Takagi Hidekazu, Yahathugoda Thishan C, Tojo Bumpei, Rathnapala Upeksha L, Nagaoka Fumiaki, Weerasooriya Mirani V, Itoh Makoto
1Department of Microbiology & Immunology, Aichi Medical University School of Medicine, Nagakute, Aichi 480-1195 Japan.
3Filariasis Research Training and Service Unit (FRTSU), Department of Parasitology, Faculty of Medicine, University of Ruhuna, Galle, Sri Lanka.
Trop Med Health. 2019 Jun 13;47:39. doi: 10.1186/s41182-019-0166-5. eCollection 2019.
Surveillance of hidden foci or resurgence of the bancroftian filariasis has high priority to maintain the elimination status in Sri Lanka. For the surveillance, two methods were applied in Matotagama, Matara, Sri Lanka; (i) molecular xenomonitoring (MX) by PCR to detect parasite DNA in the vector, () and (ii) survey of anti-filarial IgG4 in urine samples from schoolchildren.
Mosquitoes were collected monthly from index houses for 17 months (2013 to 2014) to confirm the existence of bancroftian parasite. Index houses in Matotagama had recorded microfilaria-positive cases in the recent past. Five schools were selected considering Matotagama as the catchment area and all students who presented on the day were tested for urine anti-filarial IgG4 in 2015. DNA in . pools were found in 14 of 17 months studied and ranged between 0 and 1.4%. The MX rate was greatly increased at least two times in the year following the driest months (March, August). A total of 735 schoolchildren were tested for urine anti-filarial IgG4. Three schools located closer to the MX area had higher positive rates, 3.4%, 3.6%, and 6.6%. Both highest positive rates of MX and urine were located in a nearer vicinity.
Monthly collections to study lymphatic filariasis (LF) transmission by MX was conducted for the first time in Sri Lanka. We observed that the filarial DNA-positive rate had an association with seasonal cycle of precipitation. More than 1% filarial DNA and > 5% anti-filarial antibody rates confirmed ongoing transmission in Matotagama. The combination of two non-invasive surveys, the urine anti-filarial IgG4 levels of schoolchildren and MX of vector mosquitoes, would be a convenient package to monitor the ongoing transmission (hotspots) of LF in the surveillance.
监测班氏丝虫病的隐匿病灶或复发情况对于斯里兰卡维持消除状态至关重要。在斯里兰卡马特勒的马托塔加马,采用了两种监测方法:(i) 通过聚合酶链反应(PCR)进行分子异体监测(MX)以检测病媒中的寄生虫DNA,以及(ii) 对学童尿液样本中的抗丝虫IgG4进行检测。
在17个月(2013年至2014年)内每月从指示家庭收集蚊子,以确认班氏寄生虫的存在。马托塔加马的指示家庭近期记录有微丝蚴阳性病例。以马托塔加马为集水区选择了5所学校,2015年对当日到校的所有学生进行尿液抗丝虫IgG4检测。在研究的17个月中的14个月里,在蚊群中发现了DNA,范围在0%至1.4%之间。在最干燥月份(3月、8月)后的一年中,MX率至少增加了两倍。总共对735名学童进行了尿液抗丝虫IgG4检测。距离MX区域较近的三所学校阳性率较高,分别为3.4%、3.6%和6.6%。MX和尿液的最高阳性率都位于较近区域。
斯里兰卡首次每月进行收集以通过MX研究淋巴丝虫病(LF)传播。我们观察到丝虫DNA阳性率与降水季节周期有关。马托塔加马超过1%的丝虫DNA和>5%的抗丝虫抗体率证实存在持续传播。学童尿液抗丝虫IgG4水平和病媒蚊子MX这两种非侵入性调查方法相结合,将是监测LF在监测中的持续传播(热点)的便捷组合。