Sequence of Two Plasmids from Clostridium perfringens Chicken Necrotic Enteritis Isolates and Comparison with C. perfringens Conjugative Plasmids
Parreira VR, Costa M, Eikmeyer FG, Blom J, Prescott JF (2012)
PLoS ONE 7(11): e49753.
Zeitschriftenaufsatz
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Autor*in
Parreira, Valeria R.;
Costa, Marcio;
Eikmeyer, Felix GregorUniBi ;
Blom, JochenUniBi;
Prescott, John F.
Einrichtung
Abstract / Bemerkung
Twenty-six isolates of Clostridium perfringens of different MLST types from chickens with necrotic enteritis (NE) (15 netB-positive) or from healthy chickens (6 netB-positive, 5 netB-negative) were found to contain 1–4 large plasmids, with most netB-positive isolates containing 3 large and variably sized plasmids which were more numerous and larger than plasmids in netB-negative isolates. NetB and cpb2 were found on different plasmids consistent with previous studies. The pathogenicity locus NELoc1, which includes netB, was largely conserved in these plasmids whereas NeLoc3, present in the cpb2 containing plasmids, was less well conserved. A netB-positive and a cpb2-positive plasmid were likely to be conjugative, and the plasmids were completely sequenced. Both plasmids possessed the intact tcp conjugative region characteristic of C. perfringens conjugative plasmids. Comparative genomic analysis of nine CpCPs, including the two plasmids described here, showed extensive gene rearrangements including pathogenicity locus and accessory gene insertions around rather than within the backbone region. The pattern that emerges from this analysis is that the major toxin-containing regions of the variety of virulence-associated CpCPs are organized as complex pathogenicity loci. How these different but related CpCPs can co-exist in the same host has been an unanswered question. Analysis of the replication-partition region of these plasmids suggests that this region controls plasmid incompatibility, and that CpCPs can be grouped into at least four incompatibility groups.
Erscheinungsjahr
2012
Zeitschriftentitel
PLoS ONE
Band
7
Ausgabe
11
Art.-Nr.
e49753
ISSN
1932-6203
eISSN
1932-6203
Page URI
https://pub.uni-bielefeld.de/record/2542210
Zitieren
Parreira VR, Costa M, Eikmeyer FG, Blom J, Prescott JF. Sequence of Two Plasmids from Clostridium perfringens Chicken Necrotic Enteritis Isolates and Comparison with C. perfringens Conjugative Plasmids. PLoS ONE. 2012;7(11): e49753.
Parreira, V. R., Costa, M., Eikmeyer, F. G., Blom, J., & Prescott, J. F. (2012). Sequence of Two Plasmids from Clostridium perfringens Chicken Necrotic Enteritis Isolates and Comparison with C. perfringens Conjugative Plasmids. PLoS ONE, 7(11), e49753. doi:10.1371/journal.pone.0049753
Parreira, Valeria R., Costa, Marcio, Eikmeyer, Felix Gregor, Blom, Jochen, and Prescott, John F. 2012. “Sequence of Two Plasmids from Clostridium perfringens Chicken Necrotic Enteritis Isolates and Comparison with C. perfringens Conjugative Plasmids”. PLoS ONE 7 (11): e49753.
Parreira, V. R., Costa, M., Eikmeyer, F. G., Blom, J., and Prescott, J. F. (2012). Sequence of Two Plasmids from Clostridium perfringens Chicken Necrotic Enteritis Isolates and Comparison with C. perfringens Conjugative Plasmids. PLoS ONE 7:e49753.
Parreira, V.R., et al., 2012. Sequence of Two Plasmids from Clostridium perfringens Chicken Necrotic Enteritis Isolates and Comparison with C. perfringens Conjugative Plasmids. PLoS ONE, 7(11): e49753.
V.R. Parreira, et al., “Sequence of Two Plasmids from Clostridium perfringens Chicken Necrotic Enteritis Isolates and Comparison with C. perfringens Conjugative Plasmids”, PLoS ONE, vol. 7, 2012, : e49753.
Parreira, V.R., Costa, M., Eikmeyer, F.G., Blom, J., Prescott, J.F.: Sequence of Two Plasmids from Clostridium perfringens Chicken Necrotic Enteritis Isolates and Comparison with C. perfringens Conjugative Plasmids. PLoS ONE. 7, : e49753 (2012).
Parreira, Valeria R., Costa, Marcio, Eikmeyer, Felix Gregor, Blom, Jochen, and Prescott, John F. “Sequence of Two Plasmids from Clostridium perfringens Chicken Necrotic Enteritis Isolates and Comparison with C. perfringens Conjugative Plasmids”. PLoS ONE 7.11 (2012): e49753.
Daten bereitgestellt von European Bioinformatics Institute (EBI)
UNIPROT
151 Einträge gefunden, die diesen Artikel zitieren von denen 10 angezeigt werden
Uncharacterized protein (UNIPROT: G5DS68)
Organism: Clostridium perfringens
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Organism: Clostridium perfringens
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Conjugation protein TcpC (UNIPROT: K9MF44)
Organism: Clostridium perfringens
Download in FASTA format
Organism: Clostridium perfringens
Download in FASTA format
Uncharacterized protein (UNIPROT: K9MF52)
Organism: Clostridium perfringens
Download in FASTA format
Organism: Clostridium perfringens
Download in FASTA format
Uncharacterized protein (UNIPROT: F8UNJ1)
Organism: Clostridium perfringens
Download in FASTA format
Organism: Clostridium perfringens
Download in FASTA format
Tn3 transposase DDE domain protein (UNIPROT: F8UNI1)
Organism: Clostridium perfringens
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Organism: Clostridium perfringens
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Uncharacterized protein (UNIPROT: Q4ZFS0)
Organism: Clostridium perfringens
Download in FASTA format
Organism: Clostridium perfringens
Download in FASTA format
Uncharacterized protein (UNIPROT: G5DSA9)
Organism: Clostridium perfringens
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Organism: Clostridium perfringens
Download in FASTA format
Uncharacterized protein (UNIPROT: K9MEF3)
Organism: Clostridium perfringens
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Organism: Clostridium perfringens
Download in FASTA format
EMBL
2 Einträge gefunden, die diesen Artikel zitieren
9 Zitationen in Europe PMC
Daten bereitgestellt von Europe PubMed Central.
Plasmid Characterization and Chromosome Analysis of Two netF+ Clostridium perfringens Isolates Associated with Foal and Canine Necrotizing Enteritis.
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A novel pore-forming toxin in type A Clostridium perfringens is associated with both fatal canine hemorrhagic gastroenteritis and fatal foal necrotizing enterocolitis.
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Two novel membrane proteins, TcpD and TcpE, are essential for conjugative transfer of pCW3 in Clostridium perfringens.
Wisniewski JA, Teng WL, Bannam TL, Rood JI., J. Bacteriol. 197(4), 2015
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Hassan KA, Elbourne LD, Tetu SG, Melville SB, Rood JI, Paulsen IT., Res. Microbiol. 166(4), 2015
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