A novel conjugative plasmid from Enterococcus faecalis E99 enhances resistance to ultraviolet radiation

被引:15
作者
Coburn, Phillip S. [1 ]
Baghdayan, Arto S. [1 ]
Craig, Nikki [1 ]
Burroughs, Adam [4 ]
Tendolkar, Preeti [1 ]
Miller, Kris [4 ]
Najar, Fares Z. [2 ,3 ]
Roe, Bruce A. [2 ,3 ]
Shankar, Nathan [1 ]
机构
[1] Univ Oklahoma, Hlth Sci Ctr, Dept Pharmaceut Sci, Oklahoma City, OK 73126 USA
[2] Univ Oklahoma, Dept Chem & Biochem, Norman, OK 73019 USA
[3] Univ Oklahoma, Adv Ctr Genome Technol, Norman, OK 73019 USA
[4] Oklahoma Christian Univ, Dept Biol, Oklahoma City, OK 73136 USA
关键词
Enterococcus faecalis; bee locus; pBEE99; Bacteriocin; Ultraviolet radiation resistance; Conjugation; STREPTOCOCCUS-FAECALIS; NUCLEOTIDE-SEQUENCE; PHEROMONE RESPONSE; GENETIC ANALYSES; SEX-PHEROMONE; PAD1; DNA; IDENTIFICATION; MUTAGENESIS; PHENOTYPE;
D O I
10.1016/j.plasmid.2010.03.001
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Enterococcus faecalis has emerged as a prominent healthcare-associated pathogen frequently encountered in bacteremia, endocarditis, urinary tract infection, and as a leading cause of antibiotic-resistant infections. We recently demonstrated a capacity for high-level biofilm formation by a clinical E. faecalis isolate, E99. This high biofilm-forming phenotype was attributable to a novel locus, designated bee, specifying a pilus at the bacterial cell surface and localized to a large similar to 80 kb conjugative plasmid. To better understand the origin of the bee locus, as well as to potentially identify additional factors important to the biology and pathogenesis of strain E99, we sequenced the entire plasmid. The nucleotide sequence of the plasmid, designated pBEE99, revealed large regions of identity to the previously characterized conjugative plasmid pCF10. In addition to the bee locus, pBEE99 possesses an open reading frame potentially encoding aggregation substance, as well as open reading frames putatively encoding polypeptides with 60% to 99% identity at the amino acid level to proteins involved in regulation of the pheromone response and conjugal transfer of pCF10. However, strain E99 did not respond to the cCF10 pheromone in clumping assays. While pBEE99 was found to be devoid of any readily recognizable antibiotic resistance determinants, it carries two non-identical impB/mucB/samB-type genes, as well as genes potentially encoding a two-component bacteriocin similar to that encoded on pYI14. Although no bacteriocin activity was detected from an OG1RF transconjugant carrying pBEE99 against strain FA2-2, it was approximately an order of magnitude more resistant to ultraviolet radiation. Moreover, curing strain E99 of this plasmid significantly reduced its ability to survive UV exposure. Therefore, pBEE99 represents a novel conjugative plasmid that confers biofilm-forming and enhanced UV resistance traits that might potentially impact the virulence and/or fitness of E. faecalis. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:18 / 25
页数:8
相关论文
共 28 条
[1]  
Clewell DB, 2002, ENTEROCOCCI: PATHOGENESIS, MOLECULAR BIOLOGY, AND ANTIBIOTIC RESISTANCE, P265
[2]   CHARACTERIZATION OF 3 PLASMID DEOXYRIBONUCLEIC-ACID MOLECULES IN A STRAIN OF STREPTOCOCCUS-FAECALIS - IDENTIFICATION OF A PLASMID DETERMINING ERYTHROMYCIN RESISTANCE [J].
CLEWELL, DB ;
YAGI, Y ;
DUNNY, GM ;
SCHULTZ, SK .
JOURNAL OF BACTERIOLOGY, 1974, 117 (01) :283-289
[3]   Horizontal transfer of virulence genes encoded on the Enterococcus faecalis pathogenicity island [J].
Coburn, Phillip S. ;
Baghdayan, Arto S. ;
Dolan, G. T. ;
Shankar, Nathan .
MOLECULAR MICROBIOLOGY, 2007, 63 (02) :530-544
[4]   Enterococcus faecalis conjugative plasmid pAM373:: complete nucleotide sequence and genetic analyses of sex pheromone response [J].
De Boever, EH ;
Clewell, DB ;
Fraser, CM .
MOLECULAR MICROBIOLOGY, 2000, 37 (06) :1327-1341
[5]   DIRECT STIMULATION OF THE TRANSFER OF ANTIBIOTIC-RESISTANCE BY SEX-PHEROMONES IN STREPTOCOCCUS-FAECALIS [J].
DUNNY, G ;
FUNK, C ;
ADSIT, J .
PLASMID, 1981, 6 (03) :270-278
[6]   The peptide pheromone-inducible conjugation system of Enterococcus faecalis plasmid pCF10:: cell-cell signalling, gene transfer, complexity and evolution [J].
Dunny, Gary M. .
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 2007, 362 (1483) :1185-1193
[7]   INDUCED CELL-AGGREGATION AND MATING IN STREPTOCOCCUS-FAECALIS - EVIDENCE FOR A BACTERIAL SEX-PHEROMONE [J].
DUNNY, GM ;
BROWN, BL ;
CLEWELL, DB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1978, 75 (07) :3479-3483
[8]   Replication of Enterococcus faecalis pheromone-responding plasmid pAD1:: Location of the minimal replicon and oriV site and RepA involvement in initiation of replication [J].
Francia, MV ;
Fujimoto, S ;
Tille, P ;
Weaver, KE ;
Clewell, DB .
JOURNAL OF BACTERIOLOGY, 2004, 186 (15) :5003-5016
[9]   Completion of the nucleotide sequence of the Enterococcus faecalis conjugative virulence plasmid pAD1 and identification of a second transfer origin [J].
Francia, MV ;
Haas, W ;
Wirth, R ;
Samberger, E ;
Muscholl-Silberhorn, A ;
Gilmore, MS ;
Ike, Y ;
Weaver, KE ;
An, FY ;
Clewell, DB .
PLASMID, 2001, 46 (02) :117-127
[10]  
Gilmore MS, 2002, ENTEROCOCCI: PATHOGENESIS, MOLECULAR BIOLOGY, AND ANTIBIOTIC RESISTANCE, P301