Molecular epidemiology of carbapenem non-susceptible Acinetobacter nosocomialis in a medical center in Taiwan
The mechanism by which carbapenem non-susceptible Acinetobacter nosocomialis (CNSAN) is disseminated is rarely described in the literature. In this study, we delineated the molecular epidemiology of CNSAN isolated from patients in a medical center in Taiwan. Fifty-four non-duplicate bloodstream isolates of CNSAN were collected at the Taipei Veterans General Hospital between 2001 and 2007. Pulsed-field gel electrophoresis (PFGE) was performed to determine their clonal relationship. Carbapenem-resistance genes and associated genetic structures were detected by polymerase chain reaction (PCR) mapping. Southern hybridization was performed to determine the plasmid location of carbapenem-resistance genes. Transmissibility of these genes to Acinetobacterbaumannii was demonstrated by conjugation tests. The overall carbapenem non-susceptibility rate among A. nosocomialis isolates during the study period was 21.6% (54/250). PFGE revealed three major pulsotypes: H (n=23), I (n=10), and K (n=8). The most common carbapenem-resistance gene was blaOXA-58 (43/54, 79.6%), containing an upstream insertion sequence IS1006 and a truncated ISAba3 (IS1006-ΔISAba3-like-blaOXA-58). All isolates belonging to the pulsotypes H, I, and K carried plasmid located IS1006-ΔISAba3-like-blaOXA-58. A common plasmid carrying ISAba1-blaOXA-82 was found in six isolates, which belonged to five pulsotypes. A type 1 integron that carried blaIMP-1 was detected in different plasmids of seven isolates, which belonged to five pulsotypes. Plasmids carrying these carbapenem-resistant determinants were transmissible from A. nosocomialis to A. baumannii via conjugation. In this medical center, CNSAN mainly emerged through clonal dissemination; propagation of plasmids and integrons carrying carbapenem-resistant determinants played a minor role. This study showed that plasmids carrying carbapenem-resistant determinants are transmissible from A. nosocomialis to A. baumannii..
Medienart: |
Artikel |
---|
Erscheinungsjahr: |
2015 |
---|---|
Erschienen: |
2015 |
Enthalten in: |
Zur Gesamtaufnahme - volume:31 |
---|---|
Enthalten in: |
Infection, genetics and evolution - 31(2015), Seite 305-311 |
Sprache: |
Englisch |
---|
Beteiligte Personen: |
Yang, Ya-Sung [VerfasserIn] |
---|
Links: |
---|
doi: |
10.1016/j.meegid.2015.02.017 |
---|
funding: |
|
---|---|
Förderinstitution / Projekttitel: |
|
PPN (Katalog-ID): |
OLC1961333473 |
---|
LEADER | 01000caa a2200265 4500 | ||
---|---|---|---|
001 | OLC1961333473 | ||
003 | DE-627 | ||
005 | 20230519011006.0 | ||
007 | tu | ||
008 | 160206s2015 xx ||||| 00| ||eng c | ||
024 | 7 | |a 10.1016/j.meegid.2015.02.017 |2 doi | |
028 | 5 | 2 | |a PQ20160617 |
035 | |a (DE-627)OLC1961333473 | ||
035 | |a (DE-599)GBVOLC1961333473 | ||
035 | |a (PRQ)c1282-e16754711993e24ac12dd5b1818366b9ec941e7d718afb1ff189d8394900b3c40 | ||
035 | |a (KEY)0512118320150000031000000305molecularepidemiologyofcarbapenemnonsusceptibleaci | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
082 | 0 | 4 | |a 570 |q ZDB |
100 | 1 | |a Yang, Ya-Sung |e verfasserin |4 aut | |
245 | 1 | 0 | |a Molecular epidemiology of carbapenem non-susceptible Acinetobacter nosocomialis in a medical center in Taiwan |
264 | 1 | |c 2015 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a ohne Hilfsmittel zu benutzen |b n |2 rdamedia | ||
