Prevalence and characteristics of pks genotoxin gene cluster-positive clinical Klebsiella pneumoniae isolates in Taiwan
The pks gene cluster encodes enzymes responsible for the synthesis of colibactin, a genotoxin that has been shown to induce DNA damage and contribute to increased virulence. The present study investigated the prevalence of pks in clinical K. pneumoniae isolates from a national surveillance program in Taiwan, and identified microbiological and molecular factors associated with pks-carriage. The pks gene cluster was detected in 67 (16.7%) of 400 isolates from various specimen types. Multivariate analysis revealed that isolates of K1, K2, K20, and K62 capsular types (p < 0.001), and those more susceptible to antimicrobial agents (p = 0.001) were independent factors strongly associated with pks-carriage. Phylogenetic studies on the sequence type (ST) and pulsed-field gel electrophoresis patterns indicated that the pks-positive isolates belong to a clonal group of ST23 in K1, a locally expanding ST65 clone in K2, a ST268-related K20 group, and a highly clonal ST36:K62 group. Carriage of rmpA, iutC, and ybtA, the genes associated with hypervirulence, was significantly higher in the pks-positive isolates than the pks-negative isolates (95.5% vs. 13.2%, p < 0.001). Further studies to determine the presence of hypervirulent pks-bearing bacterial populations in the flora of community residents and their association with different disease entities may be warranted.
Medienart: |
E-Artikel |
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Erscheinungsjahr: |
2017 |
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Erschienen: |
2017 |
Enthalten in: |
Zur Gesamtaufnahme - volume:7 |
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Enthalten in: |
Scientific reports - 7(2017) vom: 24. Feb., Seite 43120 |
Sprache: |
Englisch |
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Beteiligte Personen: |
Chen, Ying-Tsong [VerfasserIn] |
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Links: |
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Themen: |
Bacterial Proteins |
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Anmerkungen: |
Date Completed 18.12.2018 Date Revised 18.12.2018 published: Electronic Citation Status MEDLINE |
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doi: |
10.1038/srep43120 |
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funding: |
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Förderinstitution / Projekttitel: |
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PPN (Katalog-ID): |
NLM269259465 |
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520 | |a The pks gene cluster encodes enzymes responsible for the synthesis of colibactin, a genotoxin that has been shown to induce DNA damage and contribute to increased virulence. The present study investigated the prevalence of pks in clinical K. pneumoniae isolates from a national surveillance program in Taiwan, and identified microbiological and molecular factors associated with pks-carriage. The pks gene cluster was detected in 67 (16.7%) of 400 isolates from various specimen types. Multivariate analysis revealed that isolates of K1, K2, K20, and K62 capsular types (p < 0.001), and those more susceptible to antimicrobial agents (p = 0.001) were independent factors strongly associated with pks-carriage. Phylogenetic studies on the sequence type (ST) and pulsed-field gel electrophoresis patterns indicated that the pks-positive isolates belong to a clonal group of ST23 in K1, a locally expanding ST65 clone in K2, a ST268-related K20 group, and a highly clonal ST36:K62 group. Carriage of rmpA, iutC, and ybtA, the genes associated with hypervirulence, was significantly higher in the pks-positive isolates than the pks-negative isolates (95.5% vs. 13.2%, p < 0.001). Further studies to determine the presence of hypervirulent pks-bearing bacterial populations in the flora of community residents and their association with different disease entities may be warranted | ||
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700 | 1 | |a Hsieh, Li-Yun |e verfasserin |4 aut | |
700 | 1 | |a Wang, Jann-Tay |e verfasserin |4 aut | |
700 | 1 | |a Shiau, Yih-Ru |e verfasserin |4 aut | |
700 | 1 | |a Wang, Hui-Ying |e verfasserin |4 aut | |
700 | 1 | |a Lin, Ann-Chi |e verfasserin |4 aut | |
700 | 1 | |a Lai, Jui-Fen |e verfasserin |4 aut | |
700 | 1 | |a Huang, I-Wen |e verfasserin |4 aut | |
700 | 1 | |a Lauderdale, Tsai-Ling |e verfasserin |4 aut | |
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