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Published on: January 7, 2019
Characterization of Pasteurella multocida type B capsule biosynthesis proteins
Thomas R Smallman1, Chantelle M Cairns2, Frank St Michael2
1Infection Program, Monash Biomedicine Discovery Institute, Department of Microbiology, Monash University, Victoria, Australia.
Researchers identified key proteins (BcbC, BcbE, BcbG, BcbH) essential for Pasteurella multocida type B capsule biosynthesis. These findings advance understanding of this animal pathogen
Area of Science:
- Bacteriology
- Molecular Biology
- Animal Health
Background:
- Pasteurella multocida causes severe animal diseases like hemorrhagic septicemia.
- Type B capsule is crucial for hemorrhagic septicemia, composed of N-acetyl glucosamine (GlcNAc) and N-acetyl mannosaminuronic acid (ManNAcA) with fructose and glycine side chains.
Purpose of the Study:
- To investigate the proteins involved in type B capsule biosynthesis in P. multocida strain M1404.
- To elucidate the roles of specific genes (bcbC, bcbE, bcbG, bcbH) in capsule production and structure.
Main Methods:
- Capsule absorbance assays, Alcian blue stains, and Western blots were used to assess capsule production and export.
- In-source collision-induced dissociation mass spectrometry determined capsule structure.
- Gene inactivation and heterologous expression were employed to study gene function.
Main Results:
- BcbC was identified as the likely capsule synthase.
- BcbE and BcbG are involved in fructose side chain addition, and BcbH is the probable glycine transferase.
- Inactivation of bcbE, bcbG, or bcbH significantly reduced capsule production. Heterologous expression of bcbABCDI produced the type B main chain in a capsule mutant.
Conclusions:
- The identified bcb genes are necessary and sufficient for the synthesis of the type B P. multocida capsule main chain.
- Understanding these genes provides insights into Pasteurella multocida pathogenesis and potential targets for control.
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