Determinants of Campylobacter species diversity in infants and association with family members, livestock, and household environments in rural Eastern Ethiopia.

IF 4.3 3区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY
Amanda Ojeda, Loïc Deblais, Bahar Mummed, Mussie Brhane, Kedir A Hassen, Belisa Usmael Ahmedo, Yenenesh Demisie Weldesenbet, Dehao Chen, Xiaolong Li, Cyrus Saleem, Mark J Manary, Luiz F W Roesch, Sarah L McKune, Arie H Havelaar, Gireesh Rajashekara
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引用次数: 0

Abstract

Background: Campylobacter infections pose a significant challenge in low- and middle-income countries, contributing to child mortality. Campylobacter is linked to acute gastrointestinal illness and severe long-term consequences, including environmental enteric dysfunction (EED) and stunting. In 2018, our cross-sectional study in Ethiopia detected Campylobacter in 88% of stools from children aged 12-15 months, with an average of 11 species per stool using meta-total RNA sequencing. Building on these findings, we conducted a longitudinal study (December 2020-June 2022) to investigate Campylobacter colonization of infants and identify reservoirs and risk factors in rural eastern Ethiopia.

Results: After a preliminary screening of 15 Campylobacter species using species-specific quantitative PCR, we analyzed four target species in 2045 samples from infants (first month to just one year of life) and biannual samples from mothers, siblings, and livestock (goats, cattle, sheep, and chickens). Candidatus C. infans (41%), C. jejuni (26%), and C. upsaliensis (13%) were identified as the predominant in the infant gut. Colonization of C. infans and C.jejuni increased (C. infans: 0.85%, C. jejuni-0.98% increase/ day in the odds of colonization) and abundance (P = 0.027, 0.024) with age. Enteric symptoms were strongly associated with C. infans (diarrhea: OR = 2.02 [95%CI: 35%,100%]; fever: OR = 1.62 [95%CI: 14%, 83%]) and C. jejuni (diarrhea: OR = 2.29 [95%CI: 46%,100%], fever: OR = 2.53 [95%CI: 56%,100%]). Based on linear mixed models, we found elevated cumulative loads of C. infans load in infants (especially females OR = 1.5 [95%CI: 10%, 67%]), consuming raw milk (OR = 2.3 [95%CI: 24%,100%]) or those exposed to areas contaminated with animal droppings (OR = 1.6 [95%CI: 7%,93%]), while C. jejuni cumulative loads were higher in infants ingesting soil or animal feces (OR = 2.2 [95%CI: 23%,100%]). C. infans was also prevalent in siblings (56%) and mothers (45%), whereas C. jejuni was common in chickens (38%) and small ruminants (goats 27%, sheep 21%).

Conclusions: Campylobacter was highly prevalent in rural Ethiopian infants. C. infans was primarily associated with human hosts, and C. jejuni was mainly linked to zoonotic sources. Our findings emphasize the need for targeted interventions addressing environmental, dietary, and behavioral factors to reduce Campylobacter transmission in resource-limited settings.

埃塞俄比亚东部农村婴儿弯曲杆菌种类多样性的决定因素及其与家庭成员、牲畜和家庭环境的关系
背景:弯曲杆菌感染在低收入和中等收入国家构成重大挑战,导致儿童死亡。弯曲杆菌与急性胃肠道疾病和严重的长期后果有关,包括环境肠功能障碍(EED)和发育迟缓。2018年,我们在埃塞俄比亚进行的横断面研究在12-15个月大的儿童粪便中检测到88%的弯曲杆菌,使用元总RNA测序,平均每个粪便中有11种弯曲杆菌。在这些发现的基础上,我们进行了一项纵向研究(2020年12月至2022年6月),以调查弯曲杆菌在埃塞俄比亚东部农村的定植情况,并确定宿主和危险因素。结果:在使用物种特异性定量PCR对15种弯曲杆菌进行初步筛选后,我们分析了2045份婴儿(1个月至1岁)样本中的4种目标物种,以及来自母亲、兄弟姐妹和牲畜(山羊、牛、绵羊和鸡)的两年一次的样本。在婴儿肠道中,候选C.婴儿(41%)、C.空肠(26%)和C. upsaliensis(13%)为优势菌群。随着年龄的增长,婴儿弧菌和空肠弧菌的定殖率(婴儿弧菌:0.85% / d,空肠弧菌-0.98% / d)和丰度(P = 0.027, 0.024)均有所增加。肠道症状与婴儿乳杆菌密切相关(腹泻:OR = 2.02 [95%CI: 35%,100%];发烧:或= 1.62 (95% ci: 14%、83%)空肠)和c(腹泻:或者= 2.29 (95% ci: 46%、100%),发热:或= 2.53 (95% ci: 56%、100%))。基于线性混合模型,我们发现,食用原料奶(OR = 2.3 [95%CI: 24%,100%])或暴露于动物粪便污染地区的婴儿(OR = 1.6 [95%CI: 7%,93%])的婴儿(尤其是雌性OR = 1.5 [95%CI: 10%, 67%])的婴儿(OR = 1.5 [95%CI: 24%,100%])的婴儿(OR = 2.2 [95%CI: 23%,100%])的婴儿(C. jejuni)的累积负荷较高。婴儿梭菌在兄弟姐妹(56%)和母亲(45%)中也很常见,而空肠梭菌在鸡(38%)和小反刍动物(山羊27%,绵羊21%)中很常见。结论:弯曲杆菌在埃塞俄比亚农村婴儿中高度流行。婴儿梭菌主要与人类宿主有关,空肠梭菌主要与人畜共患源有关。我们的研究结果强调需要针对环境、饮食和行为因素进行有针对性的干预,以在资源有限的环境中减少弯曲杆菌的传播。
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来源期刊
Gut Pathogens
Gut Pathogens GASTROENTEROLOGY & HEPATOLOGY-MICROBIOLOGY
CiteScore
7.70
自引率
2.40%
发文量
43
期刊介绍: Gut Pathogens is a fast publishing, inclusive and prominent international journal which recognizes the need for a publishing platform uniquely tailored to reflect the full breadth of research in the biology and medicine of pathogens, commensals and functional microbiota of the gut. The journal publishes basic, clinical and cutting-edge research on all aspects of the above mentioned organisms including probiotic bacteria and yeasts and their products. The scope also covers the related ecology, molecular genetics, physiology and epidemiology of these microbes. The journal actively invites timely reports on the novel aspects of genomics, metagenomics, microbiota profiling and systems biology. Gut Pathogens will also consider, at the discretion of the editors, descriptive studies identifying a new genome sequence of a gut microbe or a series of related microbes (such as those obtained from new hosts, niches, settings, outbreaks and epidemics) and those obtained from single or multiple hosts at one or different time points (chronological evolution).
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