Characterization of clumpy adhesion of Escherichia coli to human cells and associated factors influencing antibiotic sensitivity

Author:

Khan Muhammad Moman1ORCID,Sidorczuk Katarzyna2ORCID,Becker Juliane1,Aleksandrowicz Adrianna3,Baraniewicz Karolina34,Ludwig Christina5,Ali Aamir6ORCID,Kingsley Robert A.7ORCID,Schierack Peter1ORCID,Kolenda Rafał37ORCID

Affiliation:

1. Institute for Biotechnology, Brandenburg University of Technology (BTU) Cottbus-Senftenberg, Senftenberg, Germany

2. Department of Bioinformatics and Genomics, Faculty of Biotechnology, University of Wrocław, Wrocław, Poland

3. Department of Biochemistry and Molecular Biology, Faculty of Veterinary Medicine, Wrocław University of Environmental and Life Sciences, Wrocław, Poland

4. Department of Microbiology, Institute of Genetics and Microbiology, University of Wrocław, Wrocław, Poland

5. Bavarian Center for Biomolecular Mass Spectrometry (BayBioMS), School of Life Sciences, Technical University Munich (TUM), Munich, Germany

6. National Institute for Biotechnology and Genetic Engineering College, Pakistan Institute of Engineering and Applied Sciences (NIBGE-C, PIEAS), Faisalabad, Pakistan

7. Quadram Institute Biosciences, Norwich Research Park, Norwich, United Kingdom

Abstract

ABSTRACT Escherichia coli intestinal infection pathotypes are characterized by distinct adhesion patterns, including the recently described clumpy adhesion phenotype. Here, we identify and characterize the genetic factors contributing to the clumpy adhesion of E. coli strain 4972. In this strain, the transcriptome and proteome of adhered bacteria were found to be distinct from planktonic bacteria in the supernatant. A total of 622 genes in the transcriptome were differentially expressed in bacteria present in clumps relative to the planktonic bacteria. Seven genes targeted for disruption had variable distribution in different pathotypes and nonpathogenic E. coli, with the pilV and spnT genes being the least frequent or absent from most groups. Deletion (Δ) of five differentially expressed genes, flgH , ffp , pilV , spnT, and yggT, affected motility, adhesion, or antibiotic stress. Δ flgH exhibited 80% decrease and Δ yggT depicted 184% increase in adhesion, and upon complementation, adhesion was significantly reduced to 13%. Δ flgH lost motility and was regenerated when complemented, whereas Δ ffp had significantly increased motility, and reintroduction of the same gene reduced it to the wild-type level. The clumps produced by Δ ffp and Δ spnT were more resistant and protected the bacteria, with Δ spnT showing the best clump formation in terms of ampicillin stress protection. Δ yggT had the lowest tolerance to gentamicin, where the antibiotic stress completely eliminated the bacteria. Overall, we were able to investigate the influence of clump formation on cell surface adhesion and antimicrobial tolerance, with the contribution of several factors crucial to clump formation on susceptibility to the selected antibiotics. IMPORTANCE The study explores a biofilm-like clumpy adhesion phenotype in Escherichia coli, along with various factors and implications for antibiotic susceptibility. The phenotype permitted the bacteria to survive the onslaught of high antibiotic concentrations. Profiles of the transcriptome and proteome allowed the differentiation between adhered bacteria in clumps and planktonic bacteria in the supernatant. The deletion mutants of genes differentially expressed between adhered and planktonic bacteria, i.e., flgH , ffp , pilV , spnT , and yggT, and respective complementations in trans cemented their roles in multiple capacities. ffp , an uncharacterized gene, is involved in motility and resistance to ampicillin in a clumpy state. The work also affirms for the first time the role of the yggT gene in adhesion and its involvement in susceptibility against another aminoglycoside antibiotic, i.e., gentamicin. Overall, the study contributes to the mechanisms of biofilm-like adhesion phenotype and understanding of the antimicrobial therapy failures and infections of E. coli .

Publisher

American Society for Microbiology

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