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Culture-independent Discovery of the Malacidins As Calcium-dependent Antibiotics with Activity Against Multidrug-resistant Gram-positive Pathogens

Overview
Journal Nat Microbiol
Date 2018 Feb 14
PMID 29434326
Citations 155
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Abstract

Despite the wide availability of antibiotics, infectious diseases remain a leading cause of death worldwide . In the absence of new therapies, mortality rates due to untreatable infections are predicted to rise more than tenfold by 2050. Natural products (NPs) made by cultured bacteria have been a major source of clinically useful antibiotics. In spite of decades of productivity, the use of bacteria in the search for new antibiotics was largely abandoned due to high rediscovery rates. As only a fraction of bacterial diversity is regularly cultivated in the laboratory and just a fraction of the chemistries encoded by cultured bacteria are detected in fermentation experiments, most bacterial NPs remain hidden in the global microbiome. In an effort to access these hidden NPs, we have developed a culture-independent NP discovery platform that involves sequencing, bioinformatic analysis and heterologous expression of biosynthetic gene clusters captured on DNA extracted from environmental samples. Here, we describe the application of this platform to the discovery of the malacidins, a distinctive class of antibiotics that are commonly encoded in soil microbiomes but have never been reported in culture-based NP discovery efforts. The malacidins are active against multidrug-resistant pathogens, sterilize methicillin-resistant Staphylococcus aureus skin infections in an animal wound model and did not select for resistance under our laboratory conditions.

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References
1.
Kleijn L, Oppedijk S, t Hart P, van Harten R, Martin-Visscher L, Kemmink J . Total Synthesis of Laspartomycin C and Characterization of Its Antibacterial Mechanism of Action. J Med Chem. 2016; 59(7):3569-74. DOI: 10.1021/acs.jmedchem.6b00219. View

2.
Katz M, Hover B, Brady S . Culture-independent discovery of natural products from soil metagenomes. J Ind Microbiol Biotechnol. 2015; 43(2-3):129-41. DOI: 10.1007/s10295-015-1706-6. View

3.
Medema M, Blin K, Cimermancic P, de Jager V, Zakrzewski P, Fischbach M . antiSMASH: rapid identification, annotation and analysis of secondary metabolite biosynthesis gene clusters in bacterial and fungal genome sequences. Nucleic Acids Res. 2011; 39(Web Server issue):W339-46. PMC: 3125804. DOI: 10.1093/nar/gkr466. View

4.
Zhang T, Luo Y, Chen Y, Li X, Yu J . BIGrat: a repeat resolver for pyrosequencing-based re-sequencing with Newbler. BMC Res Notes. 2012; 5:567. PMC: 3599625. DOI: 10.1186/1756-0500-5-567. View

5.
Reddy B, Milshteyn A, Charlop-Powers Z, Brady S . eSNaPD: a versatile, web-based bioinformatics platform for surveying and mining natural product biosynthetic diversity from metagenomes. Chem Biol. 2014; 21(8):1023-33. PMC: 4157589. DOI: 10.1016/j.chembiol.2014.06.007. View