Please use this identifier to cite or link to this item: https://doi.org/10.1007/s00018-018-2827-7
DC FieldValue
dc.titleEngineering microbes for targeted strikes against human pathogens
dc.contributor.authorHwang, In Young
dc.contributor.authorLee, Hui Ling
dc.contributor.authorHuang, James Guoxian
dc.contributor.authorLim, Yvonne Yijuan
dc.contributor.authorYew, Wen Shan
dc.contributor.authorLee, Yung Seng
dc.contributor.authorChang, Matthew Wook
dc.date.accessioned2022-02-25T01:41:27Z
dc.date.available2022-02-25T01:41:27Z
dc.date.issued2018-08-01
dc.identifier.citationHwang, In Young, Lee, Hui Ling, Huang, James Guoxian, Lim, Yvonne Yijuan, Yew, Wen Shan, Lee, Yung Seng, Chang, Matthew Wook (2018-08-01). Engineering microbes for targeted strikes against human pathogens. CELLULAR AND MOLECULAR LIFE SCIENCES 75 (15) : 2719-2733. ScholarBank@NUS Repository. https://doi.org/10.1007/s00018-018-2827-7
dc.identifier.issn1420682X
dc.identifier.issn14209071
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/216136
dc.description.abstractLack of pathogen specificity in antimicrobial therapy causes non-discriminant microbial cell killing that disrupts the microflora present. As a result, potentially helpful microbial cells are killed along with the pathogen, altering the biodiversity and dynamic interactions within the population. Moreover, the unwarranted exposure of antibiotics to microbes increases the likelihood of developing resistance and perpetuates the emergence of multidrug resistance. Synthetic biology offers an alternative solution where specificity can be conferred to reduce the non-specific, non-targeted activity of currently available antibiotics, and instead provides targeted therapy against specific pathogens and minimising collateral damage to the host’s inherent microbiota. With a greater understanding of the microbiome and the available genetic engineering tools for microbial cells, it is possible to devise antimicrobial strategies for novel antimicrobial therapy that are able to precisely and selectively remove infectious pathogens. Herein, we review the strategies developed by unlocking some of the natural mechanisms used by the microbes and how these may be utilised in targeted antimicrobial therapy, with the promise of reducing the current global bane of multidrug antimicrobial resistance.
dc.language.isoen
dc.publisherSPRINGER BASEL AG
dc.sourceElements
dc.subjectScience & Technology
dc.subjectLife Sciences & Biomedicine
dc.subjectBiochemistry & Molecular Biology
dc.subjectCell Biology
dc.subjectTargeted therapy
dc.subjectSynthetic biology
dc.subjectInfectious pathogen
dc.subjectLive biotherapeutics
dc.subjectMicrobiome
dc.subjectPhage engineering
dc.subjectAntimicrobial peptide
dc.subjectAntibiotic resistance
dc.subjectS-TYPE PYOCIN
dc.subjectESCHERICHIA-COLI
dc.subjectSTAPHYLOCOCCUS-AUREUS
dc.subjectBACTERIOPHAGE THERAPY
dc.subjectNEXT-GENERATION
dc.subjectPHAGE THERAPY
dc.subjectINFECTION
dc.subjectRESISTANCE
dc.subjectPROBIOTICS
dc.subjectCOCKTAIL
dc.typeReview
dc.date.updated2022-02-24T05:07:50Z
dc.contributor.departmentBIOCHEMISTRY
dc.contributor.departmentPAEDIATRICS
dc.description.doi10.1007/s00018-018-2827-7
dc.description.sourcetitleCELLULAR AND MOLECULAR LIFE SCIENCES
dc.description.volume75
dc.description.issue15
dc.description.page2719-2733
dc.published.statePublished
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