Production of antilisterial bacteriocins by staphylococci isolated from bovine milk

Journal of Dairy Science

Volumn 94, Issue 3, 2011, Pages 1194-1200

  Brito, M A V P ^a   Somkuti, G A ^b   Renye, J A ^b  

^a EMBRAPA CERRADOS   (Brazil)

^b EASTERN REGIONAL RESEARCH CENTER   (United States)

Author keywords

Antilisterial activity; Bacteriocin; Staphylococci from milk

Indexed keywords

ANTIINFECTIVE AGENT; BACTERIOCIN;

ANIMAL; ARTICLE; BIOSYNTHESIS; CATTLE; GENETICS; GROWTH, DEVELOPMENT AND AGING; ISOLATION AND PURIFICATION; LISTERIA MONOCYTOGENES; METABOLISM; MICROBIOLOGY; MILK; STAPHYLOCOCCUS; STAPHYLOCOCCUS AUREUS;

ANIMALS; ANTI-BACTERIAL AGENTS; BACTERIOCINS; CATTLE; LISTERIA MONOCYTOGENES; MILK; STAPHYLOCOCCUS; STAPHYLOCOCCUS AUREUS;

BACTERIA (MICROORGANISMS); BOVINAE; LISTERIA MONOCYTOGENES; STAPHYLOCOCCUS;

EID: 79951700107     PISSN: 00220302     EISSN: 15253198     Source Type: Journal    
DOI: 10.3168/jds.2010-3849     Document Type: Article

References (48)