338 | |a Band |b nc |2 rdacarrier | ||
520 | |a The mechanism by which carbapenem non-susceptible Acinetobacter nosocomialis (CNSAN) is disseminated is rarely described in the literature. In this study, we delineated the molecular epidemiology of CNSAN isolated from patients in a medical center in Taiwan. Fifty-four non-duplicate bloodstream isolates of CNSAN were collected at the Taipei Veterans General Hospital between 2001 and 2007. Pulsed-field gel electrophoresis (PFGE) was performed to determine their clonal relationship. Carbapenem-resistance genes and associated genetic structures were detected by polymerase chain reaction (PCR) mapping. Southern hybridization was performed to determine the plasmid location of carbapenem-resistance genes. Transmissibility of these genes to Acinetobacterbaumannii was demonstrated by conjugation tests. The overall carbapenem non-susceptibility rate among A. nosocomialis isolates during the study period was 21.6% (54/250). PFGE revealed three major pulsotypes: H (n=23), I (n=10), and K (n=8). The most common carbapenem-resistance gene was blaOXA-58 (43/54, 79.6%), containing an upstream insertion sequence IS1006 and a truncated ISAba3 (IS1006-ΔISAba3-like-blaOXA-58). All isolates belonging to the pulsotypes H, I, and K carried plasmid located IS1006-ΔISAba3-like-blaOXA-58. A common plasmid carrying ISAba1-blaOXA-82 was found in six isolates, which belonged to five pulsotypes. A type 1 integron that carried blaIMP-1 was detected in different plasmids of seven isolates, which belonged to five pulsotypes. Plasmids carrying these carbapenem-resistant determinants were transmissible from A. nosocomialis to A. baumannii via conjugation. In this medical center, CNSAN mainly emerged through clonal dissemination; propagation of plasmids and integrons carrying carbapenem-resistant determinants played a minor role. This study showed that plasmids carrying carbapenem-resistant determinants are transmissible from A. nosocomialis to A. baumannii. | ||
540 | |a Nutzungsrecht: Copyright © 2015 Elsevier B.V. All rights reserved. | ||
650 | 4 | |a Acinetobacter - isolation & purification | |
650 | 4 | |a Acinetobacter Infections - epidemiology | |
650 | 4 | |a Acinetobacter Infections - microbiology | |
650 | 4 | |a Acinetobacter - drug effects | |
650 | 4 | |a Acinetobacter - genetics | |
650 | 4 | |a Acinetobacter - classification | |
650 | 4 | |a Carbapenems - pharmacology | |
700 | 1 | |a Lee, Yi-Tzu |4 oth | |
700 | 1 | |a Wang, Yung-Chih |4 oth | |
700 | 1 | |a Chiu, Chun-Hsiang |4 oth | |
700 | 1 | |a Kuo, Shu-Chen |4 oth | |
700 | 1 | |a Sun, Jun-Ren |4 oth | |
700 | 1 | |a Yin, Ti |4 oth | |
700 | 1 | |a Chen, Te-Li |4 oth | |
700 | 1 | |a Lin, Jung-Chung |4 oth | |
700 | 1 | |a Fung, Chang-Phone |4 oth | |
700 | 1 | |a Chang, Feng-Yee |4 oth | |
773 | 0 | 8 | |i Enthalten in |t Infection, genetics and evolution |d Amsterdam u.a.] : Elsevier, 2001 |g 31(2015), Seite 305-311 |w (DE-627)325568022 |w (DE-600)2037068-4 |x 1567-1348 |7 nnns |
773 | 1 | 8 | |g volume:31 |g year:2015 |g pages:305-311 |
856 | 4 | 1 | |u http://dx.doi.org/10.1016/j.meegid.2015.02.017 |3 Volltext |
856 | 4 | 2 | |u http://www.ncbi.nlm.nih.gov/pubmed/25724091 |
912 | |a GBV_USEFLAG_A | ||
912 | |a SYSFLAG_A | ||
912 | |a GBV_OLC | ||
912 | |a SSG-OLC-PHA | ||
912 | |a SSG-OLC-DE-84 | ||
912 | |a GBV_ILN_4219 | ||
951 | |a AR | ||
952 | |d 31 |j 2015 |h 305-311 |