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Metabolism of Toxic Sugars by Strains of the Bee Gut Symbiont Gilliamella apicola
Social bees collect carbohydrate-rich food to support their colonies, and yet, certain carbohydrates present in their diet or produced through the breakdown of pollen are toxic to bees. The gut microbiota of social bees is dominated by a few core bacterial species, including the Gram-negative specie...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5090037/ https://www.ncbi.nlm.nih.gov/pubmed/27803186 http://dx.doi.org/10.1128/mBio.01326-16 |
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author | Zheng, Hao Nishida, Alex Kwong, Waldan K. Koch, Hauke Engel, Philipp Steele, Margaret I. Moran, Nancy A. |
author_facet | Zheng, Hao Nishida, Alex Kwong, Waldan K. Koch, Hauke Engel, Philipp Steele, Margaret I. Moran, Nancy A. |
author_sort | Zheng, Hao |
collection | PubMed |
description | Social bees collect carbohydrate-rich food to support their colonies, and yet, certain carbohydrates present in their diet or produced through the breakdown of pollen are toxic to bees. The gut microbiota of social bees is dominated by a few core bacterial species, including the Gram-negative species Gilliamella apicola. We isolated 42 strains of G. apicola from guts of honey bees and bumble bees and sequenced their genomes. All of the G. apicola strains share high 16S rRNA gene similarity, but they vary extensively in gene repertoires related to carbohydrate metabolism. Predicted abilities to utilize different sugars were verified experimentally. Some strains can utilize mannose, arabinose, xylose, or rhamnose (monosaccharides that can cause toxicity in bees) as their sole carbon and energy source. All of the G. apicola strains possess a manO-associated mannose family phosphotransferase system; phylogenetic analyses suggest that this was acquired from Firmicutes through horizontal gene transfer. The metabolism of mannose is specifically dependent on the presence of mannose-6-phosphate isomerase (MPI). Neither growth rates nor the utilization of glucose and fructose are affected in the presence of mannose when the gene encoding MPI is absent from the genome, suggesting that mannose is not taken up by G. apicola strains which harbor the phosphotransferase system but do not encode the MPI. Given their ability to simultaneously utilize glucose, fructose, and mannose, as well as the ability of many strains to break down other potentially toxic carbohydrates, G. apicola bacteria may have key roles in improving dietary tolerances and maintaining the health of their bee hosts. |
format | Online Article Text |
id | pubmed-5090037 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-50900372016-11-11 Metabolism of Toxic Sugars by Strains of the Bee Gut Symbiont Gilliamella apicola Zheng, Hao Nishida, Alex Kwong, Waldan K. Koch, Hauke Engel, Philipp Steele, Margaret I. Moran, Nancy A. mBio Research Article Social bees collect carbohydrate-rich food to support their colonies, and yet, certain carbohydrates present in their diet or produced through the breakdown of pollen are toxic to bees. The gut microbiota of social bees is dominated by a few core bacterial species, including the Gram-negative species Gilliamella apicola. We isolated 42 strains of G. apicola from guts of honey bees and bumble bees and sequenced their genomes. All of the G. apicola strains share high 16S rRNA gene similarity, but they vary extensively in gene repertoires related to carbohydrate metabolism. Predicted abilities to utilize different sugars were verified experimentally. Some strains can utilize mannose, arabinose, xylose, or rhamnose (monosaccharides that can cause toxicity in bees) as their sole carbon and energy source. All of the G. apicola strains possess a manO-associated mannose family phosphotransferase system; phylogenetic analyses suggest that this was acquired from Firmicutes through horizontal gene transfer. The metabolism of mannose is specifically dependent on the presence of mannose-6-phosphate isomerase (MPI). Neither growth rates nor the utilization of glucose and fructose are affected in the presence of mannose when the gene encoding MPI is absent from the genome, suggesting that mannose is not taken up by G. apicola strains which harbor the phosphotransferase system but do not encode the MPI. Given their ability to simultaneously utilize glucose, fructose, and mannose, as well as the ability of many strains to break down other potentially toxic carbohydrates, G. apicola bacteria may have key roles in improving dietary tolerances and maintaining the health of their bee hosts. American Society for Microbiology 2016-11-01 /pmc/articles/PMC5090037/ /pubmed/27803186 http://dx.doi.org/10.1128/mBio.01326-16 Text en Copyright © 2016 Zheng et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (http://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Article Zheng, Hao Nishida, Alex Kwong, Waldan K. Koch, Hauke Engel, Philipp Steele, Margaret I. Moran, Nancy A. Metabolism of Toxic Sugars by Strains of the Bee Gut Symbiont Gilliamella apicola |
title | Metabolism of Toxic Sugars by Strains of the Bee Gut Symbiont Gilliamella apicola |
title_full | Metabolism of Toxic Sugars by Strains of the Bee Gut Symbiont Gilliamella apicola |
title_fullStr | Metabolism of Toxic Sugars by Strains of the Bee Gut Symbiont Gilliamella apicola |
title_full_unstemmed | Metabolism of Toxic Sugars by Strains of the Bee Gut Symbiont Gilliamella apicola |
title_short | Metabolism of Toxic Sugars by Strains of the Bee Gut Symbiont Gilliamella apicola |
title_sort | metabolism of toxic sugars by strains of the bee gut symbiont gilliamella apicola |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5090037/ https://www.ncbi.nlm.nih.gov/pubmed/27803186 http://dx.doi.org/10.1128/mBio.01326-16 |
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