1. Augustin J., Gotz F. Transformation of Staphylococcus epidermidis and other staphylococcal species with plasmid DNA by electroporation. FEMS Microbiol. Lett. 1990, 54:203-207.
2. Barrow G.I. The nature of inhibitory activity by Staphylococcus aureus Type 71. J. Gen. Microbiol. 1963, 32:255-261.
3. Chen H., Hoover D.G. Bacteriocins and their food applications. Comp. Rev. Food Sci. Food Safety 2003, 2:82-100.
4. Cottrell M.T., Kirchman D.L. Community of marine bacterioplankton determined by 16S rRNA gene clone libraries and fluorescence in situ hybridization. Appl. Environ. Microbiol. 2000, 66:5116-5122.
5. Crupper S.S., Gies A.J., Iandolo J.J. Purification and characterization of staphylococcin BacR1, a broad-spectrum bacteriocin. Appl. Environ. Microbiol. 1997, 63:4185-4190.
6. Crupper S.S., Iandolo J.J. Purification and partial characterization of a novel antibacterial agent (Bac1829) produced by Staphylococcus aureus KSI1829. Appl. Environ. Microbiol. 1996, 62:3171-3175.
7. Dajani A.S., Wannamaker L.W. Demonstration of a bactericidal substance against β-hemolytic streptococci in supernatant fluids of staphylococcal cultures. J. Bacteriol. 1969, 97:985-991.
8. Deegan L., Cotter P.D., Hill C., Ross P. Bacteriocins: Biological tools for bio-preservation and shelf-life extension. Int. Dairy J. 2006, 16:1058-1071.
9. Ekkelenkamp M.B., Hanssen M., Hsu S.D., de Jong A., Milatovic D., Verhoef J., Van Nuland N.A.J. Isolation and structural characterization of epilancin 15X, a novel lantibiotic from a clinical strain of Staphylococcus epidermidis. FEBS Lett. 2005, 579:1917-1922.
10. Gagliano V.J., Hinsdill R.D. Characterization of a Staphylococcus aureus bacteriocin. J. Bacteriol. 1970, 104:117-125.
11. Giambiagi-Marval M., Mafra M.A., Penido E.G.C., Bastos M.C.F. Distinct groups of plasmids correlated with bacteriocin production in Staphylococcus aureus. J. Gen. Microbiol. 1990, 136:1591-1599.
12. Gotz F. Staphylococcus carnosus: A new host organism for gene cloning and protein production. Soc. Appl. Bacteriol. Symp. Ser. 1990, 19:49S-53S.
13. Guidry A., Fattom A., Patel A., O'Brien C., Shepard S., Lohuis J. Serotyping scheme for Staphylococcus aureus isolated from cows with mastitis. Am. J. Vet. Res. 1998, 59:1537-1539.
14. Hammes W.P., Bosch I., Wolf G. Contribution of Staphylococcus carnosus and Staphylococcus piscifermentans to the fermentation of protein foods. J. Appl. Bacteriol. 1995, 79(Symp. Suppl.):76-83.
15. Heidrich C., Pag U., Josten M., Metzger J., Jack R.W., Bierbaum G., Jung G., Sahl H.G. Isolation, characterization, and heterologous expression of the novel lantibiotic epicidin 280 and analysis of its biosynthetic gene cluster. Appl. Environ. Microbiol. 1998, 64:3140-3146.
16. Henderson J.T., Chopko A.L., Wassenaar P.D. Purification and primary structure of pediocin PA-1 produced by Pediococcus acidilactici. Arch. Biochem. Biophys. 1992, 295:5-12.
17. Jack R.W., Tagg J.R., Ray B. Bacteriocins of gram-positive bacteria. Microbiol. Rev. 1995, 59:171-200.
18. Lee J.C. Electroporation of staphylococci. Methods Mol. Biol. 1995, 47:209-216.
19. Leroy F., Verluyten J., De Vuyst L. Functional meat starter cultures for improved sausage fermentation. Int. J. Food Microbiol. 2006, 106:270-285.
20. Minamikawa M., Kawai Y., Inoue N., Yamazaki K. Purification and characterization of warnericin RB4, anti-Alicyclobacillus bacteriocin, produced by Staphylococcus warneri RB4. Curr. Microbiol. 2005, 51:22-26.
21. Nascimento J.S., Fagundes P.C., Brito M.A.V.P., Santos K.R.N., Bastos M.C.F. Production of bacteriocins by coagulase-negative staphylococci involved in bovine mastitis. Vet. Microbiol. 2005, 106:61-71.
22. Nascimento J.S., Giambiagi-Marval M., Oliveira S.S., Ceotto H., Santos K.R.N., Bastos M.C.F. Genomic fingerprinting of bacteriocin-producer strains of Staphylococcus aureus. Res. Microbiol. 2005, 156:837-842.
23. Nascimento J.S., Santos K.R.N., Gentilini E., Sordelli D., Bastos M.C.F. Phenotypic and genetic characterisation of bacteriocin-producing strains of Staphylococcus aureus involved in bovine mastitis. Vet. Microbiol. 2002, 85:133-144.
24. Navaratna M.A.D.B., Sahl H.G., Tagg J.R. Two-component anti-Staphylococcus aureus lantibiotic activity produced by Staphylococcus aureus C55. Appl. Environ. Microbiol. 1998, 64:4803-4808.
25. Navaratna M.A.D.B., Sahl H.G., Tagg J.R. Identification of genes encoding two-component lantibiotic production in Staphylococcus aureus C55 and other phage group II S. aureus strains and demonstration of an association with exfoliative toxin B gene. Infect. Immun. 1999, 67:4268-4271.
