CTX prophages in classical biotype Vibrio cholerae:: Functional phage genes but dysfunctional phage genomes

被引:96
作者
Davis, BM
Moyer, KE
Boyd, EF
Waldor, MK
机构
[1] Tufts Univ, Sch Med, Howard Hughes Med Inst, Boston, MA 02111 USA
[2] New England Med Ctr, Div Geog Med & Infect Dis, Boston, MA 02111 USA
关键词
D O I
10.1128/JB.182.24.6992-6998.2000
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
CTX phi is a filamentous, lysogenic bacteriophage whose genome encodes cholera toxin, the primary virulence factor produced by Vibrio cholerae, CTX prophages in O1 El Tor and O139 strains of V. cholerae are found within arrays of genetically related elements integrated at a single locus within the V. cholerae large chromosome. The prophages of O1 El Tor and O139 strains generally yield infectious CTX phi. In contrast, O1 classical strains of V, cholerae do not produce CTX phi, although they produce cholera toxin and they contain CTX prophages integrated at two sites. We have identified the second site of CTX prophage integration in O1 classical strains and characterized the classical prophage arrays genetically and functionally. The genes of classical prophages encode functional forms of all of the proteins needed for production of CTX phi. Classical CTX prophages are present either as solitary prophages or as arrays of two truncated, fused prophages, RSI, a genetic element that is closely related to CTX phi and is often interspersed with CTX prophages in El Tor strains, was not detected in classical V,cholerae, Our model for CTX phi, production predicts that the CTX prophage arrangements in classical strains will not yield extrachromosomal CTX DNA and thus will not yield virions, and our experimental results confirm this prediction. Thus, failure of O1 classical strains of V, cholerae to produce CTX phi is due to overall deficiencies in the structures of the arrays of classical prophages, rather than to mutations affecting individual CTX prophage genes.
引用
收藏
页码:6992 / 6998
页数:7
相关论文
共 24 条
  • [1] AUSUBEL FM, 1990, CURRENT PROTOCOLS MO
  • [2] Barua Dhiman, 1992, P1
  • [3] Heterogeneity in the organization of the CTX genetic element in strains of Vibrio cholerae O139 Bengal isolated from Calcutta, India and Dhaka, Bangladesh and its possible link to the dissimilar incidence of O139 cholera in the two locales
    Basu, A
    Mukhopadhyay, AK
    Sharma, C
    Jyot, J
    Gupta, N
    Ghosh, A
    Bhattacharya, SK
    Takeda, Y
    Faruque, ASG
    Albert, MJ
    Nair, GB
    [J]. MICROBIAL PATHOGENESIS, 1998, 24 (03) : 175 - 183
  • [4] Basu A, 2000, FEMS MICROBIOL LETT, V182, P35, DOI 10.1111/j.1574-6968.2000.tb08869.x
  • [5] CLONING OF A GENE (ZOT) ENCODING A NEW TOXIN PRODUCED BY VIBRIO-CHOLERAE
    BAUDRY, B
    FASANO, A
    KETLEY, J
    KAPER, JB
    [J]. INFECTION AND IMMUNITY, 1992, 60 (02) : 428 - 434
  • [6] The Vibrio cholerae O139 Calcutta bacteriophage CTXφ is infectious and encodes a novel repressor
    Davis, BM
    Kimsey, HH
    Chang, W
    Waldor, MK
    [J]. JOURNAL OF BACTERIOLOGY, 1999, 181 (21) : 6779 - 6787
  • [7] CTXφ contains a hybrid genome derived from tandemly integrated elements
    Davis, BM
    Waldor, MK
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (15) : 8572 - 8577
  • [8] CHARACTERIZATION AND DISTRIBUTION OF THE HEMAGGLUTININS PRODUCED BY VIBRIO-CHOLERAE
    HANNE, LF
    FINKELSTEIN, RA
    [J]. INFECTION AND IMMUNITY, 1982, 36 (01) : 209 - 214
  • [9] DNA sequence of both chromosomes of the cholera pathogen Vibrio cholerae
    Heidelberg, JF
    Eisen, JA
    Nelson, WC
    Clayton, RA
    Gwinn, ML
    Dodson, RJ
    Haft, DH
    Hickey, EK
    Peterson, JD
    Umayam, L
    Gill, SR
    Nelson, KE
    Read, TD
    Tettelin, H
    Richardson, D
    Ermolaeva, MD
    Vamathevan, J
    Bass, S
    Qin, HY
    Dragoi, I
    Sellers, P
    McDonald, L
    Utterback, T
    Fleishmann, RD
    Nierman, WC
    White, O
    Salzberg, SL
    Smith, HO
    Colwell, RR
    Mekalanos, JJ
    Venter, JC
    Fraser, CM
    [J]. NATURE, 2000, 406 (6795) : 477 - 483
  • [10] CHOLERA
    KAPER, JB
    MORRIS, JG
    LEVINE, MM
    [J]. CLINICAL MICROBIOLOGY REVIEWS, 1995, 8 (01) : 48 - 86