Contact Networks of Small Mammals Highlight Potential Transmission Foci of Mammarenavirus lassaense.

IF 1.6 4区 医学 Q3 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH
David Simons, Ravi Goyal, Umaru Bangura, Rory Gibb, Ben Rushton, Dianah Sondufu, Joyce Lamin, James Koninga, Momoh Foday, Mike Dawson, Joseph Lahai, Rashid Ansumana, Elisabeth Fichet-Calvet, Richard Kock, Deborah Watson-Jones, Kate E Jones
{"title":"Contact Networks of Small Mammals Highlight Potential Transmission Foci of Mammarenavirus lassaense.","authors":"David Simons, Ravi Goyal, Umaru Bangura, Rory Gibb, Ben Rushton, Dianah Sondufu, Joyce Lamin, James Koninga, Momoh Foday, Mike Dawson, Joseph Lahai, Rashid Ansumana, Elisabeth Fichet-Calvet, Richard Kock, Deborah Watson-Jones, Kate E Jones","doi":"10.4269/ajtmh.25-0120","DOIUrl":null,"url":null,"abstract":"<p><p>Lassa fever (LASV; Mammarenavirus lassaense) is an endemic zoonosis in West Africa. Human infections arise from rodent-to-human transmission, primarily from the synanthropic reservoir Mastomys natalensis (M. natalensis). In Sierra Leone, small-mammal communities vary across land-use gradients, shaping LASV transmission risk. How anthropogenic environments facilitate the rodent-rodent interactions remains poorly understood. Small mammals were sampled over 43,266 trap nights in Sierra Leone's LASV-endemic Eastern Province, detecting 684 rodents and shrews. To assess potential transmission, space-sharing networks were constructed from co-trapping events within species-specific home range radii. Shared space use was approximated in these networks, enabling the comparison of encounter patterns across habitats. Network topology varied significantly by land use. Village networks were the most connected (highest average degree), whereas agricultural communities supported the most species (higher rarefied richness) and were the most fragmented (higher modularity). Notably, the probability of intraspecific space sharing among M. natalensis was highest in agricultural settings, suggesting that land use modulates key intraspecific transmission pathways. Lassa fever seroprevalence was 5.7% community-wide, with antibodies detected in nine species. No statistically significant association was found between overall seroprevalence and land use or aggregate network structure (mean degree). However, predictive modeling for M. natalensis indicated that a higher individual degree is associated with seropositivity, suggesting complex, scale-dependent relationships. These findings reveal that simple ecological drivers do not fully explain LASV exposure, highlighting the importance of species-specific behaviors (i.e., M. natalensis clustering in agriculture) and the multihost serological landscape in assessing transmission risk.</p>","PeriodicalId":7752,"journal":{"name":"American Journal of Tropical Medicine and Hygiene","volume":" ","pages":""},"PeriodicalIF":1.6000,"publicationDate":"2026-04-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"American Journal of Tropical Medicine and Hygiene","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.4269/ajtmh.25-0120","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH","Score":null,"Total":0}
引用次数: 0

Abstract

Lassa fever (LASV; Mammarenavirus lassaense) is an endemic zoonosis in West Africa. Human infections arise from rodent-to-human transmission, primarily from the synanthropic reservoir Mastomys natalensis (M. natalensis). In Sierra Leone, small-mammal communities vary across land-use gradients, shaping LASV transmission risk. How anthropogenic environments facilitate the rodent-rodent interactions remains poorly understood. Small mammals were sampled over 43,266 trap nights in Sierra Leone's LASV-endemic Eastern Province, detecting 684 rodents and shrews. To assess potential transmission, space-sharing networks were constructed from co-trapping events within species-specific home range radii. Shared space use was approximated in these networks, enabling the comparison of encounter patterns across habitats. Network topology varied significantly by land use. Village networks were the most connected (highest average degree), whereas agricultural communities supported the most species (higher rarefied richness) and were the most fragmented (higher modularity). Notably, the probability of intraspecific space sharing among M. natalensis was highest in agricultural settings, suggesting that land use modulates key intraspecific transmission pathways. Lassa fever seroprevalence was 5.7% community-wide, with antibodies detected in nine species. No statistically significant association was found between overall seroprevalence and land use or aggregate network structure (mean degree). However, predictive modeling for M. natalensis indicated that a higher individual degree is associated with seropositivity, suggesting complex, scale-dependent relationships. These findings reveal that simple ecological drivers do not fully explain LASV exposure, highlighting the importance of species-specific behaviors (i.e., M. natalensis clustering in agriculture) and the multihost serological landscape in assessing transmission risk.

