Lemaitre Evelyne, Bougeard Stéphanie, Allée Chantal, Eterradossi Nicolas, Courtillon Céline, Brown Paul Alun
Ploufragan-Plouzané-Niort Laboratory, French Agency for Food, Environmental and Occupational Health & Safety (Anses), VIPAC Unit, WOAH Reference Laboratory for Avian Metapneumovirus Infections, Ploufragan, France.
Ploufragan-Plouzané-Niort Laboratory, French Agency for Food, Environmental and Occupational Health & Safety (Anses), EPISABE Unit, Ploufragan, France.
Front Vet Sci. 2022 Nov 15;9:1058294. doi: 10.3389/fvets.2022.1058294. eCollection 2022.
End-point and real-time avian metapneumovirus (AMPV) RT-PCRs have been developed to detect one or two of the four recognized subgroups (A,B,C, and D) simultaneously or for broad range AMPV detection. Current subgroup specific tests target variable areas of the genome which makes these PCRs sensitive to specificity defects as recently documented. In the current study, a single five-plex digital droplet RT-PCR targeting the conserved viral polymerase gene of AMPV, which is less prone to genetic drift, has been designed. This digital droplet RT-PCR was capable of identifying each of the four AMPV subgroups. Each subgroup was identified according to a specifically assigned fluorescent amplitude. Specificity, which was tested including 31 AMPV strains, non-AMPV avian viruses and closely related human respiratory viruses, was 100%. The specific limit of detection for extracted viral RNA was estimated between 1 and 3 copies/μl. This tool simplifies the number of tests required for AMPV genotype diagnostics and should be theoretically less effected by viral genome evolution due to its target region. Ultimately, application of this test will contribute to an improved understanding of the global geographic distribution and subgroup host range of field strains.
已开发出终点和实时禽偏肺病毒(AMPV)逆转录聚合酶链反应(RT-PCR),用于同时检测四种公认亚组(A、B、C和D)中的一种或两种,或用于广泛检测AMPV。目前的亚组特异性检测针对基因组的可变区域,这使得这些PCR对最近记录的特异性缺陷敏感。在本研究中,设计了一种针对AMPV保守病毒聚合酶基因的单重五重数字液滴RT-PCR,该基因不易发生基因漂移。这种数字液滴RT-PCR能够识别四种AMPV亚组中的每一种。根据特定分配的荧光幅度识别每个亚组。包括31株AMPV毒株、非AMPV禽病毒和密切相关的人类呼吸道病毒在内的特异性测试显示,特异性为100%。提取的病毒RNA的特异性检测限估计在1至3拷贝/微升之间。该工具简化了AMPV基因型诊断所需的检测数量,并且由于其靶区域,理论上应受病毒基因组进化的影响较小。最终,该检测方法的应用将有助于更好地了解田间毒株的全球地理分布和亚组宿主范围。