26. Netz D.J.A., Pohl R., Beck-Sickinger A.G., Selmer T., Pierik A.J., Bastos M.C.F., Sahl H.G. Biochemical characterisation and genetic analysis of aureocin A53, a new atypical bacteriocin from Staphylococcus aureus. J. Mol. Biol. 2002, 319:745-756.
27. Netz D.J.A., Sahl H.G., Marcelino R., Nascimento R.J.S., Oliveira S.S., Soares M.B., Bastos M.C.F. Molecular characterisation of aureocin A70, a multipeptide bacteriocin isolated from Staphylococcus aureus. J. Mol. Biol. 2001, 311:939-949.
28. O'Sullivan D., Klaenhammer T.R. Rapid mini-prep isolation of high-quality plasmid DNA from Lactococcus and Lactobacillus spp. Appl. Environ. Microbiol. 1993, 59:2730-2733.
29. O'Sullivan L., Ross R.P., Hill C. Potential of bacteriocin-producing lactic acid bacteria for improvements in food safety and quality. Biochimie 2002, 84:593-604.
30. Oliveira S.S., Nascimento J.S., Povoa D.C., Araujo S.A., Gamon M.R., Bastos A.C.F. Genetic analysis of the bacteriocin-encoding plasmids pRJ6 and pRJ9 of Staphylococcus aureus by transposon mutagenesis and cloning of genes involved in bacteriocin production. J. Appl. Microbiol. 1998, 85:972-984.
31. Papagianni M. Ribosomally synthesized peptides with antimicrobial properties: Biosynthesis, structure, function, and applications. Biotechnol. Adv. 2003, 21:465-499.
32. Rogolsky M., Wiley B.B. Production and properties of a staphylococcin genetically controlled by staphylococcal plasmid for exfoliative toxin synthesis. Infect. Immun. 1977, 15:726-732.
33. Sahl H.G., Bierbaum G. Lantibiotics: Biosynthesis and biological activities of uniquely modified peptides from gram-positive bacteria. Annu. Rev. Microbiol. 1998, 52:41-79.
34. Sahl H.G., Brandis H. Production, purification and chemical properties of an antistaphylococcal agent produced by Staphylococcus epidermidis. J. Gen. Microbiol. 1981, 127:377-384.
35. Sashihara T., Kimura H., Higuchi T., Adachi A., Matsusaki H., Sonomoto K., Ishizaki A.A. A novel lantibiotic nukacin ISK-1 of Staphylococcus warneri ISK-1: Cloning of the structural gene and identification of the structure. Biosci. Biotechnol. Biochem. 2000, 64:2420-2428.
36. Schenk S., Laddaga R.A. Improved method for electroporation of Staphylococcus aureus. FEMS Microbiol. Lett. 1992, 73:133-138.
37. Schleifer K., Fischer K.H. Description of a new species of the genus Staphylococcus: Staphylococcus carnosus. Int. J. Syst. Bacteriol. 1982, 32:153-156.
38. Schnell N., Engelke G., Augustin J., Rosenstein R., Ungerman V., Gotz F., Entian K.D. Analysis of genes involved in the biosynthesis of lantibiotic epidermin. Eur. J. Biochem. 1992, 204:57-68.
39. Schnell N., Entian K.D., Götz F., Horner T., Kellner R., Jung G. Structural gene isolation and prepeptide sequence of gallidermin, a new lanthionine containing antibiotic. FEMS Microbiol. Lett. 1989, 49:263-267.
40. Siezen R.J., Kuipers O.P., de Vos W.M. Comparison of lantibiotic gene clusters and encoded proteins. Antonie van Leeuwenhoek 1996, 69:174-184.
41. Somkuti G.A., Steinberg D.H. Genetic transformation of Streptococcus thermophilus by electroporation. Biochimie 1988, 70:579-585.
42. Stougaard P., Molin S. Vertical dye-buoyant density gradients for rapid analysis and preparation of plasmid DNA. Anal. Biochem. 1983, 118:191-193.
43. Sutra L., Poutrel B. Virulence factors involved in the pathogenesis of bovine intramammary infections due to Staphylococcus aureus. J. Med. Microbiol. 1994, 40:79-89.
44. Tagg J.R., McGiven A.R. Assay system for bacteriocins. Appl. Microbiol. 1971, 21:943.
45. van de Kamp M., Horstink L.M., Van den Hooven H.W., Konings R.N.H., Hilbers C.W., Frey A., Sahl H.G., Metzger J.W., Van de Ven F.J.M. Sequence analysis by NMR spectroscopy of the peptide lantibiotic epilancin K7 from Staphylococcus epidermidis K7. Eur. J. Biochem. 1995, 227:757-771.
46. Wall R.J., Powell A.M., Paape M.J., Kerr D.E., Bannerman D.D., Pursel V.G., Wells K.D., Talbot N., Hawk H.W. Genetically enhanced cows resist intramammary Staphylococcus aureus infection. Nat. Biotechnol. 2005, 23:445-451.
47. Warren R., Rogolsky M., Wiley B.B., Glasgow L.A. Isolation of extrachromosomal deoxyribonucleic acid for exfoliative toxin production from phage group II Staphylococcus aureus. J. Bacteriol. 1975, 122:99-105.
48. Wernérus H., Lehtiö J., Samuelson P., Stahl S. Engineering of staphylococcal surfaces for biotechnological applications. J. Biotechnol. 2002, 96:67-78.