TY - JOUR
T1 - Dominance of Escherichia coli sequence types ST73, ST95, ST127 and ST131 in Australian urine isolates
T2 - A genomic analysis of antimicrobial resistance and virulence linked to F plasmids
AU - Li, Dmitriy
AU - Elankumaran, Paarthiphan
AU - Kudinha, Timothy
AU - Kidsley, Amanda K.
AU - Trott, Darren J.
AU - Jarocki, Veronica Maria
AU - Djordjevic, Steven Philip
N1 - Publisher Copyright:
© 2023 The Authors.
PY - 2023/7/1
Y1 - 2023/7/1
N2 - Extraintestinal pathogenic Escherichia coli (ExPEC) are the most frequent cause of urinary tract infections (UTIs) globally. Most studies of clinical E. coli isolates are selected based on their antimicrobial resistance (AMR) phenotypes; however, this selection bias may not provide an accurate portrayal of which sequence types (STs) cause the most disease. Here, whole genome sequencing (WGS) was performed on 320 E. coli isolates from urine samples sourced from a regional hospital in Australia in 2006. Most isolates (91%) were sourced from patients with UTIs and were not selected based on any AMR phenotypes. No significant differences were observed in AMR and virulence genes profiles across age sex, and uro-clinical syndromes. While 88 STs were identified, ST73, ST95, ST127 and ST131 dominated. F virulence plasmids carrying senB-cjrABC (126/231; 55%) virulence genes were a feature of this collection. These senB-cjrABC+ plasmids were split into two categories: pUTI89-like (F29:A-:B10 and/or >95 % identity to pUTI89) (n=73) and non-pUTI89-like (n=53). Compared to all other plasmid replicons, isolates with pUTI89-like plasmids carried fewer antibiotic resistance genes (ARGs), whilst isolates with senB-cjrABC+/non-pUTI89 plasmids had a significantly higher load of ARGs and class 1 integrons. F plasmids were not detected in 89 genomes, predominantly ST73. Our phylogenomic analyses identified closely related isolates from the same patient associated with different pathologies and evidence of strain-sharing events involving isolates sourced from companion and wild animals.
AB - Extraintestinal pathogenic Escherichia coli (ExPEC) are the most frequent cause of urinary tract infections (UTIs) globally. Most studies of clinical E. coli isolates are selected based on their antimicrobial resistance (AMR) phenotypes; however, this selection bias may not provide an accurate portrayal of which sequence types (STs) cause the most disease. Here, whole genome sequencing (WGS) was performed on 320 E. coli isolates from urine samples sourced from a regional hospital in Australia in 2006. Most isolates (91%) were sourced from patients with UTIs and were not selected based on any AMR phenotypes. No significant differences were observed in AMR and virulence genes profiles across age sex, and uro-clinical syndromes. While 88 STs were identified, ST73, ST95, ST127 and ST131 dominated. F virulence plasmids carrying senB-cjrABC (126/231; 55%) virulence genes were a feature of this collection. These senB-cjrABC+ plasmids were split into two categories: pUTI89-like (F29:A-:B10 and/or >95 % identity to pUTI89) (n=73) and non-pUTI89-like (n=53). Compared to all other plasmid replicons, isolates with pUTI89-like plasmids carried fewer antibiotic resistance genes (ARGs), whilst isolates with senB-cjrABC+/non-pUTI89 plasmids had a significantly higher load of ARGs and class 1 integrons. F plasmids were not detected in 89 genomes, predominantly ST73. Our phylogenomic analyses identified closely related isolates from the same patient associated with different pathologies and evidence of strain-sharing events involving isolates sourced from companion and wild animals.
KW - Antimicrobial resistance
KW - ExPEC
KW - F plasmids
KW - pUTI89
KW - senB
KW - UTIs
UR - http://www.scopus.com/inward/record.url?scp=85165385078&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85165385078&partnerID=8YFLogxK
U2 - 10.1099/mgen.0.001068
DO - 10.1099/mgen.0.001068
M3 - Article
C2 - 37471138
AN - SCOPUS:85165385078
SN - 2057-5858
VL - 9
SP - 1
EP - 18
JO - Microbial Genomics
JF - Microbial Genomics
IS - 7
M1 - 001068
ER -