在没有污水网络基础设施的环境中对土壤传播蠕虫和其他肠道病原体进行环境监测

Joel Edoux Eric Siko, Kendra Joy Dahmer, Zayina Zondervenni Manoharan, Ajithkumar Muthukumar, Heather K Amato, Christopher LeBoa, Michael Harris, Venkateshprabhu Janagaraj, Malathi Manuel, Tintu Varghese, Parfait Houngbegnon, Nils Pilotte, Bernadin Bouko, Souad Saidou, Adrian J.F. Luty, Rohan Michael Ramesh, Moudachirou Ibikounle, Sitara S.R. Ajjampur, Amy J Pickering
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摘要

土壤传播蠕虫(STH)是全球最常见的肠道传染病之一。为了控制与 STH 相关的发病率,世界卫生组织建议进行有针对性的驱虫,并改善水、环境卫生和个人卫生。目前的性传播疾病监测策略侧重于通过显微镜鉴定和量化粪便样本中的虫卵,但这种方法的特异性和敏感性较差,尤其是在感染强度较低的环境中。废水流行病学是一种用于监测病原体循环的监测工具,可以取代粪便检测 STH 的方法。然而,针对大型城市居住区以外缺乏网络化卫生设施的环境的采样策略并不完善。在此,我们报告了对没有网络卫生设施的农村和城郊地区土壤和废水性传播疾病监测采样策略的评估。我们使用多平行 qPCR 检测法检测了贝宁科姆、印度泰米尔纳德邦 Timiri 和 Jawadhu 山从人流量大的地方采集的土壤和三种废水样本(被动摩尔拭子、抓取样本和排水沟沉积物)中的 STH DNA。我们在土壤(印度 = 32/95,贝宁 = 39/121)和废水(印度 = 24/60,贝宁 = 8/64)中检测到了 STH,在所有样本类型中,印度的检测频率为 36%,贝宁为 25%。我们评估了哪些采样地点和采样类型可以更灵敏地检测到 STH DNA,并确定 STH 感染率因采样地点而异,但在特定采样地点(例如,从一个市场的多个地点采集的样本)内并无显著差异。此外,我们还确定废水沉积物样本的 STH 检测结果优于抓取样本和摩尔拭子样本。最后,我们对方法进行了扩展,包括使用多重 qPCR 对废水样本进行其他肠道病原体的检测。我们的研究结果为在没有网络卫生设施的环境中监测各种肠道病原体的环境和废水建立了采样策略。
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Environmental surveillance of soil-transmitted helminths and other enteric pathogens in settings without networked wastewater infrastructure
Soil-transmitted helminths (STH) are one of the most prevalent enteric infections world-wide. To control STH-related morbidity, the World Health Organization recommends targeted deworming and improvements in water, sanitation and hygiene. Current surveillance strategies for STH focus on identifying and quantifying eggs in stool samples via microscopy, which exhibits poor specificity and sensitivity, especially in settings with low-intensity infections. Wastewater-based epidemiology is a surveillance tool used to monitor pathogen circulation and could replace stool-based approaches for STH detection. However, sampling strategies for settings lacking networked sanitation outside large urban settlements are not well developed. Here, we report evaluation of sampling strategies for soil and wastewater STH surveillance in rural and peri-urban settings without networked sanitation. We used multi-parallel qPCR assays to detect STH DNA in soil collected from high foot-traffic locations and three types of wastewater samples (passive Moore swabs, grab samples, and sediment from drainage ditches) in Come, Benin and Timiri and Jawadhu Hills in Tamil Nadu, India. We detected STH in soil (India = 32/95, Benin = 39/121) and wastewater (India = 24/60, Benin = 8/64) with a detection frequency across all sample types of 36% in India and 25% in Benin. We evaluated which sample locations and types allowed for more sensitive detection of STH DNA and determined that STH prevalence varied by sample site but did not vary significantly within a given sample site location (e.g., samples collected from multiple locations within one market). Further, we determined that wastewater sediment samples outperformed grab and Moore swab sample types for STH detection. Finally, we expanded our methods to include detection of other enteric pathogens using multiplexed qPCR for wastewater samples. Our results establish sampling strategies for environmental and wastewater surveillance of a wide range of enteric pathogens in settings without networked sanitation.
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