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蛋白质营养不良促进肠道被高抗性菌定植。

Protein Malnutrition Facilitates Intestinal Colonization with Highly Resistant .

作者信息

Holowka Thomas, Santiago Veronica Feijoli, Xiao Jamie, Liccione Mera F, Bimagambetov Alisher, Walsh Kenneth, Arnold Jason W, Marimuthu Kalisvar, Ng Oon Tek, Swann Jonathan R, van Duin David, Bartelt Luther A

机构信息

Division of Infectious Diseases, Department of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.

School of Human Development and Health, Faculty of Medicine, University of Southampton, Southampton, United Kingdom.

出版信息

bioRxiv. 2025 Jul 21:2025.07.21.665917. doi: 10.1101/2025.07.21.665917.

Abstract

Pediatric infections with Highly Resistant Enterobacterales (HRE), including resistant to 3-generation cephalosporins and/or carbapenems, disproportionately affect low- and middle-income countries where malnutrition is prevalent. The underlying mechanisms linking malnutrition to HRE colonization in children have not been established. In this study we developed a mouse model of pediatric malnutrition and intestinal colonization with clinical isolates of carbapenem-resistant (CR-Kp). Juvenile mice fed a protein-deficient diet (PD) were more susceptible to intestinal colonization after inoculation with human-derived strains of CR-Kp, demonstrating a 3-4 log higher colonization burden in comparison to mice fed a control diet (CD). Colonization in PD-fed mice persisted for up to 6 weeks and CR-Kp were transmitted between PD-fed but not CD-fed cage mates. Antibiotic treatment resulted in similar CR-Kp colonization burdens regardless of diet, suggesting that nutrition-dependent colonization resistance is reliant on an intact microbiota. Secondary bile acids, a product of resident intestinal microbiota, were reduced in PD-fed and antibiotic treated mice and demonstrated an inverse correlation with CR-Kp burden. Secondary bile acids directly inhibited CR-Kp growth , suggesting that a loss of these inhibitory metabolites may mediate malnutrition-induced susceptibility to HRE colonization.

摘要

儿童感染高耐药性肠杆菌科细菌(HRE),包括对第三代头孢菌素和/或碳青霉烯类耐药的细菌,对营养不良普遍存在的低收入和中等收入国家影响尤为严重。营养不良与儿童HRE定植之间的潜在机制尚未明确。在本研究中,我们建立了一个儿童营养不良和肠道定植的小鼠模型,使用碳青霉烯耐药肺炎克雷伯菌(CR-Kp)的临床分离株。喂食蛋白质缺乏饮食(PD)的幼年小鼠在接种人源CR-Kp菌株后更容易发生肠道定植,与喂食对照饮食(CD)的小鼠相比,定植负担高3-4个对数。PD喂养小鼠的定植持续长达6周,CR-Kp在PD喂养而非CD喂养的同笼小鼠之间传播。无论饮食如何,抗生素治疗导致的CR-Kp定植负担相似,这表明营养依赖性定植抗性依赖于完整的微生物群。次级胆汁酸是肠道常驻微生物群的产物,在PD喂养和抗生素治疗的小鼠中减少,并与CR-Kp负担呈负相关。次级胆汁酸直接抑制CR-Kp生长,表明这些抑制性代谢产物的丧失可能介导了营养不良诱导的对HRE定植的易感性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3413/12330750/1f5ddedfae34/nihpp-2025.07.21.665917v1-f0001.jpg

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