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Protecting the piglet gut microbiota against ETEC-mediated post-weaning diarrhoea using specific binding proteins.

Timothy Patrick JenkinsNorbert ÁcsEmma Wenzel ArendrupAbbie SwiftÁgnes DuzsIoanna ChatzigiannidouMichael Jakob PichlerTiia KittiläLaura PeacheyLone GramNuria CanibeAndreas Hougaard LaustsenSusanne B PedersenSandra Wingaard Thrane
Published in: NPJ biofilms and microbiomes (2024)
Post-weaning diarrhoea (PWD) in piglets presents a widespread problem in industrial pig production and is often caused by enterotoxigenic E. coli (ETEC) strains. Current solutions, such as antibiotics and medicinal zinc oxide, are unsustainable and are increasingly being prohibited, resulting in a dire need for novel solutions. Thus, in this study, we propose and evaluate a protein-based feed additive, comprising two bivalent heavy chain variable domain (V H H) constructs (V H H-(GGGGS) 3 -V H H, BL1.2 and BL2.2) as an alternative solution to manage PWD. We demonstrate in vitro that these constructs bind to ETEC toxins and fimbriae, whilst they do no affect bacterial growth rate. Furthermore, in a pig study, we show that oral administration of these constructs after ETEC challenge reduced ETEC proliferation when compared to challenged control piglets (1-2 log 10 units difference in gene copies and bacterial count/g faeces across day 2-7) and resulted in week 1 enrichment of three bacterial families (Prevotellaceae (estimate: 1.12 ± 0.25, q = 0.0054), Lactobacillaceae (estimate: 2.86 ± 0.52, q = 0.0012), and Ruminococcaceae (estimate: 0.66 ± 0.18, q = 0.049)) within the gut microbiota that appeared later in challenged control piglets, thus pointing to an earlier transition towards a more mature gut microbiota. These data suggest that such V H H constructs may find utility in industrial pig production as a feed additive for tackling ETEC and reducing the risk of PWD in piglet populations.
Keyphrases
  • escherichia coli
  • heavy metals
  • clinical trial
  • genome wide
  • dna methylation
  • copy number
  • peripheral blood
  • binding protein
  • acute respiratory distress syndrome