The Genome Structure of Ciprofloxacin-Resistant Mycoplasma Hominis Clinical Isolates.

Acta Naturae

Academician I.N. Blokhina Nizhny Novgorod Scientific Research Institute of Epidemiology and Microbiology, Federal Service for Surveillance on Customers Rights Protection and Human Wellbeing, Nizhniy Novgorod, 603950 Russia.

Published: January 2020

The genome structure of three ciprofloxacin-resistant clinical isolates was studied using next-generation sequencing on the Illumina platform. The protein sequences of the studied strains were found to have a high degree of homology. (M45, M57, MH1866) was shown to have limited biosynthetic capabilities, associated with the predominance of the genes encoding the proteins involved in catabolic processes. Multiple single-nucleotide substitutions causing intraspecific polymorphism of were found. The genes encoding the efflux systems - ABC transporters (the ATP-binding cassette superfamily) and proteins of the MATE (multidrug and toxic compound extrusion) family - were identified. The molecular mechanism of ciprofloxacin resistance of the M45 and M57 isolates was found to be associated with the Ser83Leu substitution in DNA gyrase subunit A. In the MH1866 isolate it was related to the Lys144Arg substitution in topoisomerase IV subunit A.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7245959PMC
http://dx.doi.org/10.32607/actanaturae.10941DOI Listing

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