» Articles » PMID: 10496928

Functional Characterization of Type IV Pili Expressed on Diarrhea-associated Isolates of Aeromonas Species

Overview
Journal Infect Immun
Date 1999 Sep 25
PMID 10496928
Citations 17
Authors
Affiliations
Soon will be listed here.
Abstract

Our past work has shown that long, flexible type IV pili (single or in bundles) are the predominant pili expressed on fecal isolates of diarrhea-associated species of Aeromonas (Aeromonas veronii biovar sobria and A. caviae). They represent a family of type IV pili which we have designated Bfp (for bundle-forming pili). Reports from Japan suggest that Bfp are intestinal colonization factors. This study presents compelling evidence to support this conclusion. Aeromonas bacteria and/or Bfp purified from a strain of A. veronii biovar sobria were shown to adhere to epithelial and intestinal cell lines, freshly isolated human enterocytes, and fresh and fixed human and rabbit intestinal tissues, as determined by light and electron microscopy and immunohistochemical detection. Removal of Bfp by mechanical means decreased adhesion to cell lines by up to 80%. Purified Bfp blocked adhesion of the test strain to intestinal cells in a dose-dependent manner. Adhesion was also blocked by the Fab fraction of anti-Bfp immunoglobulin G. Moreover, ultrastructural studies (ruthenium red staining and transmission and scanning electron microscopy) demonstrated for the first time that Aeromonas adhesion to human enterocytes is pilus mediated and suggested that Bfp may also promote colonization by forming bacterium-to-bacterium linkages. Bfp-positive isolates examined for type IV pilus-mediated twitching motility in agar and slide culture assays developed for Pseudomonas aeruginosa did not, however, exhibit this function.

Citing Articles

Whole genome sequence analysis of spp. isolated from ready-to-eat seafood: antimicrobial resistance and virulence factors.

Lee H, Storesund J, Lunestad B, Hoel S, Lerfall J, Jakobsen A Front Microbiol. 2023; 14:1175304.

PMID: 37455746 PMC: 10348363. DOI: 10.3389/fmicb.2023.1175304.


Comparative Genomics Revealed a Potential Threat of Aeromonas rivipollensis G87 Strain and Its Antibiotic Resistance.

Fono-Tamo E, Kamika I, Dewar J, Lekota K Antibiotics (Basel). 2023; 12(1).

PMID: 36671332 PMC: 9855013. DOI: 10.3390/antibiotics12010131.


Comparative and Evolutionary Genomics of Isolates Provide Insight into the Pathoadaptation of Aeromonas.

Talagrand-Reboul E, Colston S, Graf J, Lamy B, Jumas-Bilak E Genome Biol Evol. 2020; 12(5):535-552.

PMID: 32196086 PMC: 7250499. DOI: 10.1093/gbe/evaa055.


The Social Life of through Biofilm and Quorum Sensing Systems.

Talagrand-Reboul E, Jumas-Bilak E, Lamy B Front Microbiol. 2017; 8:37.

PMID: 28163702 PMC: 5247445. DOI: 10.3389/fmicb.2017.00037.


Interaction of Aeromonas strains with lactic acid bacteria via Caco-2 cells.

Hatje E, Neuman C, Katouli M Appl Environ Microbiol. 2013; 80(2):681-6.

PMID: 24242240 PMC: 3911096. DOI: 10.1128/AEM.03200-13.


References
1.
Janda J . Recent advances in the study of the taxonomy, pathogenicity, and infectious syndromes associated with the genus Aeromonas. Clin Microbiol Rev. 1991; 4(4):397-410. PMC: 358208. DOI: 10.1128/CMR.4.4.397. View

2.
Kirov S, Sanderson K, Dickson T . Characterisation of a type IV pilus produced by Aeromonas caviae. J Med Microbiol. 1999; 47(6):527-31. DOI: 10.1099/00222615-47-6-527. View

3.
Martinetti Lucchini G, Altwegg M . rRNA gene restriction patterns as taxonomic tools for the genus Aeromonas. Int J Syst Bacteriol. 1992; 42(3):384-9. DOI: 10.1099/00207713-42-3-384. View

4.
Iwanaga M, Hokama A . Characterization of Aeromonas sobria TAP13 pili: a possible new colonization factor. J Gen Microbiol. 1992; 138(9):1913-9. DOI: 10.1099/00221287-138-9-1913. View

5.
Ho A, Sohel I, Schoolnik G . Cloning and characterization of fxp, the flexible pilin gene of Aeromonas hydrophila. Mol Microbiol. 1992; 6(18):2725-32. DOI: 10.1111/j.1365-2958.1992.tb01449.x. View