2020
DOI: 10.3389/fcimb.2020.00054
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Antibiotic Resistance Profile, Outer Membrane Proteins, Virulence Factors and Genome Sequence Analysis Reveal Clinical Isolates of Enterobacter Are Potential Pathogens Compared to Environmental Isolates

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Cited by 27 publications
(20 citation statements)
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“…It would be expected there would be more and/or more potent virulence factors from clinical isolates compared to environmental isolates. For example, as corroborated by whole genome sequencing, in a recent study, it was suggested that there was limited pathogenic potential of environmental Enterobacter species isolates compared to clinical isolates (Mishra et al 2020). In our study, the only difference between the three clinical isolates and the two environmental isolates was that environmental isolate CGG3 does not have siderophores.…”
Section: Putative Virulence Factorssupporting
confidence: 61%
“…It would be expected there would be more and/or more potent virulence factors from clinical isolates compared to environmental isolates. For example, as corroborated by whole genome sequencing, in a recent study, it was suggested that there was limited pathogenic potential of environmental Enterobacter species isolates compared to clinical isolates (Mishra et al 2020). In our study, the only difference between the three clinical isolates and the two environmental isolates was that environmental isolate CGG3 does not have siderophores.…”
Section: Putative Virulence Factorssupporting
confidence: 61%
“…This explains why ESR systems are involved or contribute in the sensing and transmission of internal signal that activate the genetic cascades controlling the envelope permeability and transports. Consequently, the TCS systems have been proposed as new target for original antibacterial agents in order to impair the bacterial adaptation and virulence [ 86 , 119 , 133 , 134 , 135 ]. In the same way, targeting sRNAs is currently being considered in view of their central implication in the regulatory network leading to antibiotic resistance [ 88 , 90 ].…”
Section: Discussionmentioning
confidence: 99%
“…In Gram-negative bacteria, the production of chromosomal AmpC enzymes was lower compared to plasmid-encoded AmpC enzymes; however, this product can be enhanced by the induction of some β-lactams, such as cefoxitin. E. coli and K. pneumoniae strains harbouring AmpC β-lactamases have the ability to lose porin Omp-K35 from their outer membrane and show resistance against cephamycin because this porin permits water soluble β-lactams to passthrough and gain access into the cells [63]. Recent studies found that more than twenty plasmid-expressed AmpC β-lactamases exist.…”
Section: Ampc β-Lactamasesmentioning
confidence: 99%