Gigante Crystal M, Hartloge Claire, Condori Rene Edgar, Kirby Jordona D, Hovis Lauren, Nelson Kathleen M, Wallace Ryan, Li Yu, Chipman Richard B
Poxvirus and Rabies Branch, Division of High-Consequence Pathogens and Pathology, United States of America Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.
USDA, APHIS, Wildlife Services, National Rabies Management Program, Concord, New Hampshire, United States of America.
PLoS Negl Trop Dis. 2025 Jul 18;19(7):e0013348. doi: 10.1371/journal.pntd.0013348. eCollection 2025 Jul.
Roadkill specimens are an important source of samples for enhanced rabies surveillance (ERS) in areas where other methods of sample collection may not be practical. However, the physical condition of roadkill specimens is unpredictable and, in many circumstances, unsatisfactory for rabies diagnostic testing by antigen detection methods. The high sensitivity of real-time reverse transcriptase PCR (RT-PCR) holds promise for rabies diagnostic testing of poor-quality samples. We conducted an evaluation of real-time RT-PCR to detect rabies virus RNA in roadkill samples. A total of 299 specimens were collected from raccoons (n = 232), skunks (n = 46), foxes (n = 17), coyotes (n = 2), a bobcat (n = 1), and a domestic cat (n = 1) across ten states during 2018 - 2021 in the United States. Eight samples (2.7%) were positive using the LN34 pan-lyssavirus real-time RT-PCR assay. These eight rabid animals in areas of high interest for wildlife rabies management would likely not have been identified otherwise. These findings support the use of real-time RT-PCR for samples that would typically be unsuitable for testing by widely used antigenic-based detection methods such as the direct fluorescent antibody test (DFA or FAT) and direct rapid immunohistochemistry test (DRIT).
在一些其他样本采集方法可能不实用的地区,公路死亡动物标本是加强狂犬病监测(ERS)的重要样本来源。然而,公路死亡动物标本的身体状况不可预测,而且在许多情况下,其状况不适合用抗原检测方法进行狂犬病诊断测试。实时逆转录酶PCR(RT-PCR)的高灵敏度为劣质样本的狂犬病诊断测试带来了希望。我们对实时RT-PCR检测公路死亡动物样本中狂犬病病毒RNA进行了评估。2018年至2021年期间,在美国十个州共采集了299个标本,其中浣熊(n = 232)、臭鼬(n = 46)、狐狸(n = 17)、郊狼(n = 2)、一只山猫(n = 1)和一只家猫(n = 1)。使用LN34全狂犬病病毒属实时RT-PCR检测法,有八个样本(2.7%)呈阳性。否则,野生动物狂犬病管理重点关注地区的这八只狂犬病动物可能无法被识别出来。这些发现支持对通常不适用于通过广泛使用的基于抗原的检测方法(如直接荧光抗体检测(DFA或FAT)和直接快速免疫组织化学检测(DRIT))进行检测的样本使用实时RT-PCR。