Clostridium botulinum group III: a group with dual identity shaped by plasmids, phages and mobile elements

被引:87
作者
Skarin, Hanna [1 ,2 ]
Hafstrom, Therese [1 ]
Westerberg, Josefina [1 ]
Segerman, Bo [1 ]
机构
[1] Natl Vet Inst SVA, Dept Bacteriol, Uppsala, Sweden
[2] Swedish Univ Agr Sci SLU, Dept Biomed Sci & Vet Publ Hlth, Uppsala, Sweden
来源
BMC GENOMICS | 2011年 / 12卷
关键词
NEUROTOXIN COMPLEX GENES; GENOME SEQUENCE; INSERTION; PATHOGEN; TOXIN; PERFRINGENS; STRAINS; ARTEMIS; NOVYI; TOOL;
D O I
10.1186/1471-2164-12-185
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: Clostridium botulinum strains can be divided into four physiological groups that are sufficiently diverged to be considered as separate species. Here we present the first complete genome of a C. botulinum strain from physiological group III, causing animal botulism. We also compare the sequence to three new draft genomes from the same physiological group. Results: The 2.77 Mb chromosome was highly conserved between the isolates and also closely related to that of C. novyi. However, the sequence was very different from the human C. botulinum group genomes. Replication-directed translocations were rare and conservation of synteny was high. The largest difference between C. botulinum group III isolates occurred within their surprisingly large plasmidomes and in the pattern of mobile elements insertions. Five plasmids, constituting 13.5% of the total genetic material, were present in the completed genome. Interestingly, the set of plasmids differed compared to other isolates. The largest plasmid, the botulinum-neurotoxin carrying prophage, was conserved at a level similar to that of the chromosome while the medium-sized plasmids seemed to be undergoing faster genetic drift. These plasmids also contained more mobile elements than other replicons. Several toxins and resistance genes were identified, many of which were located on the plasmids. Conclusions: The completion of the genome of C. botulinum group III has revealed it to be a genome with dual identity. It belongs to the pathogenic species C. botulinum, but as a genotypic species it should also include C. novyi and C. haemolyticum. The genotypic species share a conserved chromosomal core that can be transformed into various pathogenic variants by modulation of the highly plastic plasmidome.
引用
收藏
页数:13
相关论文
共 43 条
[1]   Genetic variation and cross-reactivity of Clostridium septicum alpha-toxin [J].
Amimoto, K ;
Sasaki, Y ;
Fukuyama, S ;
Tamura, Y .
VETERINARY MICROBIOLOGY, 2006, 114 (1-2) :51-59
[2]   Botulinum toxin as a biological weapon - Medical and public health management [J].
Arnon, SS ;
Schechter, R ;
Inglesby, TV ;
Henderson, DA ;
Bartlett, JG ;
Ascher, MS ;
Eitzen, E ;
Fine, AD ;
Hauer, J ;
Layton, M ;
Lillibridge, S ;
Osterholm, MT ;
O'Toole, T ;
Parker, G ;
Perl, TM ;
Russell, PK ;
Swerdlow, DL ;
Tonat, K .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2001, 285 (08) :1059-1070
[3]   A GENERAL-METHOD FOR DETECTING AND SIZING LARGE PLASMIDS [J].
BARTON, BM ;
HARDING, GP ;
ZUCCARELLI, AJ .
ANALYTICAL BIOCHEMISTRY, 1995, 226 (02) :235-240
[4]   The genome and transcriptomes of the anti-tumor agent Clostridium novyi-NT [J].
Bettegowda, Chetan ;
Huang, Xin ;
Lin, Jimmy ;
Cheong, Ian ;
Kohli, Manu ;
Szabo, Stephen A. ;
Zhang, Xiaosong ;
Diaz, Luis A., Jr. ;
Velculescu, Victor E. ;
Parmigiani, Giovanni ;
Kinzler, Kenneth W. ;
Vogelstein, Bert ;
Zhou, Shibin .
NATURE BIOTECHNOLOGY, 2006, 24 (12) :1573-1580
[5]   Independent evolution of neurotoxin and flagellar genetic loci in proteolytic Clostridium botulinum [J].
Carter, Andrew T. ;
Paul, Catherine J. ;
Mason, David R. ;
Twine, Susan M. ;
Alston, Mark J. ;
Logan, Susan M. ;
Austin, John W. ;
Peck, Michael W. .
BMC GENOMICS, 2009, 10
[6]   DNAPlotter: circular and linear interactive genome visualization [J].
Carver, Tim ;
Thomson, Nick ;
Bleasby, Alan ;
Berriman, Matthew ;
Parkhill, Julian .
BIOINFORMATICS, 2009, 25 (01) :119-120
[7]   ACT: the Artemis comparison tool [J].
Carver, TJ ;
Rutherford, KM ;
Berriman, M ;
Rajandream, MA ;
Barrell, BG ;
Parkhill, J .
BIOINFORMATICS, 2005, 21 (16) :3422-3423
[8]  
Collins MD, 1998, J APPL MICROBIOL, V84, P5, DOI 10.1046/j.1365-2672.1997.00313.x
[9]   Improved microbial gene identification with GLIMMER [J].
Delcher, AL ;
Harmon, D ;
Kasif, S ;
White, O ;
Salzberg, SL .
NUCLEIC ACIDS RESEARCH, 1999, 27 (23) :4636-4641
[10]  
DINTER VZ, 1951, NORD VET MED, V3, P297