Department of Disease Control, London School of Hygiene & Tropical Medicine, London, United Kingdom.
Rajendra Memorial Research Institute of Medical Sciences, Patna, India.
PLoS Negl Trop Dis. 2023 Sep 1;17(9):e0011200. doi: 10.1371/journal.pntd.0011200. eCollection 2023 Sep.
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 12x12 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. No significant differences in Leishmania RNA detection and quantitation between methods were observed in experimentally infected sand flies maintained in conditions simulating field conditions. 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.
在整个印度次大陆,黑热病消除计划已经导致内脏利什曼病(VL)病例显著减少。为了检测任何传播的复发,需要一个敏感且具有成本效益的监测系统。分子 Xenomonitoring(MX),即检测媒介中的病原体 DNA/RNA,为淋巴丝虫病消除计划中的人类感染提供了一个替代指标。为了确定 MX 是否可用于低传播环境中的 VL 监测,需要大量的沙蝇媒介白蛉属 argentipes。本研究将确定捕获白蛉属 argentipes 雌性的最佳方法,以便进行 MX。
方法/主要发现:该现场研究在印度比哈尔邦的两个规划和两个非规划村庄进行。共招募了 48 户家庭(每村 12 户)。使用标准方法比较了疾病控制和预防中心的光阱(CDC-LTs)与改良 Prokopack(PKP)和机械真空抽吸器(MVA)。尝试了四个 12x12 的拉丁方,共进行了 576 次采集(每户 12 次,每个村庄 144 次,每个方法 192 次)。对采集物进行分子分析,以确认白蛉属 argentipes 的鉴定,并检测人类和利什曼原虫 DNA。还考虑了操作因素,如时间负担、房主接受程度和 RNA 保存。共完成了 562 次采集(97.7%),共捕获了 6809 只沙蝇。雌性占捕获量的 49.0%,其中 1934 只(57.9%)被鉴定为白蛉属 argentipes。CDC-LTs 比 MVA 多收集了 4.04 倍的白蛉属 argentipes 雌性,比 PKP 多收集了 3.62 倍(每种方法均<0.0001)。在相同的采集物中,有 21735 只蚊子,没有观察到采集方法之间的显著差异。CDC-LTs 的安装和采集时间比抽吸时间短,但其更高的产量弥补了增加的分类时间。在模拟野外条件下饲养的实验感染白蛉属 argentipes 中,没有观察到方法之间利什曼原虫 RNA 检测和定量的显著差异。房主更喜欢使用 CDC-LTs。
结论/意义:在 MX 监测中,CDC-LTs 是最有用的采集工具,因为它们收集了更多的白蛉属 argentipes 雌性,而不会影响蚊子的捕获或 RNA 的保存。然而,捕获率仍然很低。