Salb inactivation modulates culture supernatant exoproteins and affects autolysis and viability in Enterococcus faecalis OG1RF

Journal of Bacteriology

Volumn 194, Issue 14, 2012, Pages 3569-3578

  Shankar, Jayendra ^a   Walker, Rachel G ^a,b   Wilkinson, Mark C ^a   Ward, Deborah ^a   Horsburgh, Malcolm J ^a  

^a UNIVERSITY OF LIVERPOOL   (United Kingdom)

^b Society for General Microbiology   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

BACTERIAL PROTEIN; PEPTIDOGLYCAN; SALB PROTEIN; UNCLASSIFIED DRUG;

ARTICLE; AUTOLYSIS; BACTERIAL STRAIN; BACTERIAL VIABILITY; BACTERIUM CULTURE; CELL DIVISION; ENTEROCOCCUS FAECALIS; GEL ELECTROPHORESIS; GENE INACTIVATION; GENE MUTATION; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; MATRIX ASSISTED LASER DESORPTION IONIZATION TIME OF FLIGHT MASS SPECTROMETRY; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; PROTEIN ANALYSIS;

ANTIGENS, BACTERIAL; BACTERIAL PROTEINS; BACTERIOLYSIS; CLONING, MOLECULAR; ENTEROCOCCUS FAECALIS; GENE EXPRESSION REGULATION, BACTERIAL; MICROBIAL VIABILITY; MUTATION; PEPTIDOGLYCAN; PROTEOME; SPECTROMETRY, MASS, MATRIX-ASSISTED LASER DESORPTION-IONIZATION; STRESS, PHYSIOLOGICAL;

ENTEROCOCCUS FAECALIS;

EID: 84864004521     PISSN: 00219193     EISSN: 10985530     Source Type: Journal    
DOI: 10.1128/JB.00376-12     Document Type: Article

References (38)

