobuvirus by duplex qPCR: validation and evidence of extraintestinal viral RNA in naturally infected dogs.

IF 1.1 3区 农林科学 Q3 VETERINARY SCIENCES
Tin Van Nguyen, Tanit Kasantikul, Chutchai Piewbang, Somporn Techangamsuwan
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引用次数: 0

Abstract

Canine astrovirus (mamastrovirus 5 [MAstV5], formerly CaAstV; family Astroviridae, taxon species Mamastrovirus canis) and canine kobuvirus (aichivirus A2 [AiV-A2], formerly CaKoV; Picornaviridae, Kobuvirus aichi) are emerging enteric viruses increasingly detected in both diarrheic and subclinical dogs. Although primarily associated with gastrointestinal illness, recent evidence suggests a potential for systemic dissemination, which remains insufficiently explored. To improve detection, we developed and validated a duplex quantitative real-time PCR (dqPCR) assay for simultaneous identification of MAstV5 and AiV-A2. Primers and TaqMan probes were designed based on conserved regions of the MAstV5 ORF1b and AiV-A2 3D polymerase genes. Assay optimization included primer-probe concentration titration and thermal gradient analysis. Analytical performance was assessed using synthetic plasmid standards and RNA from non-target viruses, including canine parvovirus (CPV), canine morbillivirus (CDV), and canine enteric coronavirus (CCoV). Our dqPCR assay had high linearity (R2 > 0.99) and sensitivity, with limits of detection of 10 copies/μL for MAstV5 and 100 copies/μL for AiV-A2. No cross-reactivity or interference was observed in coinfection simulations across various target ratios. Intra- and inter-assay CV values were <2.2%, indicating excellent reproducibility. Validation using 50 clinical rectal swabs and tissue samples from 25 autopsied dogs revealed 1 additional AiV-A2-positive case undetected by RT-PCR but confirmed by sequencing. Importantly, viral RNA was also found in extraintestinal tissues-spleen, liver, trachea, and mesenteric lymph nodes-suggesting systemic distribution in naturally infected dogs. Our dqPCR assay provides a sensitive, specific, and efficient tool for the detection of MAstV5 and AiV-A2, supporting both clinical testing and epidemiologic studies.

双工qPCR同时检测犬星状病毒和犬科布病毒:自然感染犬肠外病毒RNA的验证和证据。
犬星状病毒(乳突病毒5 [MAstV5],原CaAstV;星状病毒科,分类种犬乳突病毒)和犬柯布病毒(柯布病毒A2 [AiV-A2],原CaKoV;小鸟状病毒科,柯布病毒爱知)是新兴的肠道病毒,在腹泻和亚临床犬中越来越多地发现。虽然主要与胃肠道疾病有关,但最近的证据表明,它可能会在全身传播,但这方面的探索还不够充分。为了提高检测水平,我们开发并验证了一种双工实时定量PCR (dqPCR)方法,用于同时鉴定MAstV5和AiV-A2。引物和TaqMan探针基于MAstV5 ORF1b和AiV-A2 3D聚合酶基因的保守区域设计。实验优化包括引物-探针浓度滴定和热梯度分析。采用合成质粒标准品和非靶病毒(包括犬细小病毒(CPV)、犬麻疹病毒(CDV)和犬肠道冠状病毒(CCoV))的RNA来评估分析性能。dqPCR检测方法线性度高(R2 > 0.99),灵敏度高,MAstV5的检测限为10 copies/μL, AiV-A2的检测限为100 copies/μL。在不同靶比的共感染模拟中未观察到交叉反应或干扰。试验内和试验间CV值分别为
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来源期刊
CiteScore
3.00
自引率
6.70%
发文量
127
审稿时长
6-16 weeks
期刊介绍: The Journal of Veterinary Diagnostic Investigation (J Vet Diagn Invest) is an international peer-reviewed journal published bimonthly in English by the American Association of Veterinary Laboratory Diagnosticians (AAVLD). JVDI is devoted to all aspects of veterinary laboratory diagnostic science including the major disciplines of anatomic pathology, bacteriology/mycology, clinical pathology, epidemiology, immunology, laboratory information management, molecular biology, parasitology, public health, toxicology, and virology.
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