<HashMap><database>biostudies-literature</database><scores><citationCount>0</citationCount><reanalysisCount>0</reanalysisCount><viewCount>47</viewCount><searchCount>0</searchCount></scores><additional><omics_type>Unknown</omics_type><volume>6(5)</volume><submitter>Fisher JF</submitter><pubmed_abstract>The value of the β-lactam antibiotics for the control of bacterial infection has eroded with time. Three Gram-positive human pathogens that were once routinely susceptible to β-lactam chemotherapy-Streptococcus pneumoniae, Enterococcus faecium, and Staphylococcus aureus-now are not. Although a fourth bacterium, the acid-fast (but not Gram-positive-staining) Mycobacterium tuberculosis, has intrinsic resistance to earlier β-lactams, the emergence of strains of this bacterium resistant to virtually all other antibiotics has compelled the evaluation of newer β-lactam combinations as possible contributors to the multidrug chemotherapy required to control tubercular infection. The emerging molecular-level understanding of these resistance mechanisms used by these four bacteria provides the conceptual framework for bringing forward new β-lactams, and new β-lactam strategies, for the future control of their infections.</pubmed_abstract><journal>Cold Spring Harbor perspectives in medicine</journal><pagination>a025221</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4852796</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>β-Lactam Resistance Mechanisms: Gram-Positive Bacteria and Mycobacterium tuberculosis.</pubmed_title><pmcid>PMC4852796</pmcid><pubmed_authors>Mobashery S</pubmed_authors><pubmed_authors>Fisher JF</pubmed_authors><view_count>47</view_count></additional><is_claimable>false</is_claimable><name>β-Lactam Resistance Mechanisms: Gram-Positive Bacteria and Mycobacterium tuberculosis.</name><description>The value of the β-lactam antibiotics for the control of bacterial infection has eroded with time. Three Gram-positive human pathogens that were once routinely susceptible to β-lactam chemotherapy-Streptococcus pneumoniae, Enterococcus faecium, and Staphylococcus aureus-now are not. Although a fourth bacterium, the acid-fast (but not Gram-positive-staining) Mycobacterium tuberculosis, has intrinsic resistance to earlier β-lactams, the emergence of strains of this bacterium resistant to virtually all other antibiotics has compelled the evaluation of newer β-lactam combinations as possible contributors to the multidrug chemotherapy required to control tubercular infection. The emerging molecular-level understanding of these resistance mechanisms used by these four bacteria provides the conceptual framework for bringing forward new β-lactams, and new β-lactam strategies, for the future control of their infections.</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 May</publication><modification>2024-11-08T18:29:12.944Z</modification><creation>2019-06-06T15:45:59Z</creation></dates><accession>S-EPMC4852796</accession><cross_references><pubmed>27091943</pubmed><doi>10.1101/cshperspect.a025221</doi></cross_references></HashMap>