1. Arias CA, Cortes L, Murray BE. 2007. Chaining in enterococci revisited: correlation between chain length and gelatinase phenotype, and gelE and fsrB genes among clinical isolates of Enterococcus faecalis. J. Med. Microbiol. 56:286 -288.
2. Barendt SM, et al. 2009. Influences of capsule on cell shape and chain formation of wild-type and pcsB mutants of serotype 2 Streptococcus pneumoniae. J. Bacteriol. 191:3024 -3040.
3. Biavasco F, et al. 1996. In vitro conjugative transfer of VanA vancomycin resistance between enterococci and listeriae of different species. Eur. J. Clin. Microbiol. Infect. Dis. 15:50 -59.
4. Bonten MJ, Willems R, Weinstein RA. 2001. Vancomycin-resistant enterococci: why are they here and where do they come from? Lancet Infect. Dis. 1:314 -325.
5. Breton YL, et al. 2002. Isolation and characterization of bile saltssensitive mutants of Enterococcus faecalis. Curr. Microbiol. 45:434-439.
6. Chaussee MA, McDowell EJ, Chaussee MS. 2008. Proteomic analysis of proteins secreted by Streptococcus pyogenes. Methods Mol. Biol. 431: 15-24.
7. Comenge Y, et al. 2003. The CroRS two-component regulatory system is required for intrinsic beta-lactam resistance in Enterococcus faecalis. J. Bacteriol. 185:7184 -7192.
8. Eckert C, Lecerf M, Dubost L, Arthur M, Mesnage S. 2006. Functional analysis of AtlA, the major N-acetylglucosaminidase of Enterococcus faecalis. J. Bacteriol. 188:8513- 8519.
9. Giefing-Kroll C, Jelencsics KE, Reipert S, Nagy E. 2011. Absence of pneumococcal PcsB is associated with overexpression of LysM domaincontaining proteins. Microbiology 157:1897-1909.
10. Gilmore MS, Ferretti JJ. 2003. The thin line between gut commensal and pathogen. Science 299:1999 -2002.
11. Hancock LE, Gilmore MS. 2006. Pathogenicity of enterococci, p 301-354. In Fischetti V, Novick R, Ferretti J, Portnoy D, Rood J (ed), Gram-positive organisms. ASM Press, Washington, DC.
12. Horsburgh MJ, Wiltshire MD, Crossley H, Ingham E, Foster SJ. 2004. PheP, a putative amino acid permease of Staphylococcus aureus, contributes to survival in vivo and during starvation. Infect. Immun. 72:3073- 3076.
13. Land AD, Winkler ME. 2011. The requirement for pneumococcal MreC and MreD is relieved by inactivation of the gene encoding PBP1a. J. Bacteriol. 193:4166-4179.
14. Le Breton Y, et al. 2003. Molecular characterization of Enterococcus faecalis two-component signal transduction pathways related to environmental stresses. Environ. Microbiol. 5:329 -337.
15. Mesnage S, Chau F, Dubost L, Arthur M. 2008. Role of Nacetylglucosaminidase and N-acetylmuramidase activities in Enterococcus faecalis peptidoglycan metabolism. J. Biol. Chem. 283:19845-19853.
16. Miller D, Urdaneta V, Weltman A. 2002. Public health dispatch: vancomycin-resistant Staphylococcus aureus-Pennsylvania. MMWR Morb. Mortal. Wkly. Rep. 51:902.
17. Mohamed JA, Teng F, Nallapareddy SR, Murray BE. 2006. Pleiotrophic effects of 2 Enterococcus faecalis sagA-like genes, salA and salB, which encode proteins that are antigenic during human infection, on biofilm formation and binding to collagen type I and fibronectin. J. Infect. Dis. 193: 231-240.
18. Muller C, et al. 2006. The response regulator CroR modulates expression of the secreted stress-induced SalB protein in Enterococcus faecalis. J. Bacteriol. 188:2636 -2645.
19. Nakayama J, Kariyama R, Kumon H. 2002. Description of a 23.9-kilobase chromosomal deletion containing a region encoding fsr genes which mainly determines the gelatinase-negative phenotype of clinical isolates of Enterococcus faecalis in urine. Appl. Environ. Microbiol. 68: 3152-3155.
20. Paulsen IT, et al. 2003. Role of mobile DNA in the evolution of vancomycin-resistant Enterococcus faecalis. Science 299:2071-2074.
21. Qin X, Singh KV, Weinstock GM, Murray BE. 2001. Characterization of fsr, a regulator controlling expression of gelatinase and serine protease in Enterococcus faecalis OG1RF. J. Bacteriol. 183:3372-3382.
22. Ramirez-Arcos S, Liao M, Marthaler S, Rigden M, Dillon JA. 2005. Enterococcus faecalis divIVA: an essential gene involved in cell division, cell growth and chromosome segregation. Microbiology 151:1381- 1393.
23. Reinscheid DJ, Ehlert K, Chhatwal GS, Eikmanns BJ. 2003. Functional analysis of a PcsB-deficient mutant of group B Streptococcus. FEMS Microbiol. Lett. 221:73-79.
24. Reinscheid DJ, Gottschalk B, Schubert A, Eikmanns BJ, Chhatwal GS. 2001. Identification and molecular analysis of PcsB, a protein required for cell wall separation of group B Streptococcus. J. Bacteriol. 183:1175-1183.
25. Rince A, et al. 2003. Physiological and molecular aspects of bile salt response in Enterococcus faecalis. Int. J. Food Microbiol. 88:207-213.
26. Rosenthal RS, Dziarski R. 1994. Isolation of peptidoglycan and soluble peptidoglycan fragments. Methods Enzymol. 235:253-285.
27. Seno Y, Kariyama R, Mitsuhata R, Monden K, Kumon H. 2005. Clinical implications of biofilm formation by Enterococcus faecalis in the urinary tract. Acta Med. Okayama 59:79-87.
28. Sham LT, Barendt SM, Kopecky KE, Winkler ME. 2011. Essential PcsB putative peptidoglycan hydrolase interacts with the essential FtsXSpn cell division protein in Streptococcus pneumoniae D39. Proc. Natl. Acad. Sci. U. S. A. 108:E1061-E1069.
29. Shankar J, Walker RG, Ward D, Horsburgh MJ. 2012. The Enterococcus faecalis exoproteome: identification and temporal regulation by Fsr. PLoS One 7:e33450. doi:10.1371/journal.pone.0033450.
30. Sievert D, et al. 2002. Staphylococcus aureus resistant to vancomycin- United States. MMWR Morb. Mortal. Wkly. Rep. 51:565-567.
31. Singh KV, Qin X, Weinstock GM, Murray BE. 1998. Generation and testing of mutants of Enterococcus faecalis in a mouse peritonitis model. J. Infect. Dis. 178:1416 -1420.
32. Smith TJ, Foster SJ. 1995. Characterization of the involvement of two compensatory autolysins in mother cell lysis during sporulation of Bacillus subtilis 168. J. Bacteriol. 177:3855-3862.
33. Tendolkar P, Baghdayan A, Shankar N. 2003. Pathogenic entero-cocci: new developments in the 21st century. Cell. Mol. Life Sci. 60: 2622-2636.
34. Teng F, Kawalec M, Weinstock GM, Hryniewicz W, Murray BE. 2003. An Enterococcus faecium secreted antigen, SagA, exhibits broad-spectrum binding to extracellular matrix proteins and appears essential for E. faecium growth. Infect. Immun. 71:5033-5041.
35. Thomas VC, et al. 2009. A fratricidal mechanism is responsible for eDNA release and contributes to biofilm development of Enterococcus faecalis. Mol. Microbiol. 72:1022-1036.
36. Trieu-Cuot P, Carlier C, Poyart-Salmeron C, Courvalin P. 1991. Shuttle vectors containing a multiple cloning site and a lacZ alpha gene for conjugal transfer of DNA from Escherichia coli to Gram-positive bacteria. Gene 102:99 -104.
37. Waters CM, Antiporta MH, Murray BE, Dunny GM. 2003. Role of the Enterococcus faecalis GelE protease in determination of cellular chain length, supernatant pheromone levels, and degradation of fibrin and misfolded surface proteins. J. Bacteriol. 185:3613-3623.
38. Yasmin A, et al. 2010. Comparative genomics and transduction potential of Enterococcus faecalis temperate bacteriophages. J. Bacteriol. 192:1122- 1130.