Main content area

Nosocomial Outbreak of VIM-1-Producing Klebsiella pneumoniae Isolates of Multilocus Sequence Type 15: Molecular Basis, Clinical Risk Factors, and Outcome

Sánchez-Romero, Isabel, Asensio, Ángel, Oteo, Jesús, Muñoz-Algarra, María, Isidoro, Beatriz, Vindel, Ana, Álvarez-Avello, José, Balandín-Moreno, Bárbara, Cuevas, Oscar, Fernández-Romero, Sara, Azañedo, Luisa, Sáez, David, Campos, José
Antimicrobial agents and chemotherapy 2012 v.56 no.1 pp. 420-427
Klebsiella pneumoniae, antibiotic resistance, bacterial infections, behavior change, beta-lactamase, case-control studies, cephalosporins, cross infection, genes, human resources, molecular epidemiology, mortality, multilocus sequence typing, parenteral feeding, patients, plasmids, polymerase chain reaction, pulsed-field gel electrophoresis, replicon, risk factors
We study the epidemiology, molecular basis, clinical risk factors, and outcome involved in the clonal dissemination of VIM-1-producing Klebsiella pneumoniae isolates in the hospital setting. All patients infected/colonized by carbapenem-nonsusceptible K. pneumoniae (CNSKP) in 2009 were included. Molecular epidemiology was studied by pulsed-field gel electrophoresis (PFGE) and multilocus sequence typing (MLST). Antibiotic resistance genes were analyzed by PCR and sequencing. Plasmids were studied by PFGE with S1 nuclease digestion and for incompatibility group by a PCR-based replicon typing scheme. Risk factors associated with CNSKP colonization/infection were assessed by an observational case-control study. All 55 patients studied were infected (n = 28) or colonized (n = 27) by VIM-1-producing K. pneumoniae. All but one acquired isolates of a single clone (PFGE cluster 1 [C1], sequence type 15 [ST15]), while another clone (PFGE C2, ST340) was detected in four patients. C1 isolates also produced the new extended-spectrum β-lactamase SHV-134. blaVIM-1 was carried in a class 1 integron and an untypeable plasmid of ∼50 bp. The number of days that the patient received mechanical ventilation, the use of parenteral nutrition, previous treatment with linezolid, and treatment with extended-spectrum cephalosporins for more than 7 days were detected to be independent risk factors for CNSKP acquisition. The VIM-1-producing K. pneumoniae ST15 clone has a high capacity to spread among intensive care unit patients with severe underlying conditions. A high rate of associated mortality and great difficulty in controlling the spread of this clone, without permanent behavioral changes in the personnel, were observed.