Filamentous-haemagglutinin-like protein genes encoded on a plasmid of Moraxella bovis
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Updated: Aug 6, 2026

Enrichment of Native and Recombinant Extracellular Vesicles of Mycobacteria
Published on: December 8, 2023
Tsutomu Kakuda1, Nopporn Sarataphan, Tetsuya Tanaka
1Department of Animal Hygiene, School of Veterinary Medicine and Animal Sciences, Kitasato University, Higashi 23, 35-1, Towada, Aomori 034-8628, Japan. kakuda@vmas.kitasato-u.ac.jp
Abstract:
The complete nucleotide sequence of a plasmid, pMBO-1, from Moraxella bovis strain Epp63 was determined. We identified 30 open reading frames (ORFs) encoded by the 44,215bp molecule. Two large ORFs, flpA and flpB, encoding proteins with similarity to Bordetella pertussis filamentous haemagglutinin (FHA), were identified on the same plasmid. The gene for a specific accessory protein (Fap), which may play a role in the secretion of Flp protein, was also identified. Reverse transcriptase PCR analysis of total RNA isolated from M. bovis Epp63 indicated that the flpA, flpB, and fap genes are all transcribed. Southern blot analysis indicated that the flp and fap genes are present in other clinical isolates of geographically diverse M. bovis.
Insights
The Moraxella bovis plasmid pMBO-1 contains genes (flpA, flpB, fap) similar to Bordetella pertussis FHA, which are transcribed and present in diverse clinical isolates.
Area of Science:
- Microbiology
- Molecular Biology
- Genomics
Background:
- Moraxella bovis is an important pathogen in cattle.
- Plasmids play a significant role in bacterial adaptation and virulence.
- Understanding plasmid-borne genes in M. bovis can reveal mechanisms of pathogenesis.
Purpose of the Study:
- To determine the complete nucleotide sequence of the plasmid pMBO-1 from Moraxella bovis strain Epp63.
- To identify and characterize genes with potential roles in M. bovis virulence and adaptation.
- To investigate the presence and transcription of identified genes in clinical isolates.
Main Methods:
- Plasmid DNA isolation and sequencing.
- Open reading frame (ORF) identification and analysis.
- Reverse transcriptase PCR (RT-PCR) for gene transcription analysis.
- Southern blot hybridization for gene distribution analysis.
Main Results:
- The 44,215bp plasmid pMBO-1 was fully sequenced, revealing 30 ORFs.
- Two large ORFs, flpA and flpB, encoding proteins homologous to Bordetella pertussis filamentous hemagglutinin (FHA), were identified.
- A gene for an accessory protein (Fap), potentially involved in Flp secretion, was also found.
- RT-PCR confirmed the transcription of flpA, flpB, and fap genes.
- Southern blot analysis showed that flp and fap genes are present in geographically diverse M. bovis clinical isolates.
Conclusions:
- The pMBO-1 plasmid harbors genes (flpA, flpB, fap) with potential implications for Moraxella bovis pathogenesis.
- These genes are actively transcribed and conserved across different M. bovis clinical strains, suggesting functional importance.
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