A GC-rich prophage-like genomic region of mycoplasma bovirhinis HAZ141_2 carries a gene cluster encoding resistance to kanamycin and neomycin

Inna Lysnyansky, Ilya Borovok*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

6 Scopus citations

Abstract

Recently, a complete genome sequence of Mycoplasma bovirhinis HAZ141_2 was published showing the presence of a 54-kB prophage-like region. Bioinformatic analysis revealed that this region has a more than 40% GC content and a chimeric organization with three structural elements-a prophage continuous region, a restriction-modification cassette, and a highly transmittable aadE-sat4-aphA-3 gene cluster found in both Gram-positive and Gram-negative bacteria. It is known that aadE confers resistance to streptomycin, sat4 governs resistance to streptothricin/nourseothricin, and aphA-3 is responsible for resistance to kanamycin and structurally related antibiotics. An aadE-like (aadE*) gene of strain HAZ141_2 encodes a 228-amino acid (aa) polypeptide whose carboxy-terminal domain (positions 44 to 206) is almost identical to that of a functional 302-aa AadE (positions 140 to 302). Transcription analysis of the aadE*-sat4-aphA-3 genes showed their cotranscription in M. bovirhinis HAZ141_2. Moreover, a common promoter for aadE*-sat4-aphA-3 was mapped upstream of aadE* using 59 rapid amplification of cDNA ends analysis. Determination of MICs to aminoglycosides and nourseothricin revealed that M. bovirhinis HAZ141_2 is highly resistant to kanamycin and neomycin ($512mg/ml). However, MICs to streptomycin (64mg/ml) and nourseothricin (16 to 32mg/ml) were similar to those identified in the prophageless M. bovirhinis type strain PG43 and Israeli field isolate 316981. We cloned the aadE*-sat4-aphA-3 genes into a low-copy-number vector and transferred them into antibiotic-sensitive Escherichia coli cells. While the obtained E. coli transformants were highly resistant to kanamycin, neomycin, and nourseothricin (MICs, $256mg/ml), there were no changes in MICs to streptomycin, suggesting a functional defect of the aadE*.

Original languageEnglish
Article numbere01010-20
JournalAntimicrobial Agents and Chemotherapy
Volume65
Issue number2
DOIs
StatePublished - Feb 2021

Funding

FundersFunder number
Istituto Zooprofilattico Sperimentale delle Venezie
National Institute of Animal Health
Salvatore Catania
National Agriculture and Food Research Organization
Veterinärmedizinische Universität Wien

    Keywords

    • AadE-sat4-aphA-3 gene cluster
    • Aminoglycosides
    • Horizontal gene transfer
    • Kanamycin and neomycin resistance
    • Mycoplasma bovirhinis
    • Prophage

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