Repatriation of a patient with COVID-19 contributed to the importation of an emerging carbapenemase producer
Options
BORIS DOI
Date of Publication
December 2021
Publication Type
Article
Contributor
Series
Journal of global antimicrobial resistance
ISSN or ISBN (if monograph)
2213-7165
Publisher
Elsevier
Language
English
Publisher DOI
PubMed ID
34718203
Uncontrolled Keywords
Description
BACKGROUND
Patients hospitalized abroad can become colonized with multidrug-resistant bacteria and import them to their home countries. In this work, we characterized an OXA-484 carbapenemase-producing Escherichia coli strain from a Swiss patient infected by SARS-CoV-2 and repatriated from India.
METHODS
At admission to Switzerland (April, 2021), the patient undertook a molecular nasopharyngeal swab to search for SARS-CoV-2 and a rectal swab to detect multidrug-resistant bacteria. Both SARS-CoV-2 and E. coli isolates were whole-genome sequenced and analyzed for phylogenetic relatedness.
RESULTS
The patient was infected with the SARS-CoV-2 B.1.617.2 lineage (VOC Delta), a lineage that started to be reported across Switzerland at that time. He was also colonized with a sequence type (ST) 410 E. coli strain (L3452210II) producing the OXA-484, a single amino acid variant of OXA-181. The blaOXA-484 was carried by a 51.5 kb IncX3 plasmid identical to those described in blaOXA-181-harboring ST410 E. coli strains. Core-genome analysis showed that L3452210II was identical (∆SNV ≤23) to two ST410 OXA-484 producers recently reported in Qatar and Germany, but differed from other ST410 OXA-181 producers reported worldwide.
CONCLUSIONS
The patient was infected by an emerging SARS-CoV-2 variant, and also imported an E.coli producing OXA-484, an OXA-48-like carbapenemase not yet reported in Switzerland. The genetic background of L3452210II indicated that the blaOXA-484 shared the same plasmid of blaOXA-181, but its bacterial host differed from most of the pandemic OXA-181-producing ST410 strains previously reported. This case description underlines that the COVID-19 crisis can contribute to the worldwide spread of emerging carbapenemase producers.
Patients hospitalized abroad can become colonized with multidrug-resistant bacteria and import them to their home countries. In this work, we characterized an OXA-484 carbapenemase-producing Escherichia coli strain from a Swiss patient infected by SARS-CoV-2 and repatriated from India.
METHODS
At admission to Switzerland (April, 2021), the patient undertook a molecular nasopharyngeal swab to search for SARS-CoV-2 and a rectal swab to detect multidrug-resistant bacteria. Both SARS-CoV-2 and E. coli isolates were whole-genome sequenced and analyzed for phylogenetic relatedness.
RESULTS
The patient was infected with the SARS-CoV-2 B.1.617.2 lineage (VOC Delta), a lineage that started to be reported across Switzerland at that time. He was also colonized with a sequence type (ST) 410 E. coli strain (L3452210II) producing the OXA-484, a single amino acid variant of OXA-181. The blaOXA-484 was carried by a 51.5 kb IncX3 plasmid identical to those described in blaOXA-181-harboring ST410 E. coli strains. Core-genome analysis showed that L3452210II was identical (∆SNV ≤23) to two ST410 OXA-484 producers recently reported in Qatar and Germany, but differed from other ST410 OXA-181 producers reported worldwide.
CONCLUSIONS
The patient was infected by an emerging SARS-CoV-2 variant, and also imported an E.coli producing OXA-484, an OXA-48-like carbapenemase not yet reported in Switzerland. The genetic background of L3452210II indicated that the blaOXA-484 shared the same plasmid of blaOXA-181, but its bacterial host differed from most of the pandemic OXA-181-producing ST410 strains previously reported. This case description underlines that the COVID-19 crisis can contribute to the worldwide spread of emerging carbapenemase producers.
File(s)
| File | File Type | Format | Size | License | Publisher/Copright statement | Content | |
|---|---|---|---|---|---|---|---|
| JGAR-S-21-00589.pdf | text | Adobe PDF | 2.47 MB | publisher | accepted | ||
| 1-s2.0-S2213716521002307-main.pdf | text | Adobe PDF | 2.09 MB | Attribution-NonCommercial-NoDerivatives (CC BY-NC-ND 4.0) | published |