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Turton, J. F.

Publications and source records attributed to Turton, J. F..

2 recordsLinked to original sources

Long read sequencing provides an insight into plasmids found among carbapenemase producing Enterobacterales from hospitals in the United Kingdom during 2021 to 2023

107 isolates of Enterobacterales consisting of Klebsiella pneumoniae (n=90), Escherichia coli (n=7), Enterobacter cloacae complex (n=6), Klebsiella oxytoca complex (n=3) and Citrobacter freundi (n=1) and additionally an isolate of Acinetobacter baumannii carrying genes encoding NDM (NDM-1, NDM-5 and NDM-14), KPC (KPC-2 and KPC-3), OXA-48-like (OXA-48, OXA-181 and OXA-232) and IMP (IMP-1 and IMP-4) carbapenemases were sequenced using q20 nanopore chemistry to provide complete/near-complete assemblies and relevant plasmids compared. Investigation of potential plasmid outbreaks in individual hospitals among isolates of different types and species revealed a mixed situation with some isolates carrying similar plasmids, but with segments missing/added and some plasmids that were clearly distinct. While most plasmids carrying blaOXA-48 were typical IncL plasmids of approximately 60 kb that are widely described, there was some variation among these. One isolate carried an IncR plasmid that had only limited homology with the others. Identical 51,479 bp ColKP3/IncX3 plasmids carrying blaOXA-181 were found from isolates from different hospitals that exactly matched those on GenBank from other countries. In other isolates blaOXA-181 was carried on IncFII plasmids. blaOXA-232 was found in highly conserved small ColKP3 plasmids that matched those found in other countries and continents. These observations highlight the importance of understanding the wider distribution of plasmids of concern. IncHI2/IncHI2A plasmids were important vehicles for carbapenemase genes and were found with blaKPC-2, blaIMP-1, blaIMP-4 or blaNDM-1, sometimes with the colistin resistance gene mcr-9 in addition. Representatives of K. pneumoniae sequence type (ST) 147 from seven hospitals carried IncFIB(pNDM-Mar)/IncHI1B(pNDM-MAR) hybrid virulence resistance plasmids of 325 to 352 kb that combined blaNDM-5 and other resistance genes with genes found in virulence plasmids. A similar plasmid was also found in an isolate of K. pneumoniae ST1558 and has been described in representatives of ST383. Nanopore sequencing has been instrumental in improving our knowledge of plasmids carrying carbapenemase genes leading to a better understanding of their epidemiology.

microbiology↗

Virulence factors among isolates of extraintestinal Esherichia coli (ExPEC) from hospitals in the United Kingdom.

182 genes associated with virulence were sought from the whole genome sequences of all non-duplicate isolates of Escherichia coli received by the UK Health Security Agencys Antimicrobial Resistance and HealthCare Associated Infections laboratory for typing between June 2019 and March 2021 from hospitals in the United Kingdom and Republic of Ireland (n=593). These were from healthcare associated investigations and were not associated with diarrhoeal disease. Genes that were very common or very rare were excluded from further analysis. The frequency of detection of genes was compared among isolates from invasive infection, screening, urine samples and from neonates. cnf1 (coding for cytotoxic necrotising factor), clbK (coding for colibactin), focCDF (coding for F1 fimbriae), kpsM_K1, neuBD (associated with the K1 capsule), mchBC, mcmA (coding for microcins), papG_alleleIII (part of a cluster encoding P fimbriae), pic (protein involved in intestinal colonization), sfaE/sfafoCDE (coding for S fimbriae), tcpC (encoding TLR domain containing-protein C) and vat (encoding toxin vacuolating autotransporter) were 4 to 28 times more prevalent among isolates from invasive infections than among those from carriage. Representatives of sequence types (ST) 12, 73, 998 and 127 carried multiple of these virulence factors, no matter whether they were from screening swabs or from blood or other infection sites. Isolates carrying multiple virulence factors were more prevalent from neonatal screens than those from general screens. Genes associated with the K1 capsule (ibeA, neuBD, kpsM_K1) were particularly found in STs 1193, 10, 998, 538, 80 and 141. Nanopore sequencing of 14 isolates representing 10 different STs showed that the virulence elements sought were largely carried in chromosomal genomic islands, which were mosaic in nature. Some 9 % of isolates carried more than six of the main virulence genes/gene sets sought, highlighting the potential for significant numbers of carriage isolates to cause extraintestinal infections.

microbiology↗