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Published on: February 1, 2014
First report of KPC-35-producing Klebsiella pneumoniae ST258 isolated in Peru
Arturo Gonzales-Rodriguez1, Juan Carlos Gómez-de-la-Torre2, Luis Alvarado2
1Universidad de Piura, Facultad de Medicina Humana, Lima, Peru.
Abstract:
Klebsiella pneumoniae sequence type 258 (ST258) is the main cause of the global spread of KPC and a significant public health problem. In 2015, ceftazidime/avibactam (CZA) was introduced as a therapeutic alternative and since it has contributed to the development of new KPC variants. Here we present the identification of two consecutive isolations of K. pneumoniae ST258 (KP1 and KP2), from a patient with urinary tract infection. KP1 and KP2 harbored blaKPC-2 and blaKPC-35, respectively. KP2 exhibited a modified susceptibility profile to carbapenems and resistance to CZA. To the best of our knowledge, this is the first report of K. pneumoniae ST258 in Peru, which highlights the increasing problem of CZA resistance.
Insights
The emergence of Klebsiella pneumoniae ST258 with new KPC variants, including ceftazidime/avibactam resistance, poses a significant public health threat. This study reports the first cases in Peru, highlighting the urgent need for surveillance and new treatment strategies.
Area of Science:
- Microbiology
- Infectious Diseases
- Antimicrobial Resistance
Background:
- Klebsiella pneumoniae sequence type 258 (ST258) is a major driver of carbapenemase-producing Enterobacteriaceae (KPC) infections globally.
- Ceftazidime/avibactam (CZA) was introduced in 2015 as a treatment option for KPC infections, but resistance has since emerged.
- The spread of KPC-producing bacteria, particularly ST258, represents a critical public health challenge.
Purpose of the Study:
- To report the identification of K. pneumoniae ST258 isolates from a patient in Peru.
- To characterize the antimicrobial resistance profiles, including resistance to CZA, of these isolates.
- To highlight the emergence of CZA resistance in K. pneumoniae ST258 in a new geographical region.
Main Methods:
- Isolation and identification of K. pneumoniae from patient samples.
- Antimicrobial susceptibility testing, including carbapenems and CZA.
- Molecular characterization of resistance genes, specifically blaKPC variants.
Main Results:
- Two consecutive K. pneumoniae ST258 isolates (KP1 and KP2) were identified from a urinary tract infection patient.
- KP1 harbored blaKPC-2, while KP2 harbored blaKPC-35.
- KP2 displayed reduced susceptibility to carbapenems and confirmed resistance to CZA.
- This represents the first report of K. pneumoniae ST258 in Peru.
Conclusions:
- The findings underscore the increasing global challenge of CZA resistance in K. pneumoniae ST258.
- The emergence of CZA-resistant K. pneumoniae ST258 in Peru necessitates enhanced surveillance and infection control measures.
- Continuous monitoring for emerging resistance mechanisms is crucial for effective antimicrobial stewardship.
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