Comparison of factors contributing to drug resistance and infection severity in Pseudomonas aeruginosa isolates among COVID-19 and non-COVID-19 patients.

Publication date: Jun 23, 2025

SARS-CoVs increase susceptibility to bacterial co-infections, with Pseudomonas aeruginosa frequently detected in COVID-19 patients. Factors such as drug resistance, mobile genetic elements, and biofilm formation further complicate these infections. This study compared these characteristics in P. aeruginosa isolates from COVID-19 and non-COVID-19 patients. During a one-year study, 125 P. aeruginosa isolates were collected from COVID-19 patients (37 isolates) and non-COVID-19 patients (88 isolates). They were identified using conventional microbiological methods. Antimicrobial resistance patterns and multidrug-resistant (MDR) isolates were determined according to CLSI guidelines and MDR definitions. Biofilm formation was evaluated using a microtiter plate assay, and the presence of genes related to plasmid-mediated quinolone resistance (PMQR), integrons, and biofilm formation was determined by polymerase chain reaction (PCR). The highest resistance and susceptibility among the COVID-19 and non-COVID-19 groups were observed with imipenem (51. 4% vs. 42%) and cefepime (73% vs. 64. 8%), respectively. Quinolones resistance ranged from 32 to 36%. Overall, 54 isolates (43. 2%) were MDR, with colistin resistance found in 50% and 37. 5% of MDR isolates from COVID-19 and non-COVID-19 patients, respectively. Isolates from COVID-19 patients also showed stronger biofilm-forming ability. Among PMQR genes, only aac(6′)-Ib-cr was detected (47. 2% of isolates). The prevalence of aac(6′)-Ib-cr, class 1 integron, and pelF genes was significantly higher in isolates from COVID-19 patients. Resistance to commonly used antibiotics from different classes, along with biofilm formation, class 1 integron, aac(6′)-Ib-cr, and biofilm-associated genes, were higher in COVID-19 isolates, likely contributed to the greater severity of infections in this group.

Concepts Keywords
Antibiotics Anti-Bacterial Agents
Genetic Anti-Bacterial Agents
Pcr Biofilm
Polymerase Biofilms
Coinfection
COVID-19
COVID-19
Female
Humans
Integron
Integrons
Male
Microbial Sensitivity Tests
Middle Aged
Plasmids
PMQR
Pseudomonas aeruginosa
Pseudomonas aeruginosa
Pseudomonas Infections
Quinolones
Quinolones
SARS-CoV-2

Semantics

Type Source Name
disease MESH infection
disease MESH COVID-19
disease IDO susceptibility
disease MESH co-infections
pathway KEGG Biofilm formation
disease IDO assay
drug DRUGBANK Imipenem
drug DRUGBANK Cefepime
drug DRUGBANK Colistin
disease MESH Long Covid
disease MESH Pseudomonas Infections

Original Article

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