An Interplay of Multiple Positive and Negative Factors Governs Methicillin Resistance in Staphylococcus aureus
The development of resistance to β-lactam antibiotics has made Staphylococcus aureus a clinical burden on a global scale. MRSA (methicillin-resistant S. aureus) is commonly known as a superbug. The ability of MRSA to proliferate in the presence of β-lactams is attributed to the acquisition of , whic...
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Veröffentlicht in: | Microbiology and molecular biology reviews 2022-06, Vol.86 (2), p.e0015921 |
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creator | Bilyk, Bohdan L Panchal, Viralkumar V Tinajero-Trejo, Mariana Hobbs, Jamie K Foster, Simon J |
description | The development of resistance to β-lactam antibiotics has made Staphylococcus aureus a clinical burden on a global scale. MRSA (methicillin-resistant S. aureus) is commonly known as a superbug. The ability of MRSA to proliferate in the presence of β-lactams is attributed to the acquisition of
, which encodes the alternative penicillin binding protein, PBP2A, which is insensitive to the antibiotics. Most MRSA isolates exhibit low-level β-lactam resistance, whereby additional genetic adjustments are required to develop high-level resistance. Although several genetic factors that potentiate or are required for high-level resistance have been identified, how these interact at the mechanistic level has remained elusive. Here, we discuss the development of resistance and assess the role of the associated components in tailoring physiology to accommodate incoming
. |
doi_str_mv | 10.1128/mmbr.00159-21 |
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, which encodes the alternative penicillin binding protein, PBP2A, which is insensitive to the antibiotics. Most MRSA isolates exhibit low-level β-lactam resistance, whereby additional genetic adjustments are required to develop high-level resistance. Although several genetic factors that potentiate or are required for high-level resistance have been identified, how these interact at the mechanistic level has remained elusive. Here, we discuss the development of resistance and assess the role of the associated components in tailoring physiology to accommodate incoming
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, which encodes the alternative penicillin binding protein, PBP2A, which is insensitive to the antibiotics. Most MRSA isolates exhibit low-level β-lactam resistance, whereby additional genetic adjustments are required to develop high-level resistance. Although several genetic factors that potentiate or are required for high-level resistance have been identified, how these interact at the mechanistic level has remained elusive. Here, we discuss the development of resistance and assess the role of the associated components in tailoring physiology to accommodate incoming
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Panchal, Viralkumar V ; Tinajero-Trejo, Mariana ; Hobbs, Jamie K ; Foster, Simon J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a450t-6823b737f8050f99f5f9678246cf0a26c74f3426cdcb3b5f460b763794e4ae4f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Amides</topic><topic>Anti-Bacterial Agents - therapeutic use</topic><topic>Antibiotic resistance</topic><topic>Antibiotics</topic><topic>Antimicrobial Chemotherapy</topic><topic>Bacterial Proteins - genetics</topic><topic>Bacterial Proteins - metabolism</topic><topic>Drug resistance</topic><topic>Genetic factors</topic><topic>Humans</topic><topic>Methicillin</topic><topic>Methicillin Resistance - genetics</topic><topic>Methicillin-Resistant Staphylococcus aureus - genetics</topic><topic>Penicillin</topic><topic>Penicillin-Binding Proteins - genetics</topic><topic>Penicillin-Binding Proteins - metabolism</topic><topic>Resistance factors</topic><topic>Review</topic><topic>Staphylococcal Infections - drug therapy</topic><topic>Staphylococcus aureus</topic><topic>Staphylococcus aureus - genetics</topic><topic>β-Lactam antibiotics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bilyk, Bohdan L</creatorcontrib><creatorcontrib>Panchal, Viralkumar V</creatorcontrib><creatorcontrib>Tinajero-Trejo, Mariana</creatorcontrib><creatorcontrib>Hobbs, Jamie K</creatorcontrib><creatorcontrib>Foster, Simon J</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Microbiology and molecular biology reviews</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bilyk, Bohdan L</au><au>Panchal, Viralkumar V</au><au>Tinajero-Trejo, Mariana</au><au>Hobbs, Jamie K</au><au>Foster, Simon J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>An Interplay of Multiple Positive and Negative Factors Governs Methicillin Resistance in Staphylococcus aureus</atitle><jtitle>Microbiology and molecular biology reviews</jtitle><stitle>Microbiol Mol Biol Rev</stitle><addtitle>Microbiol Mol Biol Rev</addtitle><date>2022-06-15</date><risdate>2022</risdate><volume>86</volume><issue>2</issue><spage>e0015921</spage><pages>e0015921-</pages><issn>1092-2172</issn><eissn>1098-5557</eissn><abstract>The development of resistance to β-lactam antibiotics has made Staphylococcus aureus a clinical burden on a global scale. MRSA (methicillin-resistant S. aureus) is commonly known as a superbug. The ability of MRSA to proliferate in the presence of β-lactams is attributed to the acquisition of
, which encodes the alternative penicillin binding protein, PBP2A, which is insensitive to the antibiotics. Most MRSA isolates exhibit low-level β-lactam resistance, whereby additional genetic adjustments are required to develop high-level resistance. Although several genetic factors that potentiate or are required for high-level resistance have been identified, how these interact at the mechanistic level has remained elusive. Here, we discuss the development of resistance and assess the role of the associated components in tailoring physiology to accommodate incoming
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subjects | Amides Anti-Bacterial Agents - therapeutic use Antibiotic resistance Antibiotics Antimicrobial Chemotherapy Bacterial Proteins - genetics Bacterial Proteins - metabolism Drug resistance Genetic factors Humans Methicillin Methicillin Resistance - genetics Methicillin-Resistant Staphylococcus aureus - genetics Penicillin Penicillin-Binding Proteins - genetics Penicillin-Binding Proteins - metabolism Resistance factors Review Staphylococcal Infections - drug therapy Staphylococcus aureus Staphylococcus aureus - genetics β-Lactam antibiotics |
title | An Interplay of Multiple Positive and Negative Factors Governs Methicillin Resistance in Staphylococcus aureus |
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