产肠毒素大肠杆菌
微生物学
伞
抗菌剂
大肠杆菌
抗生素
生物
抗生素耐药性
二价(发动机)
化学
肠毒素
生物化学
基因
有机化学
金属
作者
Berthe Katrine Fiil,Sandra Wingaard Thrane,M.J. Pichler,Tiia Kittilä,Line Ledsgaard,Shirin Ahmadi,Grith Miriam Maigaard Hermansen,Lars Jelsbak,Charlotte Lauridsen,Susanne Brix,José María Gutiérrez
出处
期刊:iScience
[Cell Press]
日期:2022-04-01
卷期号:25 (4): 104003-104003
被引量:5
标识
DOI:10.1016/j.isci.2022.104003
摘要
A major challenge in industrial pig production is the prevalence of post-weaning diarrhea (PWD) in piglets, often caused by enterotoxigenic Escherichia coli (ETEC). The increased use of antibiotics and zinc oxide to treat PWD has raised global concerns regarding antimicrobial resistance development and environmental pollution. Still, alternative treatments targeting ETEC and counteracting PWD are largely lacking. Here, we report the design of a pH, temperature, and protease-stable bivalent VHH-based protein BL1.2 that cross-links a F4+ ETEC model strain by selectively binding to its fimbriae. This protein inhibits F4+ ETEC adhesion to porcine epithelial cells ex vivo and decreases F4+ ETEC proliferation when administrated as a feed additive to weaned F4+ ETEC challenged piglets. These findings highlight the potential of a highly specific bivalent VHH-based feed additive in effectively delimiting pathogenic F4+ ETEC bacteria proliferation in piglets and may represent a sustainable solution for managing PWD while circumventing antimicrobial resistance development.
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