Assembly of Complete Genome Sequences of Negative-Control and Experimental Strain Variants of Staphylococcus aureus ATCC BAA-39 Selected under the Effect of the Drug FS-1, Which Induces Antibiotic Resistance Reversion
- PMID: 31346020
- PMCID: PMC6658690
- DOI: 10.1128/MRA.00579-19
Assembly of Complete Genome Sequences of Negative-Control and Experimental Strain Variants of Staphylococcus aureus ATCC BAA-39 Selected under the Effect of the Drug FS-1, Which Induces Antibiotic Resistance Reversion
Abstract
Staphylococcus aureus ATCC BAA-39 is the reference organism for a multidrug-resistant Staphylococcus aureus (MRSA) strain that was used to study drug-induced resistance reversion by an iodine-containing nanomolecular complex, FS-1. PacBio sequencing was performed on both the experimental and control strains, followed by genome assembly, variant calling, and DNA modification profiling.
Copyright © 2019 Joubert et al.
References
-
- Ilin AI, Kulmanov ME, Korotetskiy IS, Islamov RA, Akhmetova GK, Lankina MV, Reva ON. 2017. Genomic insight into mechanisms of reversion of antibiotic resistance in multidrug resistant Mycobacterium tuberculosis induced by a nanomolecular iodine-containing complex FS-1. Front Cell Infect Microbiol 7:151. doi: 10.3389/fcimb.2017.00151. - DOI - PMC - PubMed
-
- Kalykova A, Kustova T, Sakipova Z, Ibragimova N, Islamov R, Vetchý D, Ilin A. 2016. Acute and subchronic toxicity studies of the original drug FS-1. Acta Vet Brno 85:9–16. doi: 10.2754/avb201685010009. - DOI
-
- Korotetskiy I, Shilov S, Shvidko S, Jumagaziyeva A, Suldina NA, Korotetskaya NV, Ilin A, Reva O. 2017. Transcriptional response of the multidrug resistant Staphylococcus aureus following FS-1 exposure. Eurasian J Appl Biotechnol 2017:43–48. doi: 10.11134/btp.3.2017.6. - DOI
-
- Garrigós C, Murillo O, Lora-Tamayo J, Verdaguer R, Tubau F, Cabellos C, Cabo J, Ariza J. 2012. Efficacy of daptomycin-cloxacillin combination in experimental foreign-body infection due to methicillin-resistant Staphylococcus aureus. Antimicrob Agents Chemother 56:3806–3811. doi: 10.1128/AAC.00127-12. - DOI - PMC - PubMed
LinkOut - more resources
Full Text Sources