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. 2022 Nov 25;11(12):1697.
doi: 10.3390/antibiotics11121697.

Molecular Epidemiology of Carbapenem-Resistant K. pneumoniae Clinical Isolates from the Adult Patients with Comorbidities in a Tertiary Hospital, Southern Saudi Arabia

Affiliations

Molecular Epidemiology of Carbapenem-Resistant K. pneumoniae Clinical Isolates from the Adult Patients with Comorbidities in a Tertiary Hospital, Southern Saudi Arabia

Abdullah M Alshahrani et al. Antibiotics (Basel). .

Abstract

Hospitalized patients are likely to have chronic illnesses and are at an increased risk of mortality due to infection caused by MDR bacteria. We aimed to identify carbapenem-resistant genes carrying Klebsiella pneumoniae (K. pneumoniae) isolates and their risk factors recovered from adult patients with comorbidities. A cross-sectional study was carried out between April 2021 and December 2021 at King Abdullah Hospital (KAH) in Bisha province, Saudi Arabia. Seventy-one multi-drug resistant K. pneumoniae recovered from clinical samples and screened for carbapenemase genes of blaOXA-48-like, blaNDM-1, blaKPC, blaVIM, and blaIMP. Of 71 MDR K. pneumoniae examined, 47 (66.2%) isolates harbored various carbapenemase genes. The most prevalent single resistance gene was blaOXA-48-like (62.5%; n = 25), and 33.3% of them were recovered from sputum isolates. The blaNDM-1 gene was detected in 12 (30.0%) isolates, and eight of them were recovered from urine (n = 4) and blood (n = 4). Two (5.0%) single blaKPC genes were recovered from the sputum (n = 1) and blood (n = 1) isolates. In contrast, no blaIMP- and blaVIM-carrying isolates were detected. The co-existence of two resistance genes between blaOXA-48-like and blaNDM-1 was found in six strains, whereas only one strain was found to be produced in the three genes of blaNDM-1, blaKPC, and blaOXA-48-like. There were statistically significant associations between the presence of carbapenem-gene-carrying K. pneumoniae and patients' gender (χ2(1) = 5.94, p = 0.015), intensive care unit admission (χ2(1) = 7.649, p = 0.002), and chronic obstructive pulmonary disease (χ2(1) = 4.851, p = 0.028). The study highlighted the existence of carbapenemase-producing K. pneumoniae, particularly blaOXA-48-like and blaNDM-1, in patients with comorbidities. Our findings emphasize the importance of the molecular characterization of resistance-determinant-carrying bacterial pathogens as a part of infection control and prevention in hospital settings.

Keywords: Klebsiella pneumoniae; Saudi Arabia; carbapenemase genes; comorbidities.

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Conflict of interest statement

The authors state that they have no competing interests.

Figures

Figure 1
Figure 1
Results of multiplex PCR amplification of genes in MDR Klebsiella pneumoniae: (A) Lane 1, 2, 4 showed blaOXA-48-like (281 bp) expression; Lane 3, 5, 6, 7 showed negative results. (B) lane 1, 3, 5, 7 showed blaOXA-48-like (281bp) expression; Lane 2, 4, 6 were negative. (C) Lane 3 and 7 showed blaKPC (538 bp) expression; Lane 1, 2, 4, 5, 6 were negative. (D) Lane 4 showed blaNDM-1 (621 bp) expression; Lane 1, 2, 3, 5, 6, 7 were negative.
Figure 2
Figure 2
Distribution of carbapenemase-producing MDR. Klebsiella pneumoniae based on the types of clinical specimens.
Figure 3
Figure 3
Distribution of carbapenemase-producing MDR. Klebsiella pneumoniae among hospital wards.

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