Anthropogenic influences on Rhodnius ecuadoriensis populations and nesting behaviors in sylvatic areas of southern ecuador.

IF 3.4 3区 医学 Q2 INFECTIOUS DISEASES
Jazive Esparza-Carate, Soledad Santillán-Guayasamín, César A Yumiseva, Juan José Bustillos, Mario J Grijalva, Sereno Denis, Anita G Villacís
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引用次数: 0

Abstract

Background: Chagas disease, caused by the parasite Trypanosoma cruzi, remains a major public health concern. While Rhodnius ecuadoriensis, a key vector, is traditionally sylvatic, environmental disturbances have driven its adaptation to human-influenced habitats. This study explores a novel factor: how anthropogenic waste affects vector ecology by altering nest compositions. Unlike prior research, this study examines whether human-derived materials in nests influence triatomine colonization. Given rising pollution, particularly post-COVID-19, understanding its role in disease transmission is essential for developing innovative vector control strategies.

Methods: Nest records were collected and analyzed in 2018, 2022, and 2023, across eight communities in Loja province, Ecuador. Nests were categorized as peridomestic if found < 30 m from a house and sylvatic if > 30 m away. The number of insects found in these nests was quantified using entomological indices. Pearson correlation analysis was applied to assess relationships between nest location and the presence of anthropogenic materials.

Results: A total of 389 nests were examined, yielding 1,089 individuals of Rhodnius ecuadoriensis (including both nymphs and adults). The infestation index in peridomestic areas dramatically decreased from 33.3% in 2018 to 0% in 2022, highlighting an intriguing temporal shift that warrants further investigation. In contrast, sylvatic areas showed fluctuating infestation rates (27.5% in 2018, 16.5% in 2022, and 22.2% in 2023). The study uniquely identified a significant association between triatomine infestation and mammal nests, with 50.1% of infested nests located within mammal habitats. Notably, 35.2% of these nests contained anthropogenic materials, particularly near human-altered landscapes such as roads and paths. The weak to moderate negative correlation between the presence of anthropogenic materials and proximity to roads or rivers (r = -0.361, p = 0.039) highlights an innovative exploration of the influence of human environmental changes on vector ecology.

Conclusions: This study offers a novel perspective on the dual impact of increasing pollution levels on wildlife. It highlights how anthropogenic waste not only reduces vector populations but also increases mortality rates through entanglement in waste materials. These findings underscore the urgent need for environmental education programs focused on waste management within local communities. Furthermore, the study paves the way for further research to assess the rate of T. cruzi infection in relation to environmental and anthropogenic factors, offering a critical foundation for understanding and potentially mitigating Chagas disease transmission.

人为因素对厄瓜多尔南部森林地区厄瓜多尔红齿鹬种群和筑巢行为的影响。
背景:由克氏锥虫寄生虫引起的恰加斯病仍然是一个主要的公共卫生问题。虽然主要病媒厄瓜多尔红蝇(Rhodnius ecuadoriensis)传统上生活在森林中,但环境干扰促使其适应受人类影响的栖息地。本研究探讨了一个新的因素:人为废物如何通过改变巢的组成来影响媒介生态。与先前的研究不同,本研究考察了巢穴中人类来源的材料是否会影响锥蝽的定植。鉴于污染日益严重,特别是在2019冠状病毒病之后,了解其在疾病传播中的作用对于制定创新的病媒控制战略至关重要。方法:收集并分析厄瓜多尔洛哈省8个社区2018年、2022年和2023年的巢记录。如果在30米外发现巢穴,则被归类为围家巢。利用昆虫学指标对巢内昆虫的数量进行了量化。应用Pearson相关分析来评估巢址与人为物质存在之间的关系。结果:共检查了389个巢穴,产生了1089只厄瓜多尔红蝶(包括若虫和成虫)。住宅周边地区的虫害指数从2018年的33.3%急剧下降到2022年的0%,突出了一个有趣的时间变化,值得进一步调查。相比之下,森林地区的侵扰率波动较大(2018年为27.5%,2022年为16.5%,2023年为22.2%)。该研究独特地确定了triatomine侵扰与哺乳动物巢穴之间的显著关联,50.1%的受感染巢穴位于哺乳动物栖息地。值得注意的是,这些巢穴中有35.2%含有人为物质,特别是在人类改变的景观(如道路和小径)附近。人为物质的存在与靠近道路或河流之间的弱至中度负相关(r = -0.361, p = 0.039)突出了人类环境变化对媒介生态学影响的创新探索。结论:本研究为研究日益严重的污染对野生动物的双重影响提供了一个新的视角。它强调了人为废物如何不仅减少病媒种群,而且通过废物缠绕增加死亡率。这些发现强调了迫切需要在当地社区开展侧重于废物管理的环境教育项目。此外,该研究为进一步研究评估克氏锥虫感染率与环境和人为因素的关系铺平了道路,为了解和潜在地减轻恰加斯病的传播提供了重要基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BMC Infectious Diseases
BMC Infectious Diseases 医学-传染病学
CiteScore
6.50
自引率
0.00%
发文量
860
审稿时长
3.3 months
期刊介绍: BMC Infectious Diseases is an open access, peer-reviewed journal that considers articles on all aspects of the prevention, diagnosis and management of infectious and sexually transmitted diseases in humans, as well as related molecular genetics, pathophysiology, and epidemiology.
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