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Whole genome sequence analysis of two Acinetobacter oleivorans clinical isolates from Terengganu, Malaysia, revealed the carriage of several virulence factors

Whole genome sequence analysis of two Acinetobacter oleivorans clinical isolates from Terengganu, Malaysia, revealed the carriage of several virulence factors
Whole genome sequence analysis of two Acinetobacter oleivorans clinical isolates from Terengganu, Malaysia, revealed the carriage of several virulence factors
Intro
Acinetobacter oleivorans is an environmental isolate that has rarely been reported to cause human infections, unlike the more notorious nosocomial pathogen, Acinetobacter baumannii. In this study, two clinical isolates of A. oleivorans from Hospital Sultanah Nur Zahirah in Terengganu were subjected to whole genome sequencing and the resulting sequences analysed.

Methods
A. oleivorans AC1583 and AC1885 were both isolated from the sputum of infected patients with pneumonia in 2015 and 2018, respectively. The isolates were initially identified as A. oleivorans by rpoB gene sequencing. Antimicrobial susceptibility was tested using a panel of 21 antibiotics encompassing 8
antimicrobial classes. Genome sequencing was performed on the Illumina HiSeq platform and assembled using Unicycler v.0.4.8.

Findings
AC1583 was susceptible to all tested antibiotics whereas AC1885 only displayed resistance to trimethoprim/sulfamethoxazole. The assembled genome size for AC1583 was 4,200,796 bp and 4,287,299 bp for AC1885. Multilocus sequence typing (MLST) using the Pasteur scheme indicated that AC1583 and AC1885 were typed as ST1616 and ST1617, respectively. Phylogenetic analysis showed that AC1583 and AC1885 were closely related to clinical isolates from Japan (A. oleivorans TUM15450) and the United States (A. oleivorans ACIN00177), respectively. Several virulence-associated genes were identified from the genome sequences of AC1583 and AC1885, and these include exotoxin genes such as phospholipase C and catalase, various genes for biofilm formation, immune modulation, and heme utilisation. AC1583 also harboured a small 8,731 bp plasmid, pAC1583-1, that was identical with a putative virulence-associated plasmid initially found in A. baumannii which harboured genes encoding a tonB-dependent receptor and sel1 repeat protein. This plasmid was absent in AC1885, which harboured a 11,715 bp cryptic plasmid designated pAC1885-1 instead.

Discussion
Conclusion
Despite its susceptibility to most antimicrobials, A. oleivorans was still capable of causing infections due likely to its carriage of several virulence factors and thus warrants vigilance.

Funding: FRGS/1/2018/SKK11/UNISZA/01/1
Mohd Rani, Farahiyah
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Rahman, N.I.A.
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Ismail, S.
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Othman, N.
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Cleary, David
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Abdullah, F.H.
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Clarke, Stuart C.
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Yeo, C.C.
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Mohd Rani, Farahiyah
5e43dfa9-8f75-4748-94b6-cb5725c14619
Rahman, N.I.A.
c37f86f5-4026-4951-b72d-e3dfb6b2dd7c
Ismail, S.
f49625b6-2a20-4958-b346-c7c65f7fda75
Othman, N.
b5e016a9-b53a-4f0c-837d-ca3bba030316
Cleary, David
f4079c6d-d54b-4108-b346-b0069035bec0
Abdullah, F.H.
c4595568-d50b-4cf6-9b58-236ba99ba82f
Clarke, Stuart C.
f7d7f7a2-4b1f-4b36-883a-0f967e73fb17
Yeo, C.C.
6d5f4874-8d37-4953-a549-39d768db22d3

Mohd Rani, Farahiyah, Rahman, N.I.A., Ismail, S., Othman, N., Cleary, David, Abdullah, F.H., Clarke, Stuart C. and Yeo, C.C. (2022) Whole genome sequence analysis of two Acinetobacter oleivorans clinical isolates from Terengganu, Malaysia, revealed the carriage of several virulence factors. ISID Congress 2022, Kuala Lumpur, Kuala Lumpur, Malaysia. 17 - 20 Nov 2022. (In Press)

Record type: Conference or Workshop Item (Poster)

Abstract

Intro
Acinetobacter oleivorans is an environmental isolate that has rarely been reported to cause human infections, unlike the more notorious nosocomial pathogen, Acinetobacter baumannii. In this study, two clinical isolates of A. oleivorans from Hospital Sultanah Nur Zahirah in Terengganu were subjected to whole genome sequencing and the resulting sequences analysed.

Methods
A. oleivorans AC1583 and AC1885 were both isolated from the sputum of infected patients with pneumonia in 2015 and 2018, respectively. The isolates were initially identified as A. oleivorans by rpoB gene sequencing. Antimicrobial susceptibility was tested using a panel of 21 antibiotics encompassing 8
antimicrobial classes. Genome sequencing was performed on the Illumina HiSeq platform and assembled using Unicycler v.0.4.8.

Findings
AC1583 was susceptible to all tested antibiotics whereas AC1885 only displayed resistance to trimethoprim/sulfamethoxazole. The assembled genome size for AC1583 was 4,200,796 bp and 4,287,299 bp for AC1885. Multilocus sequence typing (MLST) using the Pasteur scheme indicated that AC1583 and AC1885 were typed as ST1616 and ST1617, respectively. Phylogenetic analysis showed that AC1583 and AC1885 were closely related to clinical isolates from Japan (A. oleivorans TUM15450) and the United States (A. oleivorans ACIN00177), respectively. Several virulence-associated genes were identified from the genome sequences of AC1583 and AC1885, and these include exotoxin genes such as phospholipase C and catalase, various genes for biofilm formation, immune modulation, and heme utilisation. AC1583 also harboured a small 8,731 bp plasmid, pAC1583-1, that was identical with a putative virulence-associated plasmid initially found in A. baumannii which harboured genes encoding a tonB-dependent receptor and sel1 repeat protein. This plasmid was absent in AC1885, which harboured a 11,715 bp cryptic plasmid designated pAC1885-1 instead.

Discussion
Conclusion
Despite its susceptibility to most antimicrobials, A. oleivorans was still capable of causing infections due likely to its carriage of several virulence factors and thus warrants vigilance.

Funding: FRGS/1/2018/SKK11/UNISZA/01/1

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#871 WHOLE GENOME SEQUENCE ANALYSIS OF TWO ACINETOBACTER OLEIVORANS CLINICAL ISOLATES FROM TERENGGANU - Accepted Manuscript
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More information

Submitted date: 3 October 2022
Accepted/In Press date: 3 October 2022
Venue - Dates: ISID Congress 2022, Kuala Lumpur, Kuala Lumpur, Malaysia, 2022-11-17 - 2022-11-20

Identifiers

Local EPrints ID: 471315
URI: http://eprints.soton.ac.uk/id/eprint/471315
PURE UUID: ec4d78d1-7677-42a2-82ea-f80732ea1a16
ORCID for David Cleary: ORCID iD orcid.org/0000-0003-4533-0700
ORCID for Stuart C. Clarke: ORCID iD orcid.org/0000-0002-7009-1548

Catalogue record

Date deposited: 02 Nov 2022 17:48
Last modified: 17 Mar 2024 03:35

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Contributors

Author: Farahiyah Mohd Rani
Author: N.I.A. Rahman
Author: S. Ismail
Author: N. Othman
Author: David Cleary ORCID iD
Author: F.H. Abdullah
Author: C.C. Yeo

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