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Potential and use of bacterial small RNAs to combat drug resistance: a systematic review

BACKGROUND: Over the decades, new antibacterial agents have been developed in an attempt to combat drug resistance, but they remain unsuccessful. Recently, a novel class of bacterial gene expression regulators, bacterial small RNAs (sRNAs), has received increasing attention toward their involvement...

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Autores principales: Chan, Hung, Ho, Jeffery, Liu, Xiaodong, Zhang, Lin, Wong, Sunny Hei, Chan, Matthew TV, Wu, William KK
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5736357/
https://www.ncbi.nlm.nih.gov/pubmed/29290689
http://dx.doi.org/10.2147/IDR.S148444
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author Chan, Hung
Ho, Jeffery
Liu, Xiaodong
Zhang, Lin
Wong, Sunny Hei
Chan, Matthew TV
Wu, William KK
author_facet Chan, Hung
Ho, Jeffery
Liu, Xiaodong
Zhang, Lin
Wong, Sunny Hei
Chan, Matthew TV
Wu, William KK
author_sort Chan, Hung
collection PubMed
description BACKGROUND: Over the decades, new antibacterial agents have been developed in an attempt to combat drug resistance, but they remain unsuccessful. Recently, a novel class of bacterial gene expression regulators, bacterial small RNAs (sRNAs), has received increasing attention toward their involvement in antibiotic resistance. This systematic review aimed to discuss the potential of these small molecules as antibacterial drug targets. METHODS: Two investigators performed a comprehensive search of MEDLINE, EmBase, and ISI Web of Knowledge from inception to October 2016, without restriction on language. We included all in vitro and in vivo studies investigating the role of bacterial sRNA in antibiotic resistance. Risk of bias of the included studies was assessed by a modified guideline of Systematic Review Center for Laboratory Animal Experimentation (SYRCLE). RESULTS: Initial search yielded 432 articles. After exclusion of non-original articles, 20 were included in this review. Of these, all studies examined bacterial-type strains only. There were neither relevant in vivo nor clinical studies. The SYRCLE scores ranged from to 5 to 7, with an average of 5.9. This implies a moderate risk of bias. sRNAs influenced the antibiotics susceptibility through modulation of gene expression relevant to efflux pumps, cell wall synthesis, and membrane proteins. CONCLUSION: Preclinical studies on bacterial-type strains suggest that modulation of sRNAs could enhance bacterial susceptibility to antibiotics. Further studies on clinical isolates and in vivo models are needed to elucidate the therapeutic value of sRNA modulation on treatment of multidrug-resistant bacterial infection.
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spelling pubmed-57363572017-12-29 Potential and use of bacterial small RNAs to combat drug resistance: a systematic review Chan, Hung Ho, Jeffery Liu, Xiaodong Zhang, Lin Wong, Sunny Hei Chan, Matthew TV Wu, William KK Infect Drug Resist Review BACKGROUND: Over the decades, new antibacterial agents have been developed in an attempt to combat drug resistance, but they remain unsuccessful. Recently, a novel class of bacterial gene expression regulators, bacterial small RNAs (sRNAs), has received increasing attention toward their involvement in antibiotic resistance. This systematic review aimed to discuss the potential of these small molecules as antibacterial drug targets. METHODS: Two investigators performed a comprehensive search of MEDLINE, EmBase, and ISI Web of Knowledge from inception to October 2016, without restriction on language. We included all in vitro and in vivo studies investigating the role of bacterial sRNA in antibiotic resistance. Risk of bias of the included studies was assessed by a modified guideline of Systematic Review Center for Laboratory Animal Experimentation (SYRCLE). RESULTS: Initial search yielded 432 articles. After exclusion of non-original articles, 20 were included in this review. Of these, all studies examined bacterial-type strains only. There were neither relevant in vivo nor clinical studies. The SYRCLE scores ranged from to 5 to 7, with an average of 5.9. This implies a moderate risk of bias. sRNAs influenced the antibiotics susceptibility through modulation of gene expression relevant to efflux pumps, cell wall synthesis, and membrane proteins. CONCLUSION: Preclinical studies on bacterial-type strains suggest that modulation of sRNAs could enhance bacterial susceptibility to antibiotics. Further studies on clinical isolates and in vivo models are needed to elucidate the therapeutic value of sRNA modulation on treatment of multidrug-resistant bacterial infection. Dove Medical Press 2017-12-15 /pmc/articles/PMC5736357/ /pubmed/29290689 http://dx.doi.org/10.2147/IDR.S148444 Text en © 2017 Chan et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Review
Chan, Hung
Ho, Jeffery
Liu, Xiaodong
Zhang, Lin
Wong, Sunny Hei
Chan, Matthew TV
Wu, William KK
Potential and use of bacterial small RNAs to combat drug resistance: a systematic review
title Potential and use of bacterial small RNAs to combat drug resistance: a systematic review
title_full Potential and use of bacterial small RNAs to combat drug resistance: a systematic review
title_fullStr Potential and use of bacterial small RNAs to combat drug resistance: a systematic review
title_full_unstemmed Potential and use of bacterial small RNAs to combat drug resistance: a systematic review
title_short Potential and use of bacterial small RNAs to combat drug resistance: a systematic review
title_sort potential and use of bacterial small rnas to combat drug resistance: a systematic review
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5736357/
https://www.ncbi.nlm.nih.gov/pubmed/29290689
http://dx.doi.org/10.2147/IDR.S148444
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