Genetic Analysis, Population Structure, and Characterisation of Multidrug-Resistant Klebsiella pneumoniae from the Al-Hofuf Region of Saudi Arabia

• Published in: Pathogens (Basel) Vol. 10; no. 9; p. 1097
• Main Authors: Badger-Emeka, Lorina I., Al-Sultan, Abdulrahman A., Bohol, Marie Fe F., Al-Anazi, Mashael R., Al-Qahtani, Ahmed A.
• Format: Journal Article
• Language: English
• Published: Basel MDPI AG 28.08.2021; MDPI
• Subjects: Antibiotics; Antiinfectives and antibacterials; antimicrobial; Antimicrobial agents; Automation; Bacteria; clonal; DNA sequencing; Drug resistance; Electrophoresis; Epidemics; extended-beta lactamase; Gel electrophoresis; Gene sequencing; Genes; Genetic analysis; High resistance; Hospitals; Klebsiella; Klebsiella pneumoniae; Laboratories; multidrug; Multidrug resistance; Nosocomial infections; Nucleotide sequence; Pathogens; Phenotypes; Pneumonia; Population genetics; Population structure; Public health; resistance; rRNA 16S; Surveillance; Saudi Arabia; England; United Kingdom > UK; France; United States > US
• ISSN: 2076-0817; 2076-0817
• DOI: 10.3390/pathogens10091097

Multidrug-resistant Klebsiella pneumoniae (MDR-KP) is a major public health problem that is globally associated with disease outbreaks and high mortality rates. As the world seeks solutions to such pathogens, global and regional surveillance is required. The aim of the present study was to examine the antimicrobial susceptibility pattern and clonal relatedness of Klebsiella pneumoniae isolates collected for a period of three years through pulse field gel electrophoresis (PFGE). Isolate IDs, antimicrobial assays, ESBL-production, and minimum inhibitory concentrations (MICs) were examined with the Vitek 2 Compact Automated System. IDs were confirmed by 16S rRNA gene sequencing, with the resulting sequences being deposited in NCBI databases. DNA was extracted and resistance genes were detected by PCR amplification with appropriate primers. Isolates were extensive (31%) and multidrug-resistant (65%). Pulsotype clusters grouped the isolates into 22 band profiles that showed no specific pattern with phenotypes. Of the isolates, 98% were ESBL-KP, 69% were carbapenem-resistant Enterobacteriaceae (CRE) strains, and 72.5% comprised the carriage of two MBLs (SIM and IMP). Integrons (ISAba1, ISAba2, and IS18) were detected in 69% of the MDR-KP. Additionally, OXA-23 was detected in 67% of the isolates. This study therefore demonstrates clonal diversity among clinical K. pneumoniae, confirming that this bacterium has access to an enormous pool of genes that confer high resistance-developing potential.