YwdL in Bacillus cereus: Its Role in Germination and Exosporium Structure

• Published in: PloS one Vol. 6; no. 8; p. e23801
• Main Authors: Terry, Cassandra, Shepherd, Andrew, Radford, David S., Moir, Anne, Bullough, Per A.
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 24.08.2011; Public Library of Science (PLoS)
• Subjects: Antibodies; Bacillus anthracis; Bacillus cereus; Bacillus cereus - chemistry; Bacillus cereus - ultrastructure; Bacillus subtilis; Bacillus thuringiensis; Bacterial Proteins - physiology; Bacterial Proteins - ultrastructure; Biology; Biotechnology; Cell Wall; Crystallography; Enzymes; Freeze-thawing; Germination; Labeling; Labelling; Localization; Medicine; Microscopy; Microscopy, Electron, Transmission; Molecular biology; Phenotypes; Plant Epidermis; Proteins; Spore coats; Spores; Spores, Bacterial - chemistry; Spores, Bacterial - ultrastructure; Thawing; Western blotting; United Kingdom > UK
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0023801

In members of the Bacillus cereus group the outermost layer of the spore is the exosporium, which interacts with hosts and the environment. Efforts have been made to identify proteins of the exosporium but only a few have so far been characterised and their role in determining spore architecture and spore function is still poorly understood. We have characterised the exosporium protein, YwdL. ΔywdL spores have a more fragile exosporium, subject to damage on repeated freeze-thawing, although there is no evidence of altered resistance properties, and coats appear intact. Immunogold labelling and Western blotting with anti-YwdL antibodies identified YwdL to be located exclusively on the inner surface of the exosporium of B. cereus and B. thuringiensis. We conclude that YwdL is important for formation of a robust exosporium but is not required to maintain the crystalline assembly within the basal layer or for attachment of the hairy nap structure. ΔywdL spores are unable to germinate in response to CaDPA, and have altered germination properties, a phenotype that confirms the expected defect in localization of the cortex lytic enzyme CwlJ in the coat.