An extensively drug-resistant Pseudomonas aeruginosa isolate from Myanmar.
AMR abbreviation: Aph, aminoglycoside phosphotransferase
Aac, aminoglycoside acetyltransferase
AadA, aminoglycoside adenylyltransferase
CrpP, ciprofloxacin resistance protein
ParRS, topoisomerase
beta-lactamase resistance genes (bla(PAO), and bla(OXA))
blaIMP, imipenamase
chloramphenicol acetyltransferase (catB7) and Sul, sulfonamide resistant
gyrA, DNA gyrase
Journal
Journal of global antimicrobial resistance
ISSN: 2213-7173
Titre abrégé: J Glob Antimicrob Resist
Pays: Netherlands
ID NLM: 101622459
Informations de publication
Date de publication:
20 Nov 2023
20 Nov 2023
Historique:
received:
21
08
2023
revised:
18
10
2023
accepted:
13
11
2023
medline:
23
11
2023
pubmed:
23
11
2023
entrez:
22
11
2023
Statut:
aheadofprint
Résumé
Antimicrobial resistance (AMR) including multidrug-resistant (MDR) and extensively drug-resistant (XDR) Pseudomonas aeruginosa has emerged as one of the serious public health threats across the globe. Southeast Asia is a 'hot spot' of antimicrobial-resistant bacteria including MDR P. aeruginosa. Despite Myanmar being located in Southeast Asia and suffering from a high infectious disease burden, data on MDR and XDR P. aeruginosa from Myanmar is limited. In this communication, we report the draft genome of an XDR P. aeruginosa isolate, MMXDRPA001 that was identified during a routine diagnosis in Myanmar. An MMXDRPA001 isolate colonising a hospitalised patient was characterised by antibiotic resistance profiling following standard methods and whole-genome sequencing using an Illumina MiSeq platform. The generated reads were de novo assembled using SPAdes (v.3.9.1). Annotation was performed by Prokka (v.1.14.0). Sequence type, antimicrobial resistance and virulence-related genes were predicted from the sequence. The phylogenetic relationships of all P. aeruginosa isolates were determined using core genome single nucleotide polymorphisms (SNPs) analysis utilising Snippy (v.4.6.0) and Gubbins (v.2.3.4). P. aeruginosa MMXDRPA001 was resistant to most antipseudomonal β-lactams, aminoglycosides and quinolones. The assembly comprised 145 contigs totalling 6,808,493 bases of sequence and a total of 6,183 coding sequences. The isolate belonged to sequence type (ST) 235, contained carbapenemase-encoding gene bla The identification of an international high-risk clone of ST235 XDR isolate in Myanmar, genomically relating to that from a neighbouring country underscores the need for coordinated AMR surveillance throughout healthcare settings in Myanmar and in the Southeast Asia region.
Identifiants
pubmed: 37992964
pii: S2213-7165(23)00199-6
doi: 10.1016/j.jgar.2023.11.004
pii:
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Informations de copyright
Copyright © 2023. Published by Elsevier Ltd.