2019
DOI: 10.1016/j.jgar.2019.06.007
|View full text |Cite
|
Sign up to set email alerts
|

Genomic diversification of IncR plasmids from China

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

1
8
0

Year Published

2020
2020
2024
2024

Publication Types

Select...
9

Relationship

1
8

Authors

Journals

citations
Cited by 18 publications
(9 citation statements)
references
References 38 publications
1
8
0
Order By: Relevance
“…To date, multiple plasmids have been found to be the vesicles for spread of carbapenemase, ESBLs, and PMQRs [34]. The high prevalence of IncFII, IncR and IncFIB plasmid replicons in our study alert us on the urgency of implementing antimicrobial resistance surveillance, since IncFII-type plasmids are highly distributed vesicles for resistant determinants in Enterobacteriaceae [35]; Moreover, IncR plasmid is an important reservoir of multidrug resistance in Enterobacteriaceae strains, because the conserved IncR backbones include the multidrug resistant (MDR) regions [36]; and IncFIB plasmids were reported to be associated with majority of the antimicrobial resistance genes [37]. Similarly, some of the distribution correlations between various plasmid replicons and multiple resistant genes found in our study are consistent with the previous reports [38][39][40].…”
Section: Discussionmentioning
confidence: 67%
“…To date, multiple plasmids have been found to be the vesicles for spread of carbapenemase, ESBLs, and PMQRs [34]. The high prevalence of IncFII, IncR and IncFIB plasmid replicons in our study alert us on the urgency of implementing antimicrobial resistance surveillance, since IncFII-type plasmids are highly distributed vesicles for resistant determinants in Enterobacteriaceae [35]; Moreover, IncR plasmid is an important reservoir of multidrug resistance in Enterobacteriaceae strains, because the conserved IncR backbones include the multidrug resistant (MDR) regions [36]; and IncFIB plasmids were reported to be associated with majority of the antimicrobial resistance genes [37]. Similarly, some of the distribution correlations between various plasmid replicons and multiple resistant genes found in our study are consistent with the previous reports [38][39][40].…”
Section: Discussionmentioning
confidence: 67%
“…55,56 Furthermore, the IncR plasmid is a significant reservoir of many antibiotics resistance in Enterobacteriaceae isolates since the preserved IncR backbones contain the multidrug resistant (MDR) sequences. 57 Furthermore, IncFIIk plasmids were described to be related to the mainstream of the antimicrobial resistance genes detected more frequently in our study. 58 The extension of ST11 for the bla KPC-2 carrying K. pneumoniae was in the union as according to the earlier articles representing that, ST11 is the main epidemic clone among K. pneumonia.…”
Section: Discussionmentioning
confidence: 58%
“…qnr genes have been previously associated with IncN plasmids from different Salmonella serovars isolated from human and poultry samples in the Netherlands (García-Fernández et al, 2009). It has been shown previously that IncR plasmids are able to form multireplicons with IncN, IncA/C, IncHI, and IncF type plasmids (Drieux et al, 2013;Jing et al, 2019;Papagiannitsis et al, 2013;Qu et al, 2019). Previous studies indicate that IncR plasmids lack genes involved in conjugation (Bielak et al, 2011;Chen et al, 2006), which indicates that pZPK-H11 is a putatively conjugative plasmid contributing to the transferassociated genes located on the IncN region of the plasmid.…”
Section: Discussionmentioning
confidence: 99%
“…Bacterial multilocus sequence typing (MLST) was determined with MLST 2.0 (Larsen et al, 2012) using E. coli scheme 1 (Wirth et al, 2006). Virulence genes for E. coli isolates were determined with VirulenceFinder 2.0 (Joensen et al, 2014), using an identity threshold of 90% and a minimum length of 60%. PlasmidFinder 2.1 (Carattoli et al, 2014) was used to determine plasmid replicons located in the same contigs as beta-lactamase genes using an identity threshold of 95% and a minimum length of 60%.…”
Section: Bioinformatic Analysesmentioning
confidence: 99%