# Current pattern of antibiotic resistance and molecular characterization of virulence genes in Klebsiella pneumoniae obtained from urinary tract infection (UTIs) patients, Peshawar

**Authors:** Zeeshan Khan, Qaisar Ali, Sadiq Azam, Ibrar Khan, Jamila Javed, Noor Rehman, Mesaik M. Ahmed, Jalal Uddin, Ajmal Khan, Ahmed Al-Harrasi, Yung-Fu Chang, Yung-Fu Chang, Yung-Fu Chang

PMC · DOI: 10.1371/journal.pone.0319273 · PLOS One · 2025-04-10

## TL;DR

This study examines antibiotic resistance and virulence genes in Klebsiella pneumoniae from UTI patients in Peshawar, highlighting the growing threat of drug-resistant infections.

## Contribution

The study provides a detailed molecular characterization of virulence genes and antibiotic resistance patterns in clinical isolates of K. pneumoniae from UTIs in a specific hospital setting.

## Key findings

- K. pneumoniae showed high resistance to trimethoprim/Sulfamethoxazole and Colistin, with Tigecycline and Cefepime being the most effective antibiotics.
- The fimH virulence gene was most prevalent, and mutations were observed in fimH and papEF, but not in sat, afa, or vat.
- Significant associations between bacterial types were found, supporting the null hypothesis with p ≤ 0.05.

## Abstract

The current study investigates the prevalence of virulence genes obtained from clinical isolates of multidrug-resistant (MDR) Klebsiella pneumoniae at Khyber Teaching Hospital Peshawar, from October 2021 to January 2023. Upon proper consent, clinical samples of suspected UTIs patients were collected and inoculated on the nutrients agar media, McConkey agar media, and Cysteine Lysine Electrolyte Deficient (CLED) agar media followed by incubation at 37°C for 24 hrs. The phenotypic and genotypic identification were employed for the bacterial isolates. The phenotypic identification includes gram staining followed by the Analytical Profile Index (API 20E). A total of 215 (3.85%) positive isolates were found with the highest prevalence observed among the female patients (4.35%) followed by male (3.26%). The highest prevalence, constituting 52.55% (n = 113), was detected in the age group of 21-40 years, followed by 31.62% (n = 68) in the 41-60 age group. Additionally, 10.23% (n = 22), 3.25% (n = 7), and 2.32% (n = 5) of cases were identified in the age groups of 01-10 years, 11-20 years, and above 60 years, respectively. Among the total positive samples, 44.65% (n = 96) were collected from the Outpatient department (OPD), while inpatient department (IPD) cases contributed 55.35% (n = 119). The antibiotic susceptibility profile of K. pneumoniae showed significant resistance to trimethoprim/Sulfamethoxazole (93%) and Colistin (79.07%). Tigecycline emerged as the most effective antibiotic with a sensitivity rate of 90%, along with Cefepime at the same level. Minimum Inhibitory Concentration (MIC) values indicated higher resistance for CTX, MEM, CN, AK, DO, CIP, and SXT in K. pneumoniae-causing UTIs from KTH, Peshawar. Molecular characterization of virulence genes reveals the highest prevalence of fimH (80%) followed by SAT (65%), papEF (49%), afa (29%), and VAT (16%). The sequencing data of the virulence genes reveals mutations in fimH and papEF, while sat, afa and vat virulence genes showed no mutations. The Chi-square test indicated a significant association between the types of bacteria, supporting our null hypothesis with a significance level of p ≤  0.05. The current study’s finding is to evaluate the rise of antibiotic resistance in hospital settings, which highly demands the focus of health authorities and clinicians to manage the burden of the disease effectively.

## Linked entities

- **Genes:** fimH (minor component of type 1 fimbriae) [NCBI Gene 913676], SAT1 (spermidine/spermine N1-acetyltransferase 1) [NCBI Gene 6303], AFA (ankyloblepharon filiforme adnatum) [NCBI Gene 170], vat (VCP-like ATPase) [NCBI Gene 1442053]
- **Chemicals:** trimethoprim/Sulfamethoxazole (PubChem CID 358641), Colistin (PubChem CID 5311054), Tigecycline (PubChem CID 54686904), Cefepime (PubChem CID 5479537), CTX (PubChem CID 16133838), CN (PubChem CID 5975), AK (PubChem CID 4130575), CIP (PubChem CID 16211675), SXT (PubChem CID 358641)
- **Diseases:** urinary tract infection (MONDO:0005247)
- **Species:** Klebsiella pneumoniae (taxon 573)

## Full-text entities

- **Genes:** AFA (ankyloblepharon filiforme adnatum) [NCBI Gene 170], SAT1 (spermidine/spermine N1-acetyltransferase 1) [NCBI Gene 6303] {aka DC21, KFSD, KFSDX, SAT, SSAT, SSAT-1}
- **Diseases:** urinary tract infection (MESH:D014552), Klebsiella pneumoniae (MESH:D007710)
- **Species:** Homo sapiens (human, species) [taxon 9606], Klebsiella pneumoniae (species) [taxon 573]

## Full text

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## References

28 references — full list in the complete paper: https://tomesphere.com/paper/PMC11984708/full.md

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Source: https://tomesphere.com/paper/PMC11984708