推进根除脊髓灰质炎病毒:从高风险和重点地区试行直接分子检测脊髓灰质炎病毒的经验教训。

IF 3.8 2区 生物学 Q2 MICROBIOLOGY
Microbiology spectrum Pub Date : 2025-02-04 Epub Date: 2024-12-12 DOI:10.1128/spectrum.02279-24
Paula L Marcet, Brandon Short, Ashley Deas, Hong Sun, Chelsea Harrington, Shahzad Shaukat, Muhammad Masroor Alam, Marycelin Baba, Adedayo Faneye, Prossy Namuwulya, Lea Necitas Apostol, Tamer Elshaarawy, John Kofi Odoom, Peter Borus, Shelina Moonsamy, Yogolelo Riziki, Marie Claire Endegue Zanga, Mesfin Tefera, Anfumbom K W Kfutwah, Salmaan Sharif, Varja Grabovac, Cara C Burns, Nancy Gerloff
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引用次数: 0

摘要

在全球脊髓灰质炎实验室网络(GPLN)中,急性弛缓性麻痹(AFP)监测的脊髓灰质炎病毒(PV)筛查结果是基于通过细胞培养分离病毒(VI),这需要较长的周转时间和活的脊髓灰质炎病毒扩增。GPLN合作伙伴已经开发并广泛验证了一种可替代的直接检测策略(DD-ITD),用于从粪便中筛选病毒核酸,而无需进行病毒培养。来自世卫组织非洲、西太平洋和东地中海区域的GPLN实验室设想了一个多实验室示范项目,对野生血清1型或疫苗衍生脊髓灰质炎病毒仍然流行的地区的DD-ITD方法进行实地测试。战略选择的实验室被要求同时使用当前的金标准VI方法和新的DD-ITD策略处理粪便悬浮液。对12个实验室的结果进行汇编和分析,以评估每次RNA提取和rRT-PCR运行的质量。对超过10,500个标本的两种方法的匹配结果显示,总体方法一致性为91%。所有实验室使用DD-ITD策略检测到的PV推定阳性样本比使用VI检测到的多,但很大一部分DD-ITD阳性结果(72%)是不确定的或无法分型的,需要通过测序来确认。两种方法共298份(2.8%)样品均为PV阳性,828份(7.9%)样品仅为DD-ITD阳性,62份(0.6%)样品仅为VI阳性。参与实验室的DD-ITD总体性能、结果质量和方法结果之间的一致性存在显著差异。DD-ITD的实施将需要建立先进分子实验室技术和数据分析的熟练程度,并增加对验证性测序的需求。重要性:急性弛缓性麻痹(AFP)监测和敏感的脊髓灰质炎病毒检测是世卫组织全球根除脊髓灰质炎战略的关键组成部分。本工作总结了一项多实验室评估的结果,该评估旨在实地测试不需要扩增脊髓灰质炎活病毒的分子直接检测策略(DD-ITD)的性能和适用性。AFP样品与DD-ITD和当前的金标准PV检测方法并行处理,基于通过细胞培养分离病毒(VI)。所有参与的实验室使用DD-ITD策略检测到的PV推定阳性样本比使用病毒分离方法检测到的多,尽管DD-ITD结果需要验证性测序的比例更高。在结果质量和总体DD-ITD性能方面,实验室之间存在显著差异。实施DD-ITD需要熟练掌握先进的分子实验室技术和加强数据分析技能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Advancing poliovirus eradication: lessons learned from piloting direct molecular detection of polioviruses in high-risk and priority geographies.

In the Global Polio Laboratory Network (GPLN), poliovirus (PV) screening results from acute flaccid paralysis (AFP) surveillance is based on virus isolation (VI) through cell culture, entailing long turnaround times and the amplification of live poliovirus. An alternative Direct Detection strategy (DD-ITD) for screening viral nucleic acid from stools, bypassing the need for virus culture, has been developed and extensively validated by GPLN partners. A multi-laboratory demonstration project was conceived to field-test the DD-ITD method by GPLN laboratories from the WHO African, Western Pacific, and Eastern Mediterranean regions, where wild serotype 1 or vaccine-derived polioviruses still circulate. Strategically selected laboratories were tasked to simultaneously process stool suspensions with the current gold-standard VI method and the new DD-ITD strategy. Results from 12 laboratories were compiled and analyzed to assess the quality of each RNA extraction and rRT-PCR run. Matched results for both methods of over 10,500 specimens showed an overall method agreement of 91%. All laboratories detected more PV presumptive positive samples with the DD-ITD strategy than with VI, but a large proportion of DD-ITD positive results (72%) were inconclusive or non-typeable, requiring confirmation through sequencing. A total of 298 (2.8%) samples were PV positive using both methods, 828 (7.9%) positive only for DD-ITD, and 62 (0.6%) positive only with VI. The DD-ITD overall performance, quality of results, and agreement between method results varied significantly across participating laboratories. DD-ITD implementation would entail building proficiency in advanced molecular laboratory techniques and data analysis, and increased demand for confirmatory sequencing.

Importance: Surveillance of acute flaccid paralysis (AFP) and sensitive poliovirus detection are key components of the WHO Global Polio Eradication Strategy. This work summarizes the results of a multi-laboratory evaluation designed to field-test the performance and applicability of a molecular Direct Detection strategy (DD-ITD) that does not require amplification of live poliovirus. AFP samples were processed in parallel with both the DD-ITD and the current gold-standard PV detection methodology, based on virus isolation (VI) through cell culture. All participating laboratories detected more PV presumptive positive samples using the DD-ITD strategy than with virus isolation methodology, although a higher proportion of DD-ITD results required confirmatory sequencing. Significant variability among laboratories was observed in the quality of the results and overall DD-ITD performance. Implementing DD-ITD would entail building proficiency in advanced molecular laboratory techniques and strengthening data analysis skills.

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来源期刊
Microbiology spectrum
Microbiology spectrum Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.20
自引率
5.40%
发文量
1800
期刊介绍: Microbiology Spectrum publishes commissioned review articles on topics in microbiology representing ten content areas: Archaea; Food Microbiology; Bacterial Genetics, Cell Biology, and Physiology; Clinical Microbiology; Environmental Microbiology and Ecology; Eukaryotic Microbes; Genomics, Computational, and Synthetic Microbiology; Immunology; Pathogenesis; and Virology. Reviews are interrelated, with each review linking to other related content. A large board of Microbiology Spectrum editors aids in the development of topics for potential reviews and in the identification of an editor, or editors, who shepherd each collection.
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