Complementation of the Mycoplasma synoviae MS-H vaccine strain with wild-type oppF influences its growth
Somayeh Kordafshari1, Marc S Marenda1, Rebecca Agnew1
1Asia Pacific Centre for Animal Health, Melbourne Veterinary School, Faculty of Veterinary & Agricultural Sciences, The University of Melbourne, Werribee, Australia.
Abstract:
The Mycoplasma synoviae (MS) vaccine strain MS-H harbours a frameshift mutation in oppF (oligopeptide permease transporter) which results in expression of a truncated OppF1. The effect of this mutation on growth and attenuation of the MS-H is unknown. In this study, the impact of the mutation on the vaccine phenotype was investigated in vitro by introducing a wild-type copy of oppF gene in the MS-H genome. Wild-type oppF was cloned under the vlhA promoter into an oriC vector carrying a tetracycline resistance gene. MS-H was successfully transformed with the final construct pMS-oppF1-tetM or with a similar vector lacking oppF coding sequence (pMS-tetM). The MS-H transformed with pMS-oppF1-tetM exhibited smaller colony size than MS-H transformed with pMS-tetM. Monospecific rabbit sera against C-terminus of OppF1 detected bands of expected size for full-length OppF1 in the 86079/7NS parental strain of MS-H and the MS-H transformed with pMS-oppF1-tetM, but not in MS-H and MS-H transformed with pMS-tetM. Comparison of the growth curve of MS-H transformants harvested from media with/without tetracycline was conducted using vlhA Q-PCR which revealed that MS-H transformed with pMS-tetM had a higher growth rate than MS-H transformed with pMS-oppF1-tetM in the media with/without tetracycline. Lastly, the whole genome sequencing of MS-H transformed with pMS-oppF1-tetM (passage 27) showed that the chromosomal copy of the mutated oppF had been replaced with a wild-type version of the gene. This study reveals that the truncation of oppF impacts on growth characteristics of the MS-H and provides insight into the molecular pathogenesis of MS and perhaps broader mycoplasma species.RESEARCH HIGHLIGHTS The full-length OppF1 was expressed in Mycoplasma synoviae MS-H vaccine.Truncation of oppF impacts on growth characteristics of the MS-H.Chromosomal copy of the mutated oppF in MS-H was replaced with wild-type oppF.
Insights
The Mycoplasma synoviae (MS) vaccine strain MS-H
Area of Science:
- Veterinary Microbiology
- Molecular Biology
- Vaccine Development
Background:
- The Mycoplasma synoviae (MS) vaccine strain MS-H has a mutation in the oligopeptide permease transporter (oppF) gene, leading to a truncated OppF1 protein.
- The impact of this OppF1 truncation on MS-H growth and attenuation remains unclear.
Purpose of the Study:
- To investigate the effect of OppF1 truncation on the MS-H vaccine phenotype by reintroducing a wild-type oppF gene.
- To understand the role of OppF1 in Mycoplasma synoviae growth and pathogenesis.
Main Methods:
- Introducing a wild-type oppF gene into the MS-H genome using a vector under the vlhA promoter.
- Transforming MS-H with constructs containing either wild-type oppF or a control vector.
- Analyzing colony size, OppF1 protein expression via Western blot, and growth rates using qPCR.
- Confirming gene replacement through whole-genome sequencing.
Main Results:
- MS-H transformed with wild-type oppF showed smaller colony size compared to controls.
- Full-length OppF1 protein was detected in MS-H with reintroduced wild-type oppF, but not in control MS-H.
- MS-H with the control vector exhibited a higher growth rate than MS-H with wild-type oppF.
- Whole-genome sequencing confirmed the replacement of the mutated oppF with the wild-type gene.
Conclusions:
- OppF1 truncation significantly impacts the growth characteristics of the Mycoplasma synoviae MS-H vaccine strain.
- This study provides insights into the molecular mechanisms underlying MS pathogenesis and potential implications for other Mycoplasma species.
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