4.5 Article

The Superior Adherence Phenotype of E. coli O104:H4 is Directly Mediated by the Aggregative Adherence Fimbriae Type I

Journal

VIRULENCE
Volume 12, Issue 1, Pages 346-359

Publisher

TAYLOR & FRANCIS INC
DOI: 10.1080/21505594.2020.1868841

Keywords

Enteroaggregative E. coli; enterohemorrhagic E. coli; AAF; adherence; biofilm; autoaggregation

Funding

  1. European Commission FP7 ANTIGONE contract [278976]
  2. Federal Ministry of Education and Research (BMBF) [01DN19008]
  3. German Research Foundation [SFB1009B4, ME3205/5-1, 276606594]

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The study found differences in adherence properties and pathogenicity between the EHEC outbreak strain O104:H4 and its close relative due to expression of different types of aggregative adherence fimbriae (AAF). Various types of AAF affect bacterial autoaggregation, biofilm formation, and host cell adherence.
Whereas the O104:H4 enterohemorrhagic Escherichia coli (EHEC) outbreak strain from 2011 expresses aggregative adherence fimbriae of subtype I (AAF/I), its close relative, the O104:H4 enteroaggregative Escherichia coli (EAEC) strain 55989, encodes AAF of subtype III. Tight adherence mediated by AAF/I in combination with Shiga toxin 2 production has been suggested to result in the outbreak strain's exceptional pathogenicity. Furthermore, the O104:H4 outbreak strain adheres significantly better to cultured epithelial cells than archetypal EAEC strains expressing different AAF subtypes. To test whether AAF/I expression is associated with the different virulence phenotypes of the outbreak strain, we heterologously expressed AAF subtypes I, III, IV, and V in an AAF-negative EAEC 55989 mutant and compared AAF-mediated phenotypes, incl. autoaggregation, biofilm formation, as well as bacterial adherence to HEp-2 cells. We observed that the expression of all four AAF subtypes promoted bacterial autoaggregation, though with different kinetics. Disturbance of AAF interaction on the bacterial surface via addition of alpha-AAF antibodies impeded autoaggregation. Biofilm formation was enhanced upon heterologous expression of AAF variants and inversely correlated with the autoaggregation phenotype. Co-cultivation of bacteria expressing different AAF subtypes resulted in mixed bacterial aggregates. Interestingly, bacteria expressing AAF/I formed the largest bacterial clusters on HEp-2 cells, indicating a stronger host cell adherence similar to the EHEC O104:H4 outbreak strain. Our findings show that, compared to the closely related O104:H4 EAEC strain 55989, not only the acquisition of the Shiga toxin phage, but also the acquisition of the AAF/I subtype might have contributed to the increased EHEC O104:H4 pathogenicity.

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