Diversity of Prophages in Dominant Staphylococcus aureus Clonal Lineages

被引:222
作者
Goerke, Christiane [1 ]
Pantucek, Roman [2 ]
Holtfreter, Silva [3 ]
Schulte, Berit [1 ]
Zink, Manuel [1 ]
Grumann, Dorothee [3 ]
Broeker, Barbara M. [3 ]
Doskar, Jiri [2 ]
Wolz, Christiane [1 ]
机构
[1] Univ Klinikum Tubingen, Inst Med Mikrobiol & Hyg, D-72076 Tubingen, Germany
[2] Masaryk Univ, Dept Genet & Mol Biol, Brno, Czech Republic
[3] Ernst Moritz Arndt Univ Greifswald, Inst Immunol & Transfus Med, Greifswald, Germany
关键词
RESTRICTION-MODIFICATION SYSTEM; PANTON-VALENTINE LEUKOCIDIN; METHICILLIN-RESISTANT; PHAGE CONVERSION; COMPLETE GENOMES; ENTEROTOXIN-A; TOXIN GENES; SEQUENCE; BACTERIOPHAGES; INFECTION;
D O I
10.1128/JB.01804-08
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Temperate bacteriophages play an important role in the pathogenicity of Staphylococcus aureus, for instance, by mediating the horizontal gene transfer of virulence factors. Here we established a classification scheme for staphylococcal prophages of the major Siphoviridae family based on integrase gene polymorphism. Seventy-one published genome sequences of staphylococcal phages were clustered into distinct integrase groups which were related to the chromosomal integration site and to the encoded virulence gene content. Analysis of three marker modules (lysogeny, tail, and lysis) for phage functional units revealed that these phages exhibit different degrees of genome mosaicism. The prevalence of prophages in a representative S. aureus strain collection consisting of 386 isolates of diverse origin was determined. By linking the phage content to dominant S. aureus clonal complexes we could show that the distribution of bacteriophages varied remarkably between lineages, indicating restriction-based barriers. A comparison of colonizing and invasive S. aureus strain populations revealed that hlb-converting phages were significantly more frequent in colonizing strains.
引用
收藏
页码:3462 / 3468
页数:7
相关论文
共 35 条
  • [1] Ackermann H. W., 1987, NATURAL GROUPS BACTE, V2
  • [2] Genome and virulence determinants of high virulence community-acquired MRSA
    Baba, T
    Takeuchi, F
    Kuroda, M
    Yuzawa, H
    Aoki, K
    Oguchi, A
    Nagai, Y
    Iwama, N
    Asano, K
    Naimi, T
    Kuroda, H
    Cui, L
    Yamamoto, K
    Hiramatsu, K
    [J]. LANCET, 2002, 359 (9320) : 1819 - 1827
  • [3] STAPHYLOCOCCAL ENTEROTOXIN-A IS ENCODED BY PHAGE
    BETLEY, MJ
    MEKALANOS, JJ
    [J]. SCIENCE, 1985, 229 (4709) : 185 - 187
  • [4] Comparative phage genomics and the evolution of Siphoviridae:: insights from dairy phages
    Brüssow, H
    Desiere, F
    [J]. MOLECULAR MICROBIOLOGY, 2001, 39 (02) : 213 - 222
  • [5] Prophage genomics
    Canchaya, C
    Proux, C
    Fournous, G
    Bruttin, A
    Brüssow, H
    [J]. MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS, 2003, 67 (02) : 238 - +
  • [6] COLEMAN DC, 1989, J GEN MICROBIOL, V135, P1679
  • [7] Sau421, a Bcgl-like restriction-modification system encoded by the Staphylococcus aureus quadruple-converting phage φ42
    Dempsey, RM
    Carroll, D
    Kong, HM
    Higgins, L
    Keane, CT
    Coleman, DC
    [J]. MICROBIOLOGY-SGM, 2005, 151 : 1301 - 1311
  • [8] Multilocus sequence typing for characterization of methicillin-resistant and methicillin-susceptible clones of Staphylococcus aureus
    Enright, MC
    Day, NPJ
    Davies, CE
    Peacock, SJ
    Spratt, BG
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 2000, 38 (03) : 1008 - 1015
  • [9] How clonal is Staphylococcus aureus?
    Feil, EJ
    Cooper, JE
    Grundmann, H
    Robinson, DA
    Enright, MC
    Berendt, T
    Peacock, SJ
    Smith, JM
    Murphy, M
    Spratt, BG
    Moore, CE
    Day, NPJ
    [J]. JOURNAL OF BACTERIOLOGY, 2003, 185 (11) : 3307 - 3316
  • [10] Increased frequency of genomic alterations in Staphylococcus aureus during chronic infection is in part due to phage mobilization
    Goerke, C
    Papenberg, SMY
    Dasbach, S
    Dietz, K
    Ziebach, R
    Kahl, BC
    Wolz, C
    [J]. JOURNAL OF INFECTIOUS DISEASES, 2004, 189 (04) : 724 - 734