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.

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.

Related Concept Videos

Development of Immunocompetence01:22

Development of Immunocompetence

The initiation of cell-mediated immunity can be observed as early as the third month of fetal growth, with active antibody-mediated immunity following approximately one month later.
The initial cells that migrate from the fetal thymus settle within the skin and epithelial tissues lining the mouth, digestive tract, and in females, the uterus and vagina. These cells, including skin-based dendritic cells, serve as antigen-presenting cells, playing a key role in T cell activation.
Subsequent T...
686
Mismatch Repair01:20

Mismatch Repair

Organisms are capable of detecting and fixing nucleotide mismatches that occur during DNA replication. This sophisticated process requires identifying the new strand and replacing the erroneous bases with correct nucleotides. Mismatch repair is coordinated by many proteins in both prokaryotes and eukaryotes.
The Mutator Protein Family Plays a Key Role in DNA Mismatch Repair
The human genome has more than 3 billion base pairs of DNA per cell. Prior to cell division, that vast amount of genetic...
6.2K
Microbial Growth Media01:27

Microbial Growth Media

Microbial growth media are essential tools in microbiology, providing the nutrients and conditions necessary to cultivate and study microorganisms. These media are categorized by their composition, consistency, and functional roles, enabling researchers to investigate microbial physiology, behavior, and interactions.Types and Consistencies of Growth MediaGrowth media can be solid, liquid, or semisolid. Solid media, often agar-based, allow visible colony growth for isolation and enumeration.
1.1K