Open AccessMolecular characterization of KPC-2-producing Klebsiella pneumoniae ST258 isolated from bovine mastitis
Author(s) -
Jesús Silva-Sánchez,
Humberto Barrios-Camacho,
Emmanuel Hernández-Rodriguez,
Josefina Dúran-Bedolla,
Alejandro Sánchez-Pérez,
Luary C. Martínez-Chavarría,
Juan Xicohtencatl-Cortés,
Rigoberto HernándezCastro,
Ulises Garza–Ramos
Publication year - 2021
Publication title -
brazilian journal of microbiology
Language(s) - English
Resource type - Journals
eISSN - 1678-4405
pISSN - 1517-8382
DOI - 10.1007/s42770-021-00445-y
Subject(s) - klebsiella pneumoniae , microbiology and biotechnology , mastitis , biology , plasmid , multilocus sequence typing , virulence , pulsed field gel electrophoresis , multiple drug resistance , antibiotics , fimbria , virology , gene , escherichia coli , genetics , genotype
Bovine mastitis, an inflammation of the mammary gland of dairy cattle, is the most prevalent disease causing economically important losses, reduced milk production, early culling, veterinary expenses, and higher death rates. Bovine mastitis infections are the main cause for the use of antibiotics; however, the emergence of multidrug-resistant bacteria and the poor or nil response to antibiotics has become a critical global health problem. The goal of this study was the characterization of bacterial infections associated with clinical bovine mastitis. All the isolates were multidrug-resistant and were negative for the production of extended spectrum β-lactamases. However, all isolates were identified as carbapenemase-producing organisms by the Carba NP test. The carbapenemase identified was the product of the KPC-2 gene. The isolates were identified as Klebsiella pneumoniae and contained virulence genes for fimbriae, lipopolysaccharides, nitrogen starvation genes, and siderophores. Sixty-nine percent of the KPC-2-producing isolates had the same plasmid profile, although the genetic mobilization of resistance by bacterial conjugation was unsuccessful. The carbapenemase corresponded to the plasmid-borne KPC-2 gene identified by Southern blot hybridization. The assay showed a positive signal in the 90 kb (69% of the isolates), 165 kb (31% of the isolates), and 130 kb (6% of the isolates) plasmids. The IncFII y and IncFII k replicons were detected among these K. pneumoniae isolates. The PFGE and MLST analysis showed that all of the isolates are comprised by two clones (A and B) belonging to Sequence Type 258. This is the first report of K. pneumoniae producing carbapenemase KPC-2 isolated from bovine mastitis.