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New Insights into the Enterococcus faecium and Streptococcus gallolyticus subsp. gallolyticus Host Interaction Mechanisms.

Title: New Insights into the Enterococcus faecium and Streptococcus gallolyticus subsp. gallolyticus Host Interaction Mechanisms.
Authors: Sánchez-Díaz AM; Servicio de Microbiología, Hospital Universitario Ramón y Cajal and Instituto Ramón y Cajal de Investigación Sanitaria (IRYCIS), Madrid, Spain.; Red Española de Investigación en Patología Infecciosa (REIPI), Sevilla, Spain.; Romero-Hernández B; Servicio de Microbiología, Hospital Universitario Ramón y Cajal and Instituto Ramón y Cajal de Investigación Sanitaria (IRYCIS), Madrid, Spain.; Conde-Moreno E; Grupo de Biomarcadores y Dianas Terapéuticas, Hospital Universitario Ramón y Cajal and IRYCIS, Madrid, Spain.; Kwak YK; Microbiology Tumor and Cell Biology Department (MTC), Karolinska Institutet, Stockholm, Sweden.; Zamora J; Unidad de Bioestadística Clínica, Hospital Universitario Ramón y Cajal and IRYCIS, Madrid, Spain.; Colque-Navarro P; Microbiology Tumor and Cell Biology Department (MTC), Karolinska Institutet, Stockholm, Sweden.; Möllby R; Microbiology Tumor and Cell Biology Department (MTC), Karolinska Institutet, Stockholm, Sweden.; Ruiz-Garbajosa P; Servicio de Microbiología, Hospital Universitario Ramón y Cajal and Instituto Ramón y Cajal de Investigación Sanitaria (IRYCIS), Madrid, Spain.; Red Española de Investigación en Patología Infecciosa (REIPI), Sevilla, Spain.; Cantón R; Servicio de Microbiología, Hospital Universitario Ramón y Cajal and Instituto Ramón y Cajal de Investigación Sanitaria (IRYCIS), Madrid, Spain.; Red Española de Investigación en Patología Infecciosa (REIPI), Sevilla, Spain.; García-Bermejo L; Grupo de Biomarcadores y Dianas Terapéuticas, Hospital Universitario Ramón y Cajal and IRYCIS, Madrid, Spain.; Del Campo R; Servicio de Microbiología, Hospital Universitario Ramón y Cajal and Instituto Ramón y Cajal de Investigación Sanitaria (IRYCIS), Madrid, Spain.; Red Española de Investigación en Patología Infecciosa (REIPI), Sevilla, Spain.
Source: PloS one [PLoS One] 2016 Jul 27; Vol. 11 (7), pp. e0159159. Date of Electronic Publication: 2016 Jul 27 (Print Publication: 2016).
Publication Type: Journal Article
Language: English
Journal Info: Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: eCollection Cited Medium: Internet ISSN: 1932-6203 (Electronic) Linking ISSN: 19326203 NLM ISO Abbreviation: PLoS One Subsets: MEDLINE
Imprint Name(s): Original Publication: San Francisco, CA : Public Library of Science
MeSH Terms: Host-Pathogen Interactions*; Enterococcus faecium/*physiology ; Streptococcus gallolyticus/*physiology; Biofilms ; Caco-2 Cells ; Humans
Abstract: Enterococcus faecium and Streptococcus gallolyticus subsp. gallolyticus (S. gallolyticus) were classically clustered into the Lancefield Group D streptococci and despite their taxonomic reclassification still share a similar genetic content and environment. Both species are considered as opportunistic pathogens. E. faecium is often associated with nosocomial bacteraemia, and S. gallolyticus is sporadically found in endocarditis of colorectal cancer patients. In both cases, the source of infection is commonly endogenous with a translocation process that launches through the intestinal barrier. To get new insights into the pathological processes preceding infection development of both organisms, we used an in vitro model with Caco-2 cells to study and compare the adhesion, invasion and translocation inherent abilities of 6 E. faecium and 4 S. gallolyticus well-characterized isolates. Additionally, biofilm formation on polystyrene, collagen I and IV was also explored. Overall results showed that E. faecium translocated more efficiently than S. gallolyticus, inducing a destabilization of the intestinal monolayer. Isolates Efm106, Efm121 and Efm113 (p < .001 compared to Ef222) exhibited the higher translocation ability and were able to adhere 2-3 times higher than S. gallolyticus isolates. Both species preferred the collagen IV coated surfaces to form biofilm but the S. gallolyticus structures were more compact (p = .01). These results may support a relationship between biofilm formation and vegetation establishment in S. gallolyticus endocarditis, whereas the high translocation ability of E. faecium high-risk clones might partially explain the increasing number of bacteraemia.
