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2017年美属萨摩亚登革热病毒感染相关风险因素及蚊媒的鉴定

Identification of risk factors and mosquito vectors associated with dengue virus infection in American Samoa, 2017.

作者信息

Sharp Tyler M, Tufa A John, Cotter Caitlin J, Lozier Matthew J, Santiago Gilberto A, Johnson Stephanie S, Mataia'a Mary, Waterman Stephen H, Muñoz-Jordán Jorge L, Paz-Bailey Gabriela, Hemme Ryan R, Schmaedick Mark A, Anesi Scott

机构信息

Dengue Branch, Centers for Disease Control and Prevention, San Juan, Puerto Rico.

United States Public Health Service, Silver Springs, Maryland, United States of America.

出版信息

PLOS Glob Public Health. 2023 Jul 7;3(7):e0001604. doi: 10.1371/journal.pgph.0001604. eCollection 2023.

Abstract

INTRODUCTION

The first outbreak of dengue in American Samoa was reported in 1911. Sporadic outbreaks have been reported since, as were outbreaks of other pathogens transmitted by Aedes species mosquitoes including Ross River, chikungunya, and Zika viruses. During an outbreak of dengue virus-type 2 (DENV-2) in 2016-2018, we conducted household-based cluster investigations to identify population-specific risk factors associated with infection and performed entomologic surveillance to determine the relative abundance of Ae. aegypti and Ae. polynesiensis.

METHODS AND FINDINGS

We contacted dengue patients who had tested positive for DENV infection and offered them as well as their household members participation in household-based cluster investigations. For those that accepted participation, we also offered participation to residents of households within a 50-meter radius of each case-patient's home. Questionnaires were administered and serum specimens collected for testing by RT-PCR and anti-DENV IgM ELISA. Adult female mosquitoes were aspirated from inside and outside participating households and tested by RT-PCR. We analyzed characteristics associated with DENV infection in bivariate analyses. A total of 226 participants was enrolled from 91 households in 20 clusters. Median age of participants was 34 years (range: <1-94), and 56.2% were female. In total, 7 (3.2%) participants had evidence of DENV infection by IgM ELISA (n = 5) or RT-PCR (n = 2). Factors significantly associated with DENV infection were reporting a febrile illness in the past three months (prevalence ratio: 7.5 [95% confidence interval: 1.9-29.8]) and having a household septic tank (Fisher's Exact Test, p = 0.004). Of 93 Ae. aegypti and 90 Ae. polynesiensis females collected, 90% of Ae. aegypti were collected inside homes whereas 83% of Ae. polynesiensis were collected outside homes. DENV nucleic acid was not detected in any mosquito pools. Sequencing of the DENV-2 from patient specimens identified the Cosmopolitan genotype of DENV-2 and was most closely related to virus detected in the Solomon Islands during 2016.

CONCLUSIONS

This investigation demonstrated that dengue is a continuing risk in American Samoa. Increased frequency of infection among residents with a septic tank suggests a need to investigate whether septic tanks serve as larval habitats for mosquito vectors of DENV in American Samoa. Future efforts should also evaluate the role of Ae. polynesiensis in DENV transmission in the wild.

摘要

引言

美属萨摩亚于1911年首次报告登革热疫情。此后陆续有散发病例报告,同时也有由伊蚊传播的其他病原体引发的疫情,包括罗斯河病毒、基孔肯雅病毒和寨卡病毒。在2016 - 2018年登革热2型病毒(DENV - 2)疫情期间,我们开展了基于家庭的聚集性调查,以确定与感染相关的特定人群风险因素,并进行了昆虫学监测,以确定埃及伊蚊和波利尼西亚伊蚊的相对丰度。

方法与结果

我们联系了登革热病毒感染检测呈阳性的患者,并邀请他们及其家庭成员参与基于家庭的聚集性调查。对于接受参与的人员,我们还邀请了每个病例患者家半径50米范围内家庭的居民参与。我们发放了问卷,并采集血清标本进行逆转录聚合酶链反应(RT - PCR)检测和抗登革热病毒免疫球蛋白M(IgM)酶联免疫吸附测定(ELISA)。从参与调查的家庭内外采集成年雌性蚊子,并通过RT - PCR进行检测。我们在双变量分析中分析了与登革热病毒感染相关的特征。共从20个聚集性区域的91户家庭中招募了226名参与者。参与者的年龄中位数为34岁(范围:<1 - 94岁),56.2%为女性。共有7名(3.2%)参与者通过IgM ELISA(n = 5)或RT - PCR(n = 2)检测出有登革热病毒感染的证据。与登革热病毒感染显著相关的因素包括在过去三个月内报告有发热疾病(患病率比值:7.5 [95%置信区间:1.9 - 29.8])以及家中有化粪池(费舍尔精确检验,p = 0.004)。在采集的93只埃及伊蚊和90只波利尼西亚伊蚊雌性蚊子中,90%的埃及伊蚊是在室内采集的,而83%的波利尼西亚伊蚊是在室外采集的。在任何蚊子样本池中均未检测到登革热病毒核酸。对患者标本中的DENV - 2进行测序,确定为DENV - 2的泛在基因型,并且与2016年在所罗门群岛检测到的病毒最为接近。

结论

本次调查表明,登革热在美属萨摩亚仍然是一个持续存在的风险。化粪池居民感染频率增加表明有必要调查化粪池是否是美属萨摩亚登革热病毒蚊媒的幼虫栖息地。未来的工作还应评估波利尼西亚伊蚊在野外登革热病毒传播中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0cd4/10328243/27eb6240d1f0/pgph.0001604.g001.jpg

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