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Orally active bivalent VHH construct prevents proliferation of F4+ enterotoxigenic Escherichia coli in weaned piglets

Berthe Katrine Fiil, Sandra Wingaard Thrane, Michael Jakob Pichler, Tiia Kittilä, Line Ledsgaard, Shirin Ahmadi, Grith Miriam Maigaard Hermansen, Lars Jelsbak, Charlotte Lauridsen, Susanne Brix, Andreas H. Laustsen

2022iScience26 citationsDOIOpen Access PDF

Abstract

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.

Topics & Concepts

Enterotoxigenic Escherichia coliMicrobiologyFimbriaAntimicrobialEscherichia coliBiologyAntibioticsAntibiotic resistanceBivalent (engine)ChemistryEnterotoxinBiochemistryGeneOrganic chemistryMetalClostridium difficile and Clostridium perfringens researchBacteriophages and microbial interactionsAntibiotic Resistance in Bacteria
Orally active bivalent VHH construct prevents proliferation of F4+ enterotoxigenic Escherichia coli in weaned piglets | Litcius