The Impairment of Methyl Metabolism From luxS Mutation of Streptococcus mutans

The luxS gene is present in a wide range of bacteria and is involved in many cellular processes. LuxS mutation can cause autoinducer(AI)-2 deficiency and methyl metabolism disorder. The objective of this study was to demonstrate that, in addition to AI-2-mediated quorum sensing (QS), methyl metaboli...

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Main Authors: Xuchen Hu, Yuxia Wang, Li Gao, Wenxin Jiang, Wenzhen Lin, Chenguang Niu, Keyong Yuan, Rui Ma, Zhengwei Huang
Format: Article
Language:English
Published: Frontiers Media S.A. 2018-03-01
Series:Frontiers in Microbiology
Subjects:
Online Access:http://journal.frontiersin.org/article/10.3389/fmicb.2018.00404/full
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author Xuchen Hu
Yuxia Wang
Li Gao
Wenxin Jiang
Wenzhen Lin
Chenguang Niu
Keyong Yuan
Rui Ma
Zhengwei Huang
author_facet Xuchen Hu
Yuxia Wang
Li Gao
Wenxin Jiang
Wenzhen Lin
Chenguang Niu
Keyong Yuan
Rui Ma
Zhengwei Huang
author_sort Xuchen Hu
collection DOAJ
description The luxS gene is present in a wide range of bacteria and is involved in many cellular processes. LuxS mutation can cause autoinducer(AI)-2 deficiency and methyl metabolism disorder. The objective of this study was to demonstrate that, in addition to AI-2-mediated quorum sensing (QS), methyl metabolism plays an important role in LuxS regulation in Streptococcus mutans. The sahH gene from Pseudomonas aeruginosa was amplified and introduced into the S. mutans luxS-null strain to complement the methyl metabolism disruption in a defective QS phenotype. The intracellular activated methyl cycle (AMC) metabolites [S-adenosylmethionine (SAM), S-adenosylhomocysteine (SAH), homocysteine (HCY), and methionine] were quantified in wild-type S. mutans and its three derivatives to determine the metabolic effects of disrupting the AMC. Biofilm mass and structure, acid tolerance, acid production, exopolysaccharide synthesis of multispecies biofilms and the transcriptional level of related genes were determined. The results indicated that SAH and SAM were relatively higher in S. mutans luxS-null strain and S. mutans luxS null strain with plasmid pIB169 when cultured overnight, and HCY was significantly higher in S. mutans UA159. Consistent with the transcriptional profile, luxS deletion-mediated impairment of biofilm formation and acid tolerance was restored to wild-type levels using transgenic SahH. These results also suggest that methionine methyl metabolism contributes to LuxS regulation in S. mutans to a significant degree.
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spelling doaj.art-b659f52ac75741b5885ae4a736a68eb62022-12-22T01:30:05ZengFrontiers Media S.A.Frontiers in Microbiology1664-302X2018-03-01910.3389/fmicb.2018.00404329699The Impairment of Methyl Metabolism From luxS Mutation of Streptococcus mutansXuchen Hu0Yuxia Wang1Li Gao2Wenxin Jiang3Wenzhen Lin4Chenguang Niu5Keyong Yuan6Rui Ma7Zhengwei Huang8Department of Endodontics, Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai Key Laboratory of Stomatology & Shanghai Research Institute of Stomatology, National Clinical Research Center of Stomatology, Shanghai, ChinaDepartment of Endodontics, Tianjin Stomatological Hospital, Nankai University, Tianjin, ChinaDepartment of Endodontics, Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai Key Laboratory of Stomatology & Shanghai Research Institute of Stomatology, National Clinical Research Center of Stomatology, Shanghai, ChinaDepartment of Endodontics, Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai Key Laboratory of Stomatology & Shanghai Research Institute of Stomatology, National Clinical Research Center of Stomatology, Shanghai, ChinaDepartment of Endodontics, Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai Key Laboratory of Stomatology & Shanghai Research Institute of Stomatology, National Clinical Research Center of Stomatology, Shanghai, ChinaDepartment of Endodontics, Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai Key Laboratory of Stomatology & Shanghai Research Institute of Stomatology, National Clinical Research Center of Stomatology, Shanghai, ChinaDepartment of Endodontics, Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai Key Laboratory of Stomatology & Shanghai Research Institute of Stomatology, National Clinical Research Center of Stomatology, Shanghai, ChinaDepartment of Endodontics, Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai Key Laboratory of Stomatology & Shanghai Research Institute of Stomatology, National Clinical Research Center of Stomatology, Shanghai, ChinaDepartment of Endodontics, Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai Key Laboratory of Stomatology & Shanghai Research Institute of Stomatology, National Clinical Research Center of Stomatology, Shanghai, ChinaThe luxS gene is present in a wide range of bacteria and is involved in many cellular processes. LuxS mutation can cause autoinducer(AI)-2 deficiency and methyl metabolism disorder. The objective of this study was to demonstrate that, in addition to AI-2-mediated quorum sensing (QS), methyl metabolism plays an important role in LuxS regulation in Streptococcus mutans. The sahH gene from Pseudomonas aeruginosa was amplified and introduced into the S. mutans luxS-null strain to complement the methyl metabolism disruption in a defective QS phenotype. The intracellular activated methyl cycle (AMC) metabolites [S-adenosylmethionine (SAM), S-adenosylhomocysteine (SAH), homocysteine (HCY), and methionine] were quantified in wild-type S. mutans and its three derivatives to determine the metabolic effects of disrupting the AMC. Biofilm mass and structure, acid tolerance, acid production, exopolysaccharide synthesis of multispecies biofilms and the transcriptional level of related genes were determined. The