小型哺乳动物的接触网络突出了潜在的哺乳病毒拉沙病传播焦点。
拉沙热是西非的一种地方性人畜共患病。人类感染是由啮齿动物向人类传播引起的,主要是由natalensis (m.a natalensis)共存宿主。在塞拉利昂,小型哺乳动物群落因土地利用梯度而异,形成了LASV传播的风险。人类环境如何促进啮齿动物与啮齿动物之间的相互作用仍然知之甚少。在塞拉利昂lasv流行的东部省,在43266个陷阱夜对小型哺乳动物进行了采样,发现了684只啮齿动物和鼩鼱。为了评估潜在的传播,在特定物种的栖息地半径内,通过共同捕获事件构建了空间共享网络。在这些网络中,共享空间的使用是近似的,从而可以比较不同栖息地之间的相遇模式。网络拓扑结构因土地利用而显著不同。村庄网络连接程度最高(平均程度最高),而农业群落支持的物种最多(稀薄丰富度较高),且最分散(模块化程度较高)。值得注意的是,在农业环境下,natalensis种内空间共享的可能性最高,这表明土地利用调节了关键的种内传播途径。全社区拉沙热血清阳性率为5.7%,在9种动物中检测到抗体。总体血清阳性率与土地利用或总体网络结构(平均程度)之间没有统计学上的显著关联。然而,对M. natalensis的预测模型表明,较高的个体程度与血清阳性相关,表明复杂的规模依赖关系。这些发现表明,简单的生态驱动因素并不能完全解释LASV暴露,这突出了物种特异性行为(即农业中的纳塔勒氏芽孢杆菌聚集)和多宿主血清学景观在评估传播风险方面的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
American Journal of Tropical Medicine and Hygiene
American Journal of Tropical Medicine and Hygiene 医学-公共卫生、环境卫生与职业卫生
CiteScore
6.20
自引率
3.00%
发文量
508
审稿时长
3 months
期刊介绍: The American Journal of Tropical Medicine and Hygiene, established in 1921, is published monthly by the American Society of Tropical Medicine and Hygiene. It is among the top-ranked tropical medicine journals in the world publishing original scientific articles and the latest science covering new research with an emphasis on population, clinical and laboratory science and the application of technology in the fields of tropical medicine, parasitology, immunology, infectious diseases, epidemiology, basic and molecular biology, virology and international medicine. The Journal publishes unsolicited peer-reviewed manuscripts, review articles, short reports, images in Clinical Tropical Medicine, case studies, reports on the efficacy of new drugs and methods of treatment, prevention and control methodologies,new testing methods and equipment, book reports and Letters to the Editor. Topics range from applied epidemiology in such relevant areas as AIDS to the molecular biology of vaccine development. The Journal is of interest to epidemiologists, parasitologists, virologists, clinicians, entomologists and public health officials who are concerned with health issues of the tropics, developing nations and emerging infectious diseases. Major granting institutions including philanthropic and governmental institutions active in the public health field, and medical and scientific libraries throughout the world purchase the Journal. Two or more supplements to the Journal on topics of special interest are published annually. These supplements represent comprehensive and multidisciplinary discussions of issues of concern to tropical disease specialists and health issues of developing countries
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书