Mostrar el registro sencillo del ítem
dc.contributor.author | Carvajal, Lina P. | |
dc.contributor.author | Rincon, Sandra | |
dc.contributor.author | Echeverri, Aura M. | |
dc.contributor.author | Porras, Jessica | |
dc.contributor.author | Rios, Rafael | |
dc.contributor.author | Ordoñez, Karen M. | |
dc.contributor.author | Seas Ramos, Carlos Rafael | |
dc.contributor.author | Gomez-Villegas, Sara I. | |
dc.contributor.author | Diaz, Lorena | |
dc.contributor.author | Arias, Cesar A. | |
dc.contributor.author | Reyes, Jinnethe | |
dc.date.accessioned | 2020-07-14T00:01:02Z | |
dc.date.available | 2020-07-14T00:01:02Z | |
dc.date.issued | 2020 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12866/8257 | |
dc.description.abstract | Cefazolin has become a prominent therapy for methicillin-susceptible Staphylococcus aureus (MSSA) infections. However, an important concern is the cefazolin inoculum effect (CzIE), a phenomenon mediated by staphylococcal β-lactamases. Four variants of staphylococcal β-lactamases have been described based on serological methodologies and limited sequence information. Here, we sought to reassess the classification of staphylococcal β-lactamases and their correlation with the CzIE. We included a large collection of 690 contemporary bloodstream MSSA isolates recovered from Latin America, a region with a high prevalence of the CzIE. We determined cefazolin MICs at standard and high inoculums by broth microdilution. Whole-genome sequencing was performed to classify the β-lactamase in each isolate based on the predicted full sequence of BlaZ. We used the classical schemes for β-lactamase classification and compared it to BlaZ allotypes found in unique sequences using the genomic information. Phylogenetic analyses were performed based on the BlaZ and core-genome sequences. The overall prevalence of the CzIE was 40%. Among 641 genomes, type C was the most predominant β-lactamase (37%), followed by type A (33%). We found 29 allotypes and 43 different substitutions in BlaZ. A single allotype, designated BlaZ-2, showed a robust and statistically significant association with the CzIE. Two other allotypes (BlaZ-3 and BlaZ-5) were associated with a lack of the CzIE. Three amino acid substitutions (A9V, E112A, and G145E) showed statistically significant association with the CzIE (P β <0.01). CC30 was the predominant clone among isolates displaying the CzIE. Thus, we provide a novel approach to the classification of the staphylococcal β-lactamases with the potential to more accurately identify MSSA strains exhibiting the CzIE. | en_US |
dc.language.iso | eng | |
dc.publisher | American Society for Microbiology | |
dc.relation.ispartofseries | Antimicrobial Agents and Chemotherapy | |
dc.rights | info:eu-repo/semantics/restrictedAccess | |
dc.rights.uri | https://creativecommons.org/licenses/by-nc-nd/4.0/deed.es | |
dc.subject | BlaZ allotypes | en_US |
dc.subject | cefazolin | en_US |
dc.subject | inoculum effect | en_US |
dc.subject | MSSA | en_US |
dc.title | Novel insights into the classification of staphylococcal β-lactamases in relation to the cefazolin inoculum effect | en_US |
dc.type | info:eu-repo/semantics/article | |
dc.identifier.doi | https://doi.org/10.1128/AAC.02511-19 | |
dc.subject.ocde | https://purl.org/pe-repo/ocde/ford#3.03.08 | |
dc.subject.ocde | https://purl.org/pe-repo/ocde/ford#3.01.05 | |
dc.relation.issn | 1098-6596 |
Ficheros | Tamaño | Formato | Ver |
---|---|---|---|
No hay ficheros asociados a este ítem. |