Identification of bacterial plasmids based on mobility and plasmid population biology

被引:121
作者
Pilar Garcillan-Barcia, Maria
Alvarado, Andres
de la Cruz, Fernando [1 ]
机构
[1] Univ Cantabria, CSIC, IDICAN, Dept Biol Mol, C Herrera Oria S-N, Santander 39011, Spain
关键词
plasmid classification; plasmid conjugation; antibiotic resistance; relaxase; plasmid population genetics; plasmid replication; COMPLETE NUCLEOTIDE-SEQUENCE; SPECTRUM-BETA-LACTAMASE; DNA RESTRICTION SYSTEMS; ESCHERICHIA-COLI STRAIN; ANTIBIOTIC-RESISTANCE; KLEBSIELLA-PNEUMONIAE; CONJUGATIVE PLASMID; DRUG-RESISTANCE; ANTIMICROBIAL RESISTANCE; QUINOLONE RESISTANCE;
D O I
10.1111/j.1574-6976.2011.00291.x
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Plasmids contain a backbone of core genes that remains relatively stable for long evolutionary periods, making sense to speak about plasmid species. The identification and characterization of the core genes of a plasmid species has a special relevance in the study of its epidemiology and modes of transmission. Besides, this knowledge will help to unveil the main routes that genes, for example antibiotic resistance (AbR) genes, use to travel from environmental reservoirs to human pathogens. Global dissemination of multiple antibiotic resistances and virulence traits by plasmids is an increasing threat for the treatment of many bacterial infectious diseases. To follow the dissemination of virulence and AbR genes, we need to identify the causative plasmids and follow their path from reservoirs to pathogens. In this review, we discuss how the existing diversity in plasmid genetic structures gives rise to a large diversity in propagation strategies. We would like to propose that, using an identification methodology based on plasmid mobility types, we can follow the propagation routes of most plasmids in Gammaproteobacteria, as well as their cargo genes, in complex ecosystems. Once the dissemination routes are known, designing antidissemination drugs and testing their efficacy will become feasible.
引用
收藏
页码:936 / 956
页数:21
相关论文
共 147 条
[1]   Dissemination of blaKPC-2 by the Spread of Klebsiella pneumoniae Clonal Complex 258 Clones (ST258, ST11, ST437) and Plasmids (IncFII, IncN, IncL/M) among Enterobacteriaceae Species in Brazil [J].
Andrade, Leonardo Neves ;
Curiao, Tania ;
Ferreira, Joseane Cristina ;
Longo, Juliana Mucedola ;
Climaco, Eduardo Carneiro ;
Martinez, Roberto ;
Bellissimo-Rodrigues, Fernando ;
Basile-Filho, Anibal ;
Evaristo, Marco Antonio ;
Del Peloso, Pedro F. ;
Ribeiro, Vanessa Bley ;
Barth, Afonso Luis ;
Paula, Milena Cristina ;
Baquero, Fernando ;
Canton, Rafael ;
da Costa Darini, Ana Lucia ;
Coque, Teresa M. .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2011, 55 (07) :3579-3583
[2]   Comparative and evolutionary analysis of plasmid pREN isolated from Lactobacillus rennini, a novel member of the theta-replicating pUCL287 family [J].
Asteri, Ioanna-Areti ;
Papadimitriou, Konstantinos ;
Boutou, Effrossyni ;
Pot, Bruno ;
Vorgias, Constantinos E. ;
Tsakalidou, Effie .
FEMS MICROBIOLOGY LETTERS, 2011, 318 (01) :18-26
[3]   The relationship between the volume of antimicrobial consumption in human communities and the frequency of resistance [J].
Austin, DJ ;
Kristinsson, KG ;
Anderson, RM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (03) :1152-1156
[4]   PSIB, AN ANTI-SOS PROTEIN, IS TRANSIENTLY EXPRESSED BY THE F-SEX FACTOR DURING ITS TRANSMISSION TO AN ESCHERICHIA-COLI K-12 RECIPIENT [J].
BAGDASARIAN, M ;
BAILONE, A ;
ANGULO, JF ;
SCHOLZ, P ;
BAGDASARIAN, M ;
DEVORET, R .
MOLECULAR MICROBIOLOGY, 1992, 6 (07) :885-893
[5]   SUPPRESSION OF INDUCTION OF SOS FUNCTIONS IN AN ESCHERICHIA-COLI TIF-1 MUTANT BY PLASMID-R100.1 [J].
BAGDASARIAN, M ;
DARI, R ;
FILIPOWICZ, W ;
GEORGE, J .
JOURNAL OF BACTERIOLOGY, 1980, 141 (02) :464-469
[6]   Conjugative DNA Transfer Induces the Bacterial SOS Response and Promotes Antibiotic Resistance Development through Integron Activation [J].
Baharoglu, Zeynep ;
Bikard, David ;
Mazel, Didier .
PLOS GENETICS, 2010, 6 (10) :1-10
[7]   PSIB POLYPEPTIDE PREVENTS ACTIVATION OF RECA PROTEIN IN ESCHERICHIA-COLI [J].
BAILONE, A ;
BACKMAN, A ;
SOMMER, S ;
CELERIER, J ;
BAGDASARIAN, MM ;
BAGDASARIAN, M ;
DEVORET, R .
MOLECULAR AND GENERAL GENETICS, 1988, 214 (03) :389-395
[8]   Ecology and Evolution as Targets: the Need for Novel Eco-Evo Drugs and Strategies To Fight Antibiotic Resistance [J].
Baquero, Fernando ;
Coque, Teresa M. ;
de la Cruz, Fernando .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2011, 55 (08) :3649-3660
[9]  
Barlow Miriam, 2009, V532, P397, DOI 10.1007/978-1-60327-853-9_23
[10]   Highways of gene sharing in prokaryotes [J].
Beiko, RG ;
Harlow, TJ ;
Ragan, MA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (40) :14332-14337