Discovery of the novel auxiliary factor for β-lactam resistance BlrA in community-acquired methicillin-resistant Staphylococcus aureus

Methicillin-resistant Staphylococcus aureus (MRSA) is one of the most important human pathogens that cause a variety of infections in community and hospital settings. This organism displays high levels of resistance to β-lactam antibiotics and this principally occurs due to the production of β-lacta...

Полное описание

Сохранить в:
Библиографические подробности
Главный автор: Astudillo Skliarova, Igor Eduardo (author)
Формат: article
Язык:spa
Опубликовано: 2023
Online-ссылка:http://revistas.espoch.edu.ec/index.php/cssn/article/view/790
Метки: Добавить метку
Нет меток, Требуется 1-ая метка записи!
_version_ 1859125646853144576
author Astudillo Skliarova, Igor Eduardo
author_facet Astudillo Skliarova, Igor Eduardo
author_role author
collection Revista CSSN
dc.creator.none.fl_str_mv Astudillo Skliarova, Igor Eduardo
dc.date.none.fl_str_mv 2023-04-26
dc.format.none.fl_str_mv application/pdf
text/html
dc.identifier.none.fl_str_mv http://revistas.espoch.edu.ec/index.php/cssn/article/view/790
dc.language.none.fl_str_mv spa
dc.publisher.none.fl_str_mv Escuela Superior Politécnica de Chimborazo
dc.relation.none.fl_str_mv http://revistas.espoch.edu.ec/index.php/cssn/article/view/790/783
http://revistas.espoch.edu.ec/index.php/cssn/article/view/790/803
dc.rights.none.fl_str_mv Derechos de autor 2023 Igor Eduardo Astudillo Skliarova
http://creativecommons.org/licenses/by-nc/4.0
info:eu-repo/semantics/openAccess
dc.source.none.fl_str_mv La Ciencia al Servicio de la Salud y la Nutrición; Vol. 14 Núm. 1 (2023): Enero 2023 - Junio 2023; SECCIÓN_B_49-56
La Ciencia al Servicio de la Salud y la Nutrición; Vol. 14 Núm. 1 (2023): Enero 2023 - Junio 2023; SECCIÓN_B_49-56
1390-874X
reponame:Revista CSSN
instname:Escuela Superior Politécnica de Chimborazo
instacron:ESPOCH
dc.title.none.fl_str_mv
Discovery of the novel auxiliary factor for β-lactam resistance BlrA in community-acquired methicillin-resistant Staphylococcus aureus
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
description Methicillin-resistant Staphylococcus aureus (MRSA) is one of the most important human pathogens that cause a variety of infections in community and hospital settings. This organism displays high levels of resistance to β-lactam antibiotics and this principally occurs due to the production of β-lactamase and the penicillin binding protein PBP2a encoded by mecA gene. Furthermore, additional mechanisms, such as auxiliary factors, significantly contribute to β-lactam resistance. However, the function of most of these factors is still unknown. Recently, in our laboratory, the novel auxiliary factor gene blrA was initially identified by transposon mutagenesis in the community-acquired MRSA strain JE2. Next, the transposon mutation was transduced to the community-acquired MRSA strain MW2, resulting in the formation of a transposon mutant for blrA (blrA::ermB), denoted as MW2A. Initially, our results suggested that MW2A is more susceptible to oxacillin than the MW2 wild-type. Then, we performed the Minimum Inhibitory Concentration (MIC) method for the β-lactam antibiotics: oxacillin, cefoxitin, cephradine, ceftazidime, cefaclor and imipenem. MW2A exhibited a two-fold reduction for all tested β-lactam antibiotics compared to the MRSA wild-type strain MW2. Additionally, no phenotypical changes were observed after performing PBP2a latex agglutination test and phage spot assay. Finally, using DeepTMHMM we show that BlrA is likely to act intracellularly, which is typical of auxiliary factors. In this study, we show that BlrA is clearly involved in β-lactam resistance, but does not affect the expression of the gene mecA or the structure of the wall teichoic acids. Furthermore, we propose that that BlrA acts as an auxiliary factor and is activated in response to antimicrobial stress.
eu_rights_str_mv openAccess
format article
id REVCSSN_06590a6290ba477476aa545fed3e4765
instacron_str ESPOCH
institution ESPOCH
instname_str Escuela Superior Politécnica de Chimborazo
language spa
network_acronym_str REVCSSN
network_name_str Revista CSSN
oai_identifier_str oai:ojs.172.17.102.145:article/790
publishDate 2023
publisher.none.fl_str_mv Escuela Superior Politécnica de Chimborazo
reponame_str Revista CSSN
repository.mail.fl_str_mv
repository.name.fl_str_mv Revista CSSN - Escuela Superior Politécnica de Chimborazo
repository_id_str 0
rights_invalid_str_mv Derechos de autor 2023 Igor Eduardo Astudillo Skliarova
http://creativecommons.org/licenses/by-nc/4.0
