Virulent and multidrug-resistant Klebsiella pneumoniae from clinical samples in Balochistan.
Sareeen FatimaFaiza LiaqatAli AkbarMuhammad SahfeeAbdul SamadMuhammad AnwarShazia IqbalShabir Ahmad KhanHaleema SadiaGul MakaiAnila BahadurWajeeha NaeemAdnan KhanPublished in: International wound journal (2021)
Klebsiella pneumoniae is an important pathogen causing hospital-acquired infections in human beings. Samples from suspected patients of K pneumoniae associated with respiratory and urinary tract infections were collected at Bolan Medical Complex, Quetta, Balochistan. Clinical samples (n = 107) of urine and sputum were collected and processed for K pneumoniae isolation using selective culture media. Initially, 30 of 107 isolates resembling Klebsiella spp. were processed for biochemical profiling and molecular detection using gyrase A (gyrA) gene for conformation. The K pneumoniae isolates were analysed for the presence of drug resistance and virulence genes in their genomes. The 21 of 107 (19.6%) isolates were finally confirmed as K pneumoniae pathogens. An antibiogram study conducted against 17 different antibiotics showed that a majority of the isolates are multidrug resistant. All the isolates (100%) were resistant to amoxicillin, cefixime, amoxicillin-clavulanic acid, cefotaxime, and ceftriaxone followed by tetracycline (95.2%), ciprofloxacin and gentamicin (76.2%), sulphamethoxazol (66.7%), nalidixic acid (61.9%), norfloxacine (42.9%), piperacillin-tazobactam (23.8%), cefoperazone-sulbactam (19%), and cefotaxime-clavulanic acid (33.3%), whereas all the isolates showed sensitivity to amikacin, chloramphenicol, and imipenem. The presence of tetracycline, sulphamethoxazol-resistant genes, and extended-spectrum beta-lactamase was reconfirmed using different specific genes. The presence of virulence genes fimH1 and EntB responsible for adherence and enterobactin production was confirmed in the isolates. The high virulence and drug resistance potential of these Klebsiella isolates are of high public health concern. Multidrug resistance and virulence potential in K. pneumoniae are converting these nosocomial pathogens into superbugs and making its management harder.
Keyphrases
- klebsiella pneumoniae
- multidrug resistant
- escherichia coli
- gram negative
- genetic diversity
- acinetobacter baumannii
- pseudomonas aeruginosa
- drug resistant
- antimicrobial resistance
- public health
- genome wide
- staphylococcus aureus
- end stage renal disease
- biofilm formation
- urinary tract infection
- genome wide identification
- chronic kidney disease
- cystic fibrosis
- respiratory tract
- genome wide analysis
- emergency department
- metabolic syndrome
- peritoneal dialysis
- gene expression
- mycobacterium tuberculosis
- single cell
- type diabetes
- patient reported outcomes
- insulin resistance
- methicillin resistant staphylococcus aureus
- skeletal muscle
- weight loss
- drug induced