Peptidoglycan synthesis in Tannerella forsythia: Scavenging is the modus operandi

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Abstract
Summary: Tannerella forsythia is a Gram‐negative oral pathogen strongly associated with periodontitis. This bacterium has an absolute requirement for exogenous N‐acetylmuramic acid (MurNAc), an amino sugar that forms the repeating disaccharide unit with amino sugar N‐acetylglucosamine (GlcNAc) of the peptidoglycan backbone. In silico genome analysis indicates that T. forsythia lacks the key biosynthetic enzymes needed for the de novo synthesis of MurNAc, and so relies on alternative ways to meet its requirement for peptidoglycan biosynthesis. In the subgingival niche, the bacterium can acquire MurNAc and peptidoglycan fragments (muropeptides) released by the cohabiting bacteria during their cell wall breakdown associated with cell division. Tannerella forsythia is able to also use host sialic acid (Neu5Ac) in lieu of MurNAc or muropeptides for its survival during the biofilm growth. Evidence suggests that the bacterium might be able to shunt sialic acid into a metabolic pathway leading to peptidoglycan synthesis. In this review, we explore the mechanisms by which T. forsythia is able to scavenge MurNAc, muropeptide and sialic acid for its peptidoglycan synthesis, and the impact of these scavenging activities on pathogenesis.
Funding Information
  • National Institute of Dental and Craniofacial Research (DE023526)
  • National Institute of Dental and Craniofacial Research (DE14749, DE22870)

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