Bacteriocin production in vancomycin-resistant and vancomycin-susceptible Enterococcus isolates of different origins

被引:66
作者
del Campo, R
Tenorio, C
Jiménez-Díaz, R
Rubio, C
Gómez-Lus, R
Baquero, F
Torres, C
机构
[1] Univ La Rioja, Area Bioquim & Biol Mol, Logrono 26006, Spain
[2] CSIC, Inst Grasa, Dept Biotecnol Alimentos, Seville, Spain
[3] Univ Zaragoza, Dept Microbiol, Zaragoza, Spain
[4] Hosp Ramon y Cajal, Microbiol Serv, E-28034 Madrid, Spain
关键词
D O I
10.1128/AAC.45.3.905-912.2001
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Bacteriocin production was determined for 218 Enierococcus isolates (Enterococcus faecalis [93] and E, faecium [125]) obtained from different origins (human clinical samples [87], human fecal samples [78], sewage [28], and chicken samples [25]) and showing different vancomycin susceptibility patterns (vancomycin resistant, all of them vanA positive [56], and vancomycin susceptible [162]), All enterococcal isolates were randomly selected except for the vancomycin-resistant ones. A total of 33 isolates of eight different bacterial genera were used as indicators for bacteriocin production. Forty-seven percent of the analyzed enterococcal isolates were bacteriocin producers (80.6% of E. faecalis and 21,6% of E, faecium isolates). The percentage of bacteriocin producers was higher among human clinical isolates (63.2%, 81.8% of vancomycin-resistant isolates and 60.5% of vancomycin-susceptible ones) than among isolates from the other origins (28 to 39.3%). Only one out of the 15 vancomycin-resistant isolates from human fecal samples was a bacteriocin producer, while 44.4% of fecal vancomycin-susceptible isolates were, The bacteriocin produced by the vanA-containing E, faecium strain RC714, named bacteriocin RC714, was further characterized. This bacteriocin activity was cotransferred together with the vanA genetic determinant to E,faecalis strain JH2-2. Bacteriocin RC714 was purified to homogeneity and its primary structure was determined by amino acid sequencing, showing an identity of 88% and a similarity of 92% with the previously described bacteriocin 31 from E, faecalis YI717, The presence of five different amino acids in bacteriocin RC714 suggest that this could be a new bacteriocin. The results obtained suggest that the epidemiology of vancomycin resistance may be influenced by different factors, including bacteriocin production.
引用
收藏
页码:905 / 912
页数:8
相关论文
共 60 条
[1]   Occurrence of glycopeptide resistance among Enterococcus faecium isolates from conventional and ecological poultry farms [J].
Aarestrup, FM .
MICROBIAL DRUG RESISTANCE-MECHANISMS EPIDEMIOLOGY AND DISEASE, 1995, 1 (03) :255-257
[2]  
AMERICH T, 1996, APPL ENVIRON MICROB, V62, P1676
[3]   CHARACTERIZATION OF THE DETERMINANT (TRAB) ENCODING SEX-PHEROMONE SHUTDOWN BY THE HEMOLYSIN BACTERIOCIN PLASMID-PAD1 IN ENTEROCOCCUS-FAECALIS [J].
AN, FY ;
CLEWELL, DB .
PLASMID, 1994, 31 (02) :215-221
[4]   BACTERIOCIN (HEMOLYSIN) OF STREPTOCOCCUS ZYMOGENES [J].
BASINGER, SF ;
JACKSON, RW .
JOURNAL OF BACTERIOLOGY, 1968, 96 (06) :1895-&
[5]   FARM-ANIMALS AS A PUTATIVE RESERVOIR FOR VANCOMYCIN-RESISTANT ENTEROCOCCAL INFECTION IN MAN [J].
BATES, J ;
JORDENS, JZ ;
GRIFFITHS, DT .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1994, 34 (04) :507-514
[6]   DIRECT DETECTION OF AN ANTIMICROBIAL PEPTIDE OF PEDIOCOCCUS-ACIDILACTICI IN SODIUM DODECYL SULFATE-POLYACRYLAMIDE GEL-ELECTROPHORESIS [J].
BHUNIA, AK ;
JOHNSON, MC ;
RAY, B .
JOURNAL OF INDUSTRIAL MICROBIOLOGY, 1987, 2 (05) :319-322
[7]  
BROCK DT, 1963, J BACTERIOL, V86, P708
[8]   Enterococci with acquired vancomycin resistance in pigs and chickens of different age groups [J].
Butaye, P ;
Devriese, LA ;
Goossens, H ;
Ieven, M ;
Haesebrouck, F .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1999, 43 (02) :365-366
[9]   Enterocin B, a new bacteriocin from Enterococcus faecium T136 which can act synergistically with enterocin A [J].
Casaus, P ;
Nilsen, T ;
Cintas, LM ;
Nes, IF ;
Hernandez, PE ;
Holo, H .
MICROBIOLOGY-SGM, 1997, 143 :2287-2294
[10]   PLASMID-ASSOCIATED HEMOLYSIN AND AGGREGATION SUBSTANCE PRODUCTION CONTRIBUTE TO VIRULENCE IN EXPERIMENTAL ENTEROCOCCAL ENDOCARDITIS [J].
CHOW, JW ;
THAL, LA ;
PERRI, MB ;
VAZQUEZ, JA ;
DONABEDIAN, SM ;
CLEWELL, DB ;
ZERVOS, MJ .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1993, 37 (11) :2474-2477