阿根廷白蛉和蝇类在内脏利什曼病分子监测系统中采集方法的比较

Shannon McIntyre-Nolan, Vijay Kumar, Miguella Mark Carew, Kundan Kumar, Emily Nightingale, Giorgia Dalla Libera Marchiori, Matthew Rogers, Mojca Kristan, Susana Campino, Graham F. Medley, Pradeep Das, Mary Cameron
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引用次数: 0

摘要

背景黑热病消除规划导致整个印度次大陆内脏利什曼病(VL)病例显著减少。为了发现任何重新出现的传播,需要一个敏感的、具有成本效益的监测系统。分子异种监测(MX),检测媒介中的病原体DNA/RNA,在淋巴丝虫病消除规划中提供了人类感染的代理。为了确定MX是否可以在低传播环境中用于VL监测,需要大量沙蝇媒介白蛉。本研究将确定为MX捕获阿根廷种雌虫的最佳方法。实地研究在印度比哈尔邦的两个规划村和两个非规划村进行。共招募了48户(12户/村)。采用标准化方法对美国疾病控制与预防中心的光诱器(cdc - lt)与改良Prokopack (PKP)和机械真空吸引器(MVA)进行比较。4个12×12拉丁方格共576个集合(12个/house, 144个/village,192个/method)。对收集的标本进行分子分析,以确认阿根廷假疟原虫的鉴定,并检测人类和利什曼原虫的DNA。还考虑了操作因素,如时间负担、住户接受程度和RNA保存。共完成采集562次(97.7%),捕获沙蝇6809只。雌虫占捕获总数的49.0%,其中鉴定为阿根廷种的1934只(57.9%)。cdc - lt比MVA多采集了4.04倍的阿根廷种雌虫,比PKP多采集了3.62倍(p = 0.0001)。在同一采集点的21735只蚊虫中,不同采集方法间无显著差异。cdc - lt的安装和收集时间比期望的要短,其更高的产量弥补了分选时间的增加。cdc - lt受到住户的青睐。cdc - lt是MX监测中最有用的收集工具,因为它们在不影响蚊子捕获或RNA保存的情况下收集了大量的雌性银种疟原虫。然而,捕获率仍然很低。分子异种监测是一种筛选昆虫病原DNA/RNA的方法,可用于昆虫传播疾病的监测。由于在消除疾病的目标地区,感染病原体的昆虫比例非常低,因此需要对大量雌性昆虫进行筛选。我们比较了采集印度次大陆内脏利什曼病寄生虫载体阿根廷白蛉沙蝇雌虫的三种不同方法,以确定哪种方法采集的雌虫数量最多。还考虑了其他可能影响疾病控制方案选择特定收集方法的因素,例如收集和分类样品所需的时间、户主对特定收集方法的接受程度以及昆虫样品中的RNA降解是否因收集方法而异。美国疾病控制和预防中心(cdc - lt)证明,在收集更多雌性沙蝇和保留RNA的情况下,光阱比两种吸吸方法更有用。此外,它们安装所需的时间比实现愿望所需的时间要少,因此受到户主的青睐。因此,cdc - lc被认为是最适合印度沙蝇分子异种监测的采集方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparison of collection methods forPhlebotomus argentipessand flies to use in a molecular xenomonitoring system for the surveillance of visceral leishmaniasis
Abstract Background The kala-azar elimination programme has resulted in a significant reduction in visceral leishmaniasis (VL) cases across the Indian Subcontinent. To detect any resurgence of transmission, a sensitive cost-effective surveillance system is required. Molecular xenomonitoring (MX), detection of pathogen DNA/RNA in vectors, provides a proxy of human infection in the lymphatic filariasis elimination programme. To determine whether MX can be used for VL surveillance in a low transmission setting, large numbers of the sand fly vector Phlebotomus argentipes are required. This study will determine the best method for capturing P. argentipes females for MX. Methodology/Principal Findings The field study was performed in two programmatic and two non-programmatic villages in Bihar, India. A total of 48 households (12/village) were recruited. Centers for Disease Control and Prevention light traps (CDC-LTs) were compared with Improved Prokopack (PKP) and mechanical vacuum aspirators (MVA) using standardised methods. Four 12×12 Latin squares, 576 collections, were attempted (12/house, 144/village,192/method). Molecular analyses of collections were conducted to confirm identification of P. argentipes and to detect human and Leishmania DNA. Operational factors, such as time burden, acceptance to householders and RNA preservation, were also considered. A total of 562 collections (97.7%) were completed with 6,809 sand flies captured. Females comprised 49.0% of captures, of which 1,934 (57.9%) were identified as P. argentipes . CDC-LTs collected 4.04 times more P. argentipes females than MVA and 3.62 times more than PKP (p<0.0001 for each). Of 21,735 mosquitoes in the same collections, no significant differences between collection methods were observed. CDC-LTs took less time to install and collect than to perform aspirations and their greater yield compensated for increased sorting time. CDC-LTs were favoured by householders. Conclusions/Significance CDC-LTs are the most useful collection tool of those tested for MX surveillance since they collected higher numbers of P. argentipes females without compromising mosquito captures or the preservation of RNA. However, capture rates are still low. Author Summary Molecular xenomonitoring, screening insects for pathogen DNA/RNA, may be used for surveillance of diseases transmitted by insects. Since the proportion of insects infected with pathogens is very low in areas targeted for disease elimination, large numbers of females need to be screened. We compared three different methods for collecting Phlebotomus argentipes sand fly females, the vector of parasites causing the disease visceral leishmaniasis in the Indian subcontinent, to determine which collected the largest number of females. Other factors that may also influence selection of a particular method of collection by a disease control programme, such as the time it takes to collect and sort samples, the acceptance of householders for a particular collection method and whether RNA degradation in insect samples differed between collection methods, were also considered. Centers for Disease Control and Prevention light traps (CDC-LTs) proved to be more useful than two types of aspiration methods for collecting higher numbers of sand fly females and RNA preservation was retained. Furthermore, they took less time to install than to perform aspirations and were favoured by householders. Therefore, CDC-LTs were considered to be the most suitable collection method for molecular xenomonitoring of sand flies in India.
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