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Published on: February 23, 2014
Virulence factors and clinical patterns of multiple-clone hypermucoviscous KPC-2 producing K. pneumoniae
J M Vargas1, M P Moreno Mochi1, J M Nuñez2
1Universidad Nacional de Tucumán, Facultad de Bioquímica, Química y Farmacia, Instituto de Microbiología Luis C. Verna, Cátedra de Bacteriología, Laboratorio de Antimicrobianos, Ayacucho 471, CP:4000, San Miguel de Tucumán, Tucumán, Argentina.
Abstract:
Carbapenemase-producing Klebsiella pneumoniae (CRKP) are increasingly reported worldwide being necessary the local epidemiological monitoring. Our aim was to characterize the hypermucoviscous CRKP isolates collected in our hospital during a 6 months period. Carriage of the carbapenemase genes (bla KPC, bla NDM, bla VIM and bla OXA-48), extended spectrum β-lactamases (bla SHV-2, bla CTX-M) and the virulence genes (magA, k2A, rmpA, wabG, uge, allS, entB, ycfM, kpn, wcaG, fimH, mrkD, iutA, iroN, hly and cnf-1) were determined by multiplex-PCR. Genetic relationship among the isolates was performed by PFGE and MLST. A total of 35 isolates were recovered, being the urinary and respiratory tract the most common infection sites (34.2%). The bla KPC-2 gene was present in all the isolates, coexisting with bla CTX-M-2 (45.7%), bla SHV-2 (28.6%), and bla CTX-M-2/bla SHV-2 (14.3%). The capsular serotype K2 corresponded with 68.6% of the isolates. Virulence factors frequency were variable [adhesins (97.1%), siderophores (94.3%) and phagocytosis resistance (wabG 48.5%, uge 80% and ycfM 57.1%)]. A total of 10 STs were identified although 40% of them clustered on ST25-CC65, and 17% to ST17. The incidence of KPC-2-producing K. pneumoniae reported by the hospital was 0.290 per 1000 admissions. In summary we described an epidemic scenario of multidrug resistant hypermucoviscous KPC-2 producing ST25 K. pneumoniae in our institution.
Insights
Hypermucoviscous carbapenemase-producing Klebsiella pneumoniae (CRKP) isolates, primarily KPC-2 positive and serotype K2, were characterized. ST25-CC65 was identified as a dominant multidrug-resistant clone in this hospital outbreak.
Area of Science:
- Microbiology
- Infectious Diseases
- Genetics
Background:
- Carbapenemase-producing Klebsiella pneumoniae (CRKP) poses a significant global health threat.
- Local epidemiological monitoring is crucial for managing CRKP outbreaks.
- Hypermucoviscous strains of CRKP are associated with increased virulence.
Purpose of the Study:
- To characterize hypermucoviscous CRKP isolates from a hospital setting over six months.
- To identify carbapenemase, extended-spectrum β-lactamase, and virulence genes.
- To determine the genetic relatedness and prevalent sequence types (STs) among isolates.
Main Methods:
- Multiplex-PCR was used to detect carbapenemase and virulence genes.
- Pulsed-field gel electrophoresis (PFGE) and multilocus sequence typing (MLST) were employed for genetic analysis.
- Isolates were collected from clinical samples over a 6-month period.
Main Results:
- All 35 CRKP isolates harbored the blaKPC-2 gene, often co-occurring with blaCTX-M-2 and/or blaSHV-2.
- The capsular serotype K2 was predominant (68.6%).
- Common virulence factors included adhesins (97.1%) and siderophores (94.3%).
- Ten STs were identified, with ST25-CC65 (40%) and ST17 (17%) being the most frequent.
- The incidence of KPC-2-producing K. pneumoniae was 0.290 per 1000 admissions.
Conclusions:
- A multidrug-resistant, hypermucoviscous KPC-2 producing ST25 K. pneumoniae clone caused an epidemic in the institution.
- The findings highlight the importance of continuous surveillance for CRKP.
- Understanding the genetic and virulence profiles of CRKP is essential for effective control strategies.
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