RES-Xre toxin-antitoxin locus knaAT maintains the stability of the virulence plasmid in Klebsiella pneumoniae
Hypervirulent isolates have been increasingly reported worldwide especially hypervirulent drug-resistant variants owing to the acquisition of a mobilizable virulence plasmid by a carbapenem-resistant strain. This pLVPK-like mobilizable plasmid encodes various virulence factors; however, information...
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Veröffentlicht in: | Emerging microbes & infections 2024-12, Vol.13 (1), p.2316814-2316814 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Hypervirulent
isolates have been increasingly reported worldwide
especially hypervirulent drug-resistant variants owing to the acquisition of a mobilizable virulence plasmid by a carbapenem-resistant strain. This pLVPK-like mobilizable plasmid encodes various virulence factors; however, information about its genetic stability is lacking. This study aimed to investigate the type II toxin-antitoxin (TA) modules that facilitate the virulence plasmid to remain stable in
. More than 3,000 TA loci in 2,000
plasmids were examined for their relationship with plasmid cargo genes. TA loci from the RES-Xre family were highly correlated with virulence plasmids of hypervirulent
. Overexpression of the RES toxin KnaT, encoded by the virulence plasmid-carrying RES-Xre locus
halts the cell growth of
and
, whereas co-expression of the cognate Xre antitoxin KnaA neutralizes the toxicity of KnaT.
and
were co-transcribed, representing the characteristics of a type II TA module. The
deletion mutation gradually lost its virulence plasmid in
whereas the stability of the plasmid in
was enhanced by adding
, which revealed that the
operon maintained the genetic stability of the large virulence plasmid in
. String tests and mouse lethality assays subsequently confirmed that a loss of the virulence plasmid resulted in reduced pathogenicity of
. These findings provide important insights into the role of the RES-Xre TA pair in stabilizing virulence plasmids and disseminating virulence genes in
e. |
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ISSN: | 2222-1751 2222-1751 |
DOI: | 10.1080/22221751.2024.2316814 |