Romey Aurore, Ularamu Hussaini G, Bulut Abdulnaci, Jamal Syed M, Khan Salman, Ishaq Muhammad, Eschbaumer Michael, Belsham Graham J, Bernelin-Cottet Cindy, Relmy Anthony, Gondard Mathilde, Benfrid Souheyla, Wungak Yiltawe S, Hamers Claude, Hudelet Pascal, Zientara Stéphan, Bakkali Kassimi Labib, Blaise-Boisseau Sandra
Animal Health Laboratory, Foot-and-Mouth Reference Laboratory, Virology JRU, ANSES, INRAE, ENVA, Paris-Est University, Maisons-Alfort 94700, France.
FMD Research Centre, National Veterinary Research Institute (NVRI), PMB 01 Vom, Lagos, Nigeria.
Transbound Emerg Dis. 2023 Aug 5;2023:9555213. doi: 10.1155/2023/9555213. eCollection 2023.
Identification and characterization of the foot-and-mouth disease virus (FMDV) strains circulating in endemic countries and their dynamics are essential elements of the global FMD control strategy. Characterization of FMDV is usually performed in reference laboratories (RL). However, shipping of FMD samples to RL is a challenge due to the cost and biosafety requirements of transportation, resulting in a lack of knowledge about the strains circulating in some endemic areas. In order to simplify this step and to encourage sample submission to RL, we have previously developed a low-cost protocol for the shipment of FMD samples based on the use of lateral flow devices (LFDs) combined with a simple virus inactivation step using 0.2% citric acid. The present study aimed to evaluate this inactivation protocol in the field. For this purpose, 60 suspected FMD clinical samples were collected in Nigeria, Pakistan, and Turkey, three countries where FMD is endemic. Sample treatment, testing on LFDs, and virus inactivation steps were performed in the field when possible. The effectiveness of the virus inactivation was confirmed at the RL. After RNA extraction from the 60 inactivated LFDs, all were confirmed as FMDV positive by real-time reverse transcription polymerase chain reaction (RT-PCR). The serotype was identified by conventional RT-PCR for 86% of the samples. The topotype and/or lineage was successfully determined for 60% of the samples by Sanger sequencing and sequence analyses. After chemical transfection of RNA extracted from inactivated LFDs, into permissive cells, infectious virus was rescued from 15% of the samples. Implementation of this user-friendly protocol can substantially reduce shipping costs, which should increase the submission of field samples and therefore improve knowledge of the circulating FMDV strains.
识别和鉴定口蹄疫病毒(FMDV)在流行国家中传播的毒株及其动态是全球口蹄疫控制策略的重要组成部分。FMDV的鉴定通常在参考实验室(RL)中进行。然而,由于运输成本和生物安全要求,将FMD样本运往RL是一项挑战,导致对一些流行地区传播的毒株缺乏了解。为了简化这一步骤并鼓励向RL提交样本,我们之前开发了一种基于使用侧向流动装置(LFD)并结合使用0.2%柠檬酸进行简单病毒灭活步骤的低成本FMD样本运输方案。本研究旨在评估该灭活方案在实际应用中的效果。为此,在尼日利亚、巴基斯坦和土耳其这三个口蹄疫流行的国家收集了60份疑似FMD临床样本。样本处理、在LFD上进行检测以及病毒灭活步骤尽可能在现场进行。病毒灭活的有效性在RL得到了证实。从60个灭活的LFD中提取RNA后,通过实时逆转录聚合酶链反应(RT-PCR)均确认为FMDV阳性。86%的样本通过常规RT-PCR鉴定了血清型。通过Sanger测序和序列分析成功确定了60%样本的拓扑型和/或谱系。将从灭活的LFD中提取的RNA化学转染到易感细胞中后,15%的样本拯救出了感染性病毒。实施这种用户友好的方案可以大幅降低运输成本,这应该会增加现场样本的提交,从而提高对口蹄疫病毒传播毒株的了解。