Umeå universitets logga

umu.sePublikationer
Driftmeddelande
För närvarande är det driftstörningar. Felsökning pågår.
Ändra sökning
RefereraExporteraLänk till posten
Permanent länk

Direktlänk
Referera
Referensformat
  • apa
  • ieee
  • vancouver
  • Annat format
Fler format
Språk
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Annat språk
Fler språk
Utmatningsformat
  • html
  • text
  • asciidoc
  • rtf
Molecular epidemiology and antimicrobial resistance features of Acinetobacter baumannii clinical isolates from Pakistan
Umeå universitet, Medicinska fakulteten, Molekylär Infektionsmedicin, Sverige (MIMS). Umeå universitet, Medicinska fakulteten, Umeå Centre for Microbial Research (UCMR).ORCID-id: 0000-0001-8867-658X
Department of Microbiology, University of Health Sciences, Lahore, Pakistan.
Umeå universitet, Medicinska fakulteten, Umeå Centre for Microbial Research (UCMR). Umeå universitet, Medicinska fakulteten, Molekylär Infektionsmedicin, Sverige (MIMS).
Umeå universitet, Medicinska fakulteten, Umeå Centre for Microbial Research (UCMR). Umeå universitet, Medicinska fakulteten, Molekylär Infektionsmedicin, Sverige (MIMS).ORCID-id: 0000-0002-2991-8072
Visa övriga samt affilieringar
2020 (Engelska)Ingår i: Annals of Clinical Microbiology and Antimicrobials, E-ISSN 1476-0711, Vol. 19, artikel-id 2Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

Background: Acinetobacter baumannii is a Gram-negative opportunistic pathogen with a notorious reputation of being resistant to antimicrobial agents. The capability of A. baumannii to persist and disseminate between healthcare settings has raised a major concern worldwide.

Methods: Our study investigated the antibiotic resistance features and molecular epidemiology of 52 clinical isolates of A. baumannii collected in Pakistan between 2013 and 2015. Antimicrobial susceptibility patterns were determined by the agar disc diffusion method. Comparative sequence analyses of the ampC and blaOXA-51-like alleles were used to assign the isolates into clusters. The whole genomes of 25 representative isolates were sequenced using the MiSeq Desktop Sequencer. Free online applications were used to determine the phylogeny of genomic sequences, retrieve the multilocus sequence types (ST), and detect acquired antimicrobial resistance genes.

Results: Overall, the isolates were grouped into 7 clusters and 3 sporadic isolates. The largest cluster, Ab-Pak-cluster-1 (blaOXA-66 and ISAba1-ampC-19) included 24 isolates, belonged to ST2 and International clone (IC) II, and was distributed between two geographical far-off cities, Lahore and Peshawar. Ab-Pak-clusters-2 (blaOXA-66, ISAba1-ampC-2), and -3 (blaOXA-66, ISAba1-ampC-20) and the individual isolate Ab-Pak-Lah-01 (ISAba1-blaOXA-66, ISAba1-ampC-2) were also assigned to ST2 and IC II. On the other hand, Ab-Pak-clusters-4 (blaOXA-69, ampC-1), -5 (blaOXA-69, ISAba1-ampC-78), and -6A (blaOXA-371, ISAba1-ampC-3) belonged to ST1, while Ab-Pak-cluster-6B (blaOXA-371, ISAba1-ampC-8) belonged to ST1106, with both ST1 and ST1106 being members of IC I. Five isolates belonged to Ab-Pak-cluster-7 (blaOXA-65, ampC-43). This cluster corresponded to ST158, showed a well-delineated position on the genomic phylogenetic tree, and was equipped with several antimicrobial resistance genes including blaOXA-23 and blaGES-11.

Conclusions: Our study detected the occurrence of 7 clusters of A. baumannii in Pakistan. Altogether, 6/7 of the clusters and 45/52 (86.5%) of the isolates belonged to IC I (n = 9) or II (n = 36), making Pakistan no exception to the global domination of these two clones. The onset of ST158 in Pakistan marked a geographical dispersal of this clone beyond the Middle East and brought up the need for a detailed characterization.

Ort, förlag, år, upplaga, sidor
Springer, 2020. Vol. 19, artikel-id 2
Nyckelord [en]
Carbapenem-resistance, Strain typing, International clone, Phylogeny
Nationell ämneskategori
Mikrobiologi inom det medicinska området
Identifikatorer
URN: urn:nbn:se:umu:diva-168832DOI: 10.1186/s12941-019-0344-7ISI: 000513637900001PubMedID: 31941492Scopus ID: 2-s2.0-85077941900OAI: oai:DiVA.org:umu-168832DiVA, id: diva2:1415686
Forskningsfinansiär
Vetenskapsrådet, 2015-03007Vetenskapsrådet, 2015-06824Vetenskapsrådet, 2018-02914Vetenskapsrådet, 2007-8673Vetenskapsrådet, 2016-06598Kempestiftelserna, JCK-1527Kempestiftelserna, JCK-1724Tillgänglig från: 2020-03-19 Skapad: 2020-03-19 Senast uppdaterad: 2024-02-15Bibliografiskt granskad

Open Access i DiVA

fulltext(1173 kB)361 nedladdningar
Filinformation
Filnamn FULLTEXT01.pdfFilstorlek 1173 kBChecksumma SHA-512
b73522a74dd3ff8d439bca5cfdd5a1627fe8e2be912578acbc5bb14e51c0621bd2825dce0a693cd93a62ab4763c07b159fc0c5710cfe54fbd943574b762d2e92
Typ fulltextMimetyp application/pdf

Övriga länkar

Förlagets fulltextPubMedScopus

Person

Karah, NabilWai, Sun NyuntUhlin, Bernt EricAhmad, Irfan

Sök vidare i DiVA

Av författaren/redaktören
Karah, NabilWai, Sun NyuntUhlin, Bernt EricAhmad, Irfan
Av organisationen
Molekylär Infektionsmedicin, Sverige (MIMS)Umeå Centre for Microbial Research (UCMR)
I samma tidskrift
Annals of Clinical Microbiology and Antimicrobials
Mikrobiologi inom det medicinska området

Sök vidare utanför DiVA

GoogleGoogle Scholar
Totalt: 361 nedladdningar
Antalet nedladdningar är summan av nedladdningar för alla fulltexter. Det kan inkludera t.ex tidigare versioner som nu inte längre är tillgängliga.

doi
pubmed
urn-nbn

Altmetricpoäng

doi
pubmed
urn-nbn
Totalt: 652 träffar
RefereraExporteraLänk till posten
Permanent länk

Direktlänk
Referera
Referensformat
  • apa
  • ieee
  • vancouver
  • Annat format
Fler format
Språk
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Annat språk
Fler språk
Utmatningsformat
  • html
  • text
  • asciidoc
  • rtf