References: J Clin Microbiol. 2011 Sep;49(9):3228-33. (PMID: 21752968); Lancet Infect Dis. 2013 Aug;13(8):719-24. (PMID: 23831427); Diagn Microbiol Infect Dis. 2004 Sep;50(1):59-69. (PMID: 15380279); J Clin Pathol. 1978 Dec;31(12):1182-6. (PMID: 107199); BMC Microbiol. 2010 Mar 16;10:78. (PMID: 20233397); J Clin Invest. 2010 Dec;120(12):4332-41. (PMID: 21099116); PLoS One. 2015 May 15;10(5):e0126507. (PMID: 25978355); Int J Cancer. 2016 Apr 1;138(7):1670-9. (PMID: 26537841); FEMS Microbiol Lett. 2014 Apr;353(2):151-6. (PMID: 24606170); Am J Physiol Gastrointest Liver Physiol. 2010 Jun;298(6):G851-9. (PMID: 20224007); Am J Physiol. 1984 Sep;247(3 Pt 1):C260-7. (PMID: 6476109); FEMS Immunol Med Microbiol. 2008 Apr;52(3):297-308. (PMID: 18279340); Infect Genet Evol. 2015 Jul;33:419-36. (PMID: 25233845); J Med Microbiol. 2007 Dec;56(Pt 12):1581-8. (PMID: 18033823); Clin Infect Dis. 2011 Nov;53(9):870-8. (PMID: 21960713); Eur J Clin Microbiol Infect Dis. 2012 Apr;31(4):519-22. (PMID: 21789603); Int J Med Microbiol. 2011 Mar;301(3):240-51. (PMID: 21112248); Clin Infect Dis. 2012 Oct;55(7):905-14. (PMID: 22718773); PLoS One. 2014 Sep 25;9(9):e108453. (PMID: 25255079); Clin Microbiol Infect. 2007 Mar;13(3):316-9. (PMID: 17391388); Future Microbiol. 2009 Nov;4(9):1125-35. (PMID: 19895216); Acta Medica (Hradec Kralove). 2011;54(1):3-8. (PMID: 21542416); Med Microbiol Immunol. 2001 Dec;190(3):113-20. (PMID: 11827199); PLoS One. 2013 Sep 19;8(9):e74734. (PMID: 24069339); Appl Environ Microbiol. 2015 Mar;81(5):1820-31. (PMID: 25548052); J Infect Dis. 2011 Dec 15;204(12):1960-70. (PMID: 22043018); Clin Microbiol Infect. 2014 Feb;20(2):145-51. (PMID: 23647880); J Bacteriol. 2007 Nov;189(22):8233-40. (PMID: 17827282); J Lab Autom. 2015 Apr;20(2):107-26. (PMID: 25586998); J Bacteriol. 2009 Nov;191(21):6643-53. (PMID: 19717590); Antimicrob Agents Chemother. 2015 Apr;59(4):2006-15. (PMID: 25605355); PLoS Pathog. 2010 May 27;6(5):e1000879. (PMID: 20523891); Clin Microbiol Infect. 2016 Jan;22(1):59.e1-8. (PMID: 26321668); BMC Infect Dis. 2012 Mar 22;12:68. (PMID: 22436212); J Infect Dis. 2011 Apr 15;203(8):1101-9. (PMID: 21451000); J Clin Microbiol. 2009 Apr;47(4):896-901. (PMID: 19193843); J Gastroenterol Hepatol. 2007 Apr;22(4):464-71. (PMID: 17376034); Gut. 2003 Jul;52(7):988-97. (PMID: 12801956)
Entry Date(s): Date Created: 20160728 Date Completed: 20170717 Latest Revision: 20181113
Update Code: 20260130
PubMed Central ID: PMC4963119
DOI: 10.1371/journal.pone.0159159
PMID: 27463203
Database: MEDLINE

Journal Article