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In vitro activity of bioactive extracts from rare actinomycetes against multi‐drug resistant Streptococcus pneumoniae
Author(s) -
Tiwari K.,
Raj V.S.,
Upadhyay D.J.,
Gupta R.K.
Publication year - 2015
Publication title -
journal of applied microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.889
H-Index - 156
eISSN - 1365-2672
pISSN - 1364-5072
DOI - 10.1111/jam.12810
Subject(s) - streptococcus pneumoniae , microbiology and biotechnology , in vitro , minimum inhibitory concentration , antimicrobial , biology , levofloxacin , antibiotics , biochemistry
Aims In this study, we investigated the in vitro potential of the bioactive extracts from five putatively novel species of actinomycetes isolated from the Indian hot desert against multi‐drug resistant (MDR) S treptococcus pneumoniae . Methods and Results The antimicrobial activity of 10 different extracts was evaluated against S. pneumoniae strains with, erm ( B ) and mef ( E ) genes as well as fluoroquinolone‐resistant ( FQ R ) strains using the micro‐broth dilution method. Of these 10 extracts, four exhibited good to excellent anti‐ S. pneumoniae activity with minimum inhibitory concentrations ( MIC s) ranging from 0·125 to 8 μ g ml −1 . The time‐kill kinetics study showed that these extracts killed the pathogens in 2–8 h. In vitro cell‐free transcription/translation of luciferase gene using S30 bacterial extract and TNT mammalian ribosome indicated that they inhibited bacterial ribosomes at much lower concentrations than those required to inhibit the mammalian ribosomes. Conclusions This study demonstrates that these are potent concentration‐dependent bactericidal metabolites with 16‐fold higher in vitro activity than levofloxacin against MDR S. pneumoniae . Significance and Impact of the Study Metabolites from actinomycetes can be excellent inhibitors of MDR S. pneumoniae . Considering the in vitro efficacy of these crude extracts against S. pneumoniae MDR spp., once purified these can be used against streptococcal pathogens causing community‐acquired pneumonia.