Galactofuranose in Mycoplasma mycoides is important for membrane integrity and conceals adhesins but does not contribute to serum resistance. Issue 1 (14th October 2015)
- Record Type:
- Journal Article
- Title:
- Galactofuranose in Mycoplasma mycoides is important for membrane integrity and conceals adhesins but does not contribute to serum resistance. Issue 1 (14th October 2015)
- Main Title:
- Galactofuranose in Mycoplasma mycoides is important for membrane integrity and conceals adhesins but does not contribute to serum resistance
- Authors:
- Schieck, Elise
Lartigue, Carole
Frey, Joachim
Vozza, Nicolas
Hegermann, Jan
Miller, Rachel A.
Valguarnera, Ezequiel
Muriuki, Cecilia
Meens, Jochen
Nene, Vish
Naessens, Jan
Weber, Johann
Lowary, Todd L.
Vashee, Sanjay
Feldman, Mario F.
Jores, Joerg - Abstract:
- Summary: M ycoplasma mycoides subsp. capri ( M mc ) and subsp. mycoides ( M mm ) are important ruminant pathogens worldwide causing diseases such as pleuropneumonia, mastitis and septicaemia. They express galactofuranose residues on their surface, but their role in pathogenesis has not yet been determined. The M . mycoides genomes contain up to several copies of the glf gene, which encodes an enzyme catalysing the last step in the synthesis of galactofuranose. We generated a deletion of the glf gene in a strain of M mc using genome transplantation and tandem repeat endonuclease coupled cleavage (TREC) with yeast as an intermediary host for the genome editing. As expected, the resulting YCp1.1‐Δ glf strain did not produce the galactofuranose‐containing glycans as shown by immunoblots and immuno‐electronmicroscopy employing a galactofuranose specific monoclonal antibody. The mutant lacking galactofuranose exhibited a decreased growth rate and a significantly enhanced adhesion to small ruminant cells. The mutant was also 'leaking' as revealed by a β‐galactosidase‐based assay employing a membrane impermeable substrate. These findings indicate that galactofuranose‐containing polysaccharides conceal adhesins and are important for membrane integrity. Unexpectedly, the mutant strain showed increased serum resistance. Abstract : To provide insights into the functional role of UDP‐galactopyranose mutase and capsular galactan in Mycoplasma mycoides, we made use of synthetic genomicSummary: M ycoplasma mycoides subsp. capri ( M mc ) and subsp. mycoides ( M mm ) are important ruminant pathogens worldwide causing diseases such as pleuropneumonia, mastitis and septicaemia. They express galactofuranose residues on their surface, but their role in pathogenesis has not yet been determined. The M . mycoides genomes contain up to several copies of the glf gene, which encodes an enzyme catalysing the last step in the synthesis of galactofuranose. We generated a deletion of the glf gene in a strain of M mc using genome transplantation and tandem repeat endonuclease coupled cleavage (TREC) with yeast as an intermediary host for the genome editing. As expected, the resulting YCp1.1‐Δ glf strain did not produce the galactofuranose‐containing glycans as shown by immunoblots and immuno‐electronmicroscopy employing a galactofuranose specific monoclonal antibody. The mutant lacking galactofuranose exhibited a decreased growth rate and a significantly enhanced adhesion to small ruminant cells. The mutant was also 'leaking' as revealed by a β‐galactosidase‐based assay employing a membrane impermeable substrate. These findings indicate that galactofuranose‐containing polysaccharides conceal adhesins and are important for membrane integrity. Unexpectedly, the mutant strain showed increased serum resistance. Abstract : To provide insights into the functional role of UDP‐galactopyranose mutase and capsular galactan in Mycoplasma mycoides, we made use of synthetic genomic tools such as genome transplantation and genome editing in yeast to create mutant strain YCpMmyc1.1‐Δ glf . Compared to its parental strain, YCpMmyc1.1‐Δ glf lacked galactofuranose‐containing galactan, showed a leaky membrane, had a reduced growth rate, exhibited increased adhesion to ruminant cells and showed increased serum resistance. … (more)
- Is Part Of:
- Molecular microbiology. Volume 99:Issue 1(2016)
- Journal:
- Molecular microbiology
- Issue:
- Volume 99:Issue 1(2016)
- Issue Display:
- Volume 99, Issue 1 (2016)
- Year:
- 2016
- Volume:
- 99
- Issue:
- 1
- Issue Sort Value:
- 2016-0099-0001-0000
- Page Start:
- 55
- Page End:
- 70
- Publication Date:
- 2015-10-14
- Subjects:
- Molecular microbiology -- Periodicals
572.829 - Journal URLs:
- http://www.blackwell-synergy.com/servlet/useragent?func=showIssues&code=mmi&close=2003#C2003 ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1365-2958 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/mmi.13213 ↗
- Languages:
- English
- ISSNs:
- 0950-382X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5900.817960
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 9881.xml