Gerson, Stefanie, Lucassen, Kai, Wille, Julia, Nodari, Carolina S., Stefanik, Danuta, Nowak, Jennifer, Wille, Thorsten, Betts, Jonathan W., Roca, Ignasi ORCID: 0000-0002-1800-1576, Vila, Jordi, Cisneros, Jose M., Seifert, Harald and Higgins, Paul G. ORCID: 0000-0001-8677-9454 (2020). Diversity of amino acid substitutions in PmrCAB associated with colistin resistance in clinical isolates of Acinetobacter baumannii. Int. J. Antimicrob. Agents, 55 (3). AMSTERDAM: ELSEVIER. ISSN 1872-7913

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Abstract

This study aimed to investigate the mechanisms of colistin resistance in 64 Acinetobacter baumannii isolates obtained from patients with ventilator-associated pneumonia hospitalised in Greece, Italy and Spain. In total, 31 A. baumannii isolates were colistin-resistant. Several novel amino acid substitutions in PmrCAB were found in 27 colistin-resistant A. baumannii. Most substitutions were detected in PmrB, indicating the importance of the histidine kinase for colistin resistance. In two colistin-resistant isolates, 93 amino acid changes were observed in PmrCAB compared with A. baumannii ACICU, and homologous recombination across different clonal lineages was suggested. Analysis of gene expression revealed increased pmrC expression in isolates harbouring pmrCAB mutations. Complementation of A. baumannii ATCC 19606 and ATCC 17978 with a pmrAB variant revealed increased pmrC expression but unchanged colistin MICs, indicating additional unknown factors associated with colistin resistance. Moreover, a combination of PmrB and PmrC alterations was associated with very high colistin MICs, suggesting accumulation of mutations as the mechanism for high-level resistance. The pmrC homologue eptA was detected in 29 colistin-susceptible and 26 colistin-resistant isolates. ISAba1 was found upstream of eptA in eight colistin-susceptible and one colistin-resistant isolate and eptA was disrupted by ISAba125 in two colistin-resistant isolates. Whilst in most isolates an association of eptA with colistin resistance was excluded, in one isolate an amino acid substitution in EptA (R127L) combined with a point mutation in ISAba1 upstream of eptA contributed to elevated colistin MICs. This study helps to gain an insight into the diversity and complexity of colistin resistance in A. baumannii. (C) 2019 Elsevier B.V. and International Society of Chemotherapy. All rights reserved.

Item Type: Journal Article
Creators:
CreatorsEmailORCIDORCID Put Code
Gerson, StefanieUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Lucassen, KaiUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Wille, JuliaUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Nodari, Carolina S.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Stefanik, DanutaUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Nowak, JenniferUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Wille, ThorstenUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Betts, Jonathan W.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Roca, IgnasiUNSPECIFIEDorcid.org/0000-0002-1800-1576UNSPECIFIED
Vila, JordiUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Cisneros, Jose M.UNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Seifert, HaraldUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Higgins, Paul G.UNSPECIFIEDorcid.org/0000-0001-8677-9454UNSPECIFIED
URN: urn:nbn:de:hbz:38-343042
DOI: 10.1016/j.ijantimicag.2019.105862
Journal or Publication Title: Int. J. Antimicrob. Agents
Volume: 55
Number: 3
Date: 2020
Publisher: ELSEVIER
Place of Publication: AMSTERDAM
ISSN: 1872-7913
Language: English
Faculty: Unspecified
Divisions: Unspecified
Subjects: no entry
Uncontrolled Keywords:
KeywordsLanguage
VENTILATOR-ASSOCIATED PNEUMONIA; POLYMYXIN RESISTANCE; EFFLUX; IDENTIFICATION; MUTATIONS; EMERGENCE; STRAINS; OPERON; PART; ADERMultiple languages
Infectious Diseases; Microbiology; Pharmacology & PharmacyMultiple languages
URI: http://kups.ub.uni-koeln.de/id/eprint/34304

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