Melioidosis patient serum-reactive synthetic tetrasaccharides bearing the predominant epitopes of Burkholderia pseudomallei and Burkholderia mallei O-antigens. Issue 39 (12th September 2019)
- Record Type:
- Journal Article
- Title:
- Melioidosis patient serum-reactive synthetic tetrasaccharides bearing the predominant epitopes of Burkholderia pseudomallei and Burkholderia mallei O-antigens. Issue 39 (12th September 2019)
- Main Title:
- Melioidosis patient serum-reactive synthetic tetrasaccharides bearing the predominant epitopes of Burkholderia pseudomallei and Burkholderia mallei O-antigens
- Authors:
- Cloutier, Maude
Delar, Emmanilo
Muru, Kevin
Ndong, Seynabou
Hoyeck, Robert R.
Kaewarpai, Taniya
Chantratita, Narisara
Burtnick, Mary N.
Brett, Paul J.
Gauthier, Charles - Abstract:
- Abstract : Tetrasaccharides mimicking Burkholderia pseudomallei and Burkholderia mallei lipopolysaccharide O-antigens were synthesized and found to be highly reactive with Thai melioidosis patient serum, highlighting their potential as vaccine candidates. Abstract : Melioidosis and glanders, respectively caused by the Gram-negative bacteria Burkholderia pseudomallei ( Bp ) and Burkholderia mallei ( Bm ), are considered as urgent public health issues in developing countries and potential bioterrorism agents. Bp and Bm lipopolysaccharides (LPS) have been identified as attractive vaccine candidates for the development of prophylactic measures against melioidosis and glanders. Bp and Bm express structurally similar LPSs wherein the O-antigen (OAg) portion consists of a heteropolymer whose repeating unit is a disaccharide composed of d -glucose and 6-deoxy-l -talose residues, the latter being diversely acetylated and methylated. Herein we report the synthesis of two tetrasaccharides mimicking the main substitution epitopes of Bp and Bm LPS OAgs. The assembly of the tetrasaccharides was achieved using a sequential glycosylation strategy while relying on the late-stage epimerization of the inner rhamnose into a 6-deoxy-l -talose residue. We show that these synthetic compounds strongly react with culture-confirmed Thai melioidosis patient serum and closely mimic the antigenicity of native Bp OAg. Our results suggest that these tetrasaccharides could be suitable candidates for theAbstract : Tetrasaccharides mimicking Burkholderia pseudomallei and Burkholderia mallei lipopolysaccharide O-antigens were synthesized and found to be highly reactive with Thai melioidosis patient serum, highlighting their potential as vaccine candidates. Abstract : Melioidosis and glanders, respectively caused by the Gram-negative bacteria Burkholderia pseudomallei ( Bp ) and Burkholderia mallei ( Bm ), are considered as urgent public health issues in developing countries and potential bioterrorism agents. Bp and Bm lipopolysaccharides (LPS) have been identified as attractive vaccine candidates for the development of prophylactic measures against melioidosis and glanders. Bp and Bm express structurally similar LPSs wherein the O-antigen (OAg) portion consists of a heteropolymer whose repeating unit is a disaccharide composed of d -glucose and 6-deoxy-l -talose residues, the latter being diversely acetylated and methylated. Herein we report the synthesis of two tetrasaccharides mimicking the main substitution epitopes of Bp and Bm LPS OAgs. The assembly of the tetrasaccharides was achieved using a sequential glycosylation strategy while relying on the late-stage epimerization of the inner rhamnose into a 6-deoxy-l -talose residue. We show that these synthetic compounds strongly react with culture-confirmed Thai melioidosis patient serum and closely mimic the antigenicity of native Bp OAg. Our results suggest that these tetrasaccharides could be suitable candidates for the development of vaccines and/or diagnostic tools against melioidosis and glanders. … (more)
- Is Part Of:
- Organic & biomolecular chemistry. Volume 17:Issue 39(2019)
- Journal:
- Organic & biomolecular chemistry
- Issue:
- Volume 17:Issue 39(2019)
- Issue Display:
- Volume 17, Issue 39 (2019)
- Year:
- 2019
- Volume:
- 17
- Issue:
- 39
- Issue Sort Value:
- 2019-0017-0039-0000
- Page Start:
- 8878
- Page End:
- 8901
- Publication Date:
- 2019-09-12
- Subjects:
- Chemistry, Organic -- Periodicals
Bioorganic chemistry -- Periodicals
Chemistry, Physical organic -- Periodicals
547 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/ob#!recentarticles&all ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c9ob01711a ↗
- Languages:
- English
- ISSNs:
- 1477-0520
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6286.350000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 20401.xml