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用于检测居住在莱姆病流行地区的美国患者中波瓦桑病毒感染的血清学检测组合的开发与验证

Development and Validation of a Serologic Test Panel for Detection of Powassan Virus Infection in U.S. Patients Residing in Regions Where Lyme Disease Is Endemic.

作者信息

Thomm Angela M, Schotthoefer Anna M, Dupuis Alan P, Kramer Laura D, Frost Holly M, Fritsche Thomas R, Harrington Yvette A, Knox Konstance K, Kehl Sue C

机构信息

Coppe Laboratories, Waukesha, Wisconsin, USA.

Marshfield Clinic Research Foundation, Marshfield, Wisconsin, USA.

出版信息

mSphere. 2018 Jan 10;3(1). doi: 10.1128/mSphere.00467-17. eCollection 2018 Jan-Feb.

DOI:10.1128/mSphere.00467-17
PMID:29359181
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5760746/
Abstract

Powassan virus (POWV) is an emerging tick-borne arbovirus presenting a public health threat in North America. POWV lineage II, also known as deer tick virus, is the strain of the virus most frequently found in ticks and is implicated in most cases of POWV encephalitis in the United States. Currently, no commercial tests are available to detect POWV exposure in tick-borne disease (TBD) patients. We describe here the development and analytical validation of a serologic test panel to detect POWV infections. The panel uses an indirect enzyme immunoassay (EIA) to screen. EIA-positive samples reflex to a laboratory-developed, POWV-specific immunofluorescence assay (IFA). The analytical sensitivity of the test panel was 89%, and the limit of detection was a plaque reduction neutralization test (PRNT) titer of 1:20. The analytical specificity was 100% for the IgM assay and 65% for the IgG assay when heterologous-flavivirus-positive samples were tested. On samples collected from regions where Lyme disease is endemic, seroprevalence for POWV in TBD samples was 9.4% (10 of 106) versus 2% when tested with non-TBD samples (2 of 100, = 0.034). No evidence of POWV infection was seen in samples collected from a region where Lyme disease was not endemic (0 of 22). This test panel provides a sensitive and specific platform for detecting a serologic response to POWV early in the course of infection when neutralizing antibodies may not be detectable. Combined with clinical history, the panel is an effective tool for identifying acute POWV infection. Approximately 100 cases of POWV disease were reported in the United States over the past 10 years. Most cases have occurred in the Northeast (52) and Great Lakes (45) regions (https://www.cdc.gov/powassan/statistics.html). The prevalence of POWV in ticks and mammals is increasing, and POWV poses an increasing threat in a greater geographical range. In areas of the Northeast and Midwest where Lyme disease is endemic, POWV testing is recommended for patients with a recent tick bite, patients with Lyme disease who have been treated with antibiotics, or patients with a tick exposure who have tested negative for Lyme disease or other tick-borne illnesses and have persistent symptoms consistent with posttreatment Lyme disease. Testing could also benefit patients with tick exposure and unexplained neurologic symptoms and chronic fatigue syndrome (CFS) patients with known tick exposure. Until now, diagnostic testing for Powassan virus has not been commercially available and has been limited to patients presenting with severe, neurologic complications. The lack of routine testing for Powassan virus in patients with suspected tick-borne disease means that little information is available regarding the overall prevalence of the virus and the full spectrum of clinical symptoms associated with infection. As is the tick vector for Powassan virus and multiple other tick-borne pathogens, including the Lyme disease bacterium, , the clinical presentations and long-term outcomes of Powassan virus infection and concurrent infection with other tick-borne disease pathogens remain unknown.

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7ea/5760746/ad994393de26/sph0011824510002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7ea/5760746/7f49641f18ba/sph0011824510001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7ea/5760746/ad994393de26/sph0011824510002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7ea/5760746/7f49641f18ba/sph0011824510001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7ea/5760746/ad994393de26/sph0011824510002.jpg
摘要

波瓦桑病毒(POWV)是一种新出现的蜱传虫媒病毒,对北美的公共卫生构成威胁。POWV II系,也称为鹿蜱病毒,是在蜱虫中最常发现的病毒株,与美国大多数POWV脑炎病例有关。目前,尚无商业检测方法可用于检测蜱传疾病(TBD)患者是否感染POWV。我们在此描述了一种用于检测POWV感染的血清学检测方法的开发和分析验证。该检测方法采用间接酶免疫测定(EIA)进行筛查。EIA阳性样本会转至实验室开发的POWV特异性免疫荧光测定(IFA)进行检测。该检测方法的分析灵敏度为89%,检测限为蚀斑减少中和试验(PRNT)滴度1:20。在检测异源黄病毒阳性样本时,IgM检测的分析特异性为100%,IgG检测的分析特异性为65%。在莱姆病流行地区采集的样本中,TBD样本中POWV的血清阳性率为9.4%(106例中的10例),而非TBD样本的血清阳性率为2%(100例中的2例,P = 0.034)。在莱姆病非流行地区采集的样本中未发现POWV感染迹象(22例中的0例)。该检测方法提供了一个敏感且特异的平台,可在感染早期中和抗体可能无法检测到时,检测对POWV的血清学反应。结合临床病史,该检测方法是识别急性POWV感染的有效工具。在过去10年中,美国报告了约100例POWV疾病病例。大多数病例发生在东北部(52例)和五大湖地区(45例)(https://www.cdc.gov/powassan/statistics.html)。POWV在蜱虫和哺乳动物中的流行率正在上升,并且POWV在更大的地理范围内构成的威胁也在增加。在东北部和中西部莱姆病流行的地区,建议对近期被蜱叮咬的患者、接受过抗生素治疗的莱姆病患者,或有蜱虫接触史且莱姆病或其他蜱传疾病检测呈阴性但有与莱姆病治疗后持续症状相符的持续性症状的患者进行POWV检测。检测也可能使有蜱虫接触史且有无法解释的神经症状的患者以及已知有蜱虫接触史的慢性疲劳综合征(CFS)患者受益。到目前为止,针对波瓦桑病毒的诊断检测尚无商业可用方法,并且仅限于出现严重神经并发症的患者。对疑似蜱传疾病患者缺乏波瓦桑病毒的常规检测意味着关于该病毒的总体流行率以及与感染相关的全部临床症状信息很少。由于蜱是波瓦桑病毒和多种其他蜱传病原体(包括莱姆病细菌)的传播媒介,波瓦桑病毒感染以及与其他蜱传疾病病原体并发感染的临床表现和长期后果仍然未知。

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