Cameron Mary M, Acosta-Serrano Alvaro, Bern Caryn, Boelaert Marleen, den Boer Margriet, Burza Sakib, Chapman Lloyd A C, Chaskopoulou Alexandra, Coleman Michael, Courtenay Orin, Croft Simon, Das Pradeep, Dilger Erin, Foster Geraldine, Garlapati Rajesh, Haines Lee, Harris Angela, Hemingway Janet, Hollingsworth T Déirdre, Jervis Sarah, Medley Graham, Miles Michael, Paine Mark, Picado Albert, Poché Richard, Ready Paul, Rogers Matthew, Rowland Mark, Sundar Shyam, de Vlas Sake J, Weetman David
London School of Hygiene and Tropical Medicine, Keppel Street, London, WC1E 7HT, UK.
Liverpool School of Tropical Medicine, Pembroke Place, Liverpool, L3 5QA, UK.
Parasit Vectors. 2016 Jan 27;9:25. doi: 10.1186/s13071-016-1309-8.
Visceral Leishmaniasis (VL) is a neglected vector-borne disease. In India, it is transmitted to humans by Leishmania donovani-infected Phlebotomus argentipes sand flies. In 2005, VL was targeted for elimination by the governments of India, Nepal and Bangladesh by 2015. The elimination strategy consists of rapid case detection, treatment of VL cases and vector control using indoor residual spraying (IRS). However, to achieve sustained elimination of VL, an appropriate post elimination surveillance programme should be designed, and crucial knowledge gaps in vector bionomics, human infection and transmission need to be addressed. This review examines the outstanding knowledge gaps, specifically in the context of Bihar State, India.The knowledge gaps in vector bionomics that will be of immediate benefit to current control operations include better estimates of human biting rates and natural infection rates of P. argentipes, with L. donovani, and how these vary spatially, temporally and in response to IRS. The relative importance of indoor and outdoor transmission, and how P. argentipes disperse, are also unknown. With respect to human transmission it is important to use a range of diagnostic tools to distinguish individuals in endemic communities into those who: 1) are to going to progress to clinical VL, 2) are immune/refractory to infection and 3) have had past exposure to sand flies.It is crucial to keep in mind that close to elimination, and post-elimination, VL cases will become infrequent, so it is vital to define what the surveillance programme should target and how it should be designed to prevent resurgence. Therefore, a better understanding of the transmission dynamics of VL, in particular of how rates of infection in humans and sand flies vary as functions of each other, is required to guide VL elimination efforts and ensure sustained elimination in the Indian subcontinent. By collecting contemporary entomological and human data in the same geographical locations, more precise epidemiological models can be produced. The suite of data collected can also be used to inform the national programme if supplementary vector control tools, in addition to IRS, are required to address the issues of people sleeping outside.
内脏利什曼病(VL)是一种被忽视的媒介传播疾病。在印度,它通过感染杜氏利什曼原虫的银足白蛉传播给人类。2005年,印度、尼泊尔和孟加拉国政府将到2015年消除内脏利什曼病作为目标。消除战略包括快速病例检测、治疗内脏利什曼病病例以及使用室内滞留喷洒(IRS)进行病媒控制。然而,为了实现内脏利什曼病的持续消除,应设计适当的消除后监测计划,并解决病媒生物学、人类感染和传播方面的关键知识空白。本综述探讨了突出的知识空白,特别是在印度比哈尔邦的背景下。病媒生物学方面的知识空白将对当前的控制行动立即产生帮助,包括更准确地估计银足白蛉的人叮咬率和自然感染率,以及这些率如何在空间、时间上变化以及对室内滞留喷洒的反应。室内和室外传播的相对重要性以及银足白蛉如何扩散也尚不清楚。关于人类传播,重要的是使用一系列诊断工具将流行社区中的个体区分为:1)即将发展为临床内脏利什曼病的个体,2)对感染具有免疫/抵抗力的个体,3)过去曾接触过白蛉的个体。必须牢记,在内脏利什曼病接近消除和消除之后,病例将变得罕见,因此至关重要的是确定监测计划应针对的目标以及应如何设计以防止疾病复发。因此,需要更好地了解内脏利什曼病的传播动态,特别是人类和白蛉感染率如何相互作用,以指导内脏利什曼病的消除工作并确保在印度次大陆持续消除该疾病。通过在相同地理位置收集当代昆虫学和人类数据,可以生成更精确的流行病学模型。如果除了室内滞留喷洒之外还需要补充病媒控制工具来解决人们睡在户外的问题,则收集的数据集还可用于为国家计划提供信息。