spelling Discovery of the novel auxiliary factor for β-lactam resistance BlrA in community-acquired methicillin-resistant Staphylococcus aureusAstudillo Skliarova, Igor EduardoMethicillin-resistant Staphylococcus aureus (MRSA) is one of the most important human pathogens that cause a variety of infections in community and hospital settings. This organism displays high levels of resistance to β-lactam antibiotics and this principally occurs due to the production of β-lactamase and the penicillin binding protein PBP2a encoded by mecA gene. Furthermore, additional mechanisms, such as auxiliary factors, significantly contribute to β-lactam resistance. However, the function of most of these factors is still unknown. Recently, in our laboratory, the novel auxiliary factor gene blrA was initially identified by transposon mutagenesis in the community-acquired MRSA strain JE2. Next, the transposon mutation was transduced to the community-acquired MRSA strain MW2, resulting in the formation of a transposon mutant for blrA (blrA::ermB), denoted as MW2A. Initially, our results suggested that MW2A is more susceptible to oxacillin than the MW2 wild-type. Then, we performed the Minimum Inhibitory Concentration (MIC) method for the β-lactam antibiotics: oxacillin, cefoxitin, cephradine, ceftazidime, cefaclor and imipenem. MW2A exhibited a two-fold reduction for all tested β-lactam antibiotics compared to the MRSA wild-type strain MW2. Additionally, no phenotypical changes were observed after performing PBP2a latex agglutination test and phage spot assay. Finally, using DeepTMHMM we show that BlrA is likely to act intracellularly, which is typical of auxiliary factors. In this study, we show that BlrA is clearly involved in β-lactam resistance, but does not affect the expression of the gene mecA or the structure of the wall teichoic acids. Furthermore, we propose that that BlrA acts as an auxiliary factor and is activated in response to antimicrobial stress.Methicillin-resistant Staphylococcus aureus (MRSA) is one of the most important human pathogens that cause a variety of infections in community and hospital settings. This organism displays high levels of resistance to β-lactam antibiotics and this principally occurs due to the production of β-lactamase and the penicillin binding protein PBP2a encoded by mecA gene. Furthermore, additional mechanisms, such as auxiliary factors, significantly contribute to β-lactam resistance. However, the function of most of these factors is still unknown. Recently, in our laboratory, the novel auxiliary factor gene blrA was initially identified by transposon mutagenesis in the community-acquired MRSA strain JE2. Next, the transposon mutation was transduced to the community-acquired MRSA strain MW2, resulting in the formation of a transposon mutant for blrA (blrA::ermB), denoted as MW2A. Initially, our results suggested that MW2A is more susceptible to oxacillin than the MW2 wild-type. Then, we performed the Minimum Inhibitory Concentration (MIC) method for the β-lactam antibiotics: oxacillin, cefoxitin, cephradine, ceftazidime, cefaclor and imipenem. MW2A exhibited a two-fold reduction for all tested β-lactam antibiotics compared to the MRSA wild-type strain MW2. Additionally, no phenotypical changes were observed after performing PBP2a latex agglutination test and phage spot assay. Finally, using DeepTMHMM we show that BlrA is likely to act intracellularly, which is typical of auxiliary factors. In this study, we show that BlrA is clearly involved in β-lactam resistance, but does not affect the expression of the gene mecA or the structure of the wall teichoic acids. Furthermore, we propose that that BlrA acts as an auxiliary factor and is activated in response to antimicrobial stress.Escuela Superior Politécnica de Chimborazo2023-04-26info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdftext/htmlhttp://revistas.espoch.edu.ec/index.php/cssn/article/view/790La Ciencia al Servicio de la Salud y la Nutrición; Vol. 14 Núm. 1 (2023): Enero 2023 - Junio 2023; SECCIÓN_B_49-56La Ciencia al Servicio de la Salud y la Nutrición; Vol. 14 Núm. 1 (2023): Enero 2023 - Junio 2023; SECCIÓN_B_49-561390-874Xreponame:Revista CSSNinstname:Escuela Superior Politécnica de Chimborazoinstacron:ESPOCHspahttp://revistas.espoch.edu.ec/index.php/cssn/article/view/790/783http://revistas.espoch.edu.ec/index.php/cssn/article/view/790/803Derechos de autor 2023 Igor Eduardo Astudillo Skliarovahttp://creativecommons.org/licenses/by-nc/4.0info:eu-repo/semantics/openAccess2023-05-31T21:09:20Zoai:ojs.172.17.102.145:article/790Portal de revistashttp://revistas.espoch.edu.ec/index.php/cssn/Universidad públicahttps://espoch.edu.ecEcuador1390-874X1390-874Xopendoar:02025-10-05T18:04:08.025535Revista CSSN - Escuela Superior Politécnica de Chimborazotrue
spellingShingle Discovery of the novel auxiliary factor for β-lactam resistance BlrA in community-acquired methicillin-resistant Staphylococcus aureus
Astudillo Skliarova, Igor Eduardo
status_str publishedVersion
title Discovery of the novel auxiliary factor for β-lactam resistance BlrA in community-acquired methicillin-resistant Staphylococcus aureus
title_full Discovery of the novel auxiliary factor for β-lactam resistance BlrA in community-acquired methicillin-resistant Staphylococcus aureus
title_fullStr Discovery of the novel auxiliary factor for β-lactam resistance BlrA in community-acquired methicillin-resistant Staphylococcus aureus
title_full_unstemmed Discovery of the novel auxiliary factor for β-lactam resistance BlrA in community-acquired methicillin-resistant Staphylococcus aureus
title_short Discovery of the novel auxiliary factor for β-lactam resistance BlrA in community-acquired methicillin-resistant Staphylococcus aureus
title_sort Discovery of the novel auxiliary factor for β-lactam resistance BlrA in community-acquired methicillin-resistant Staphylococcus aureus
url http://revistas.espoch.edu.ec/index.php/cssn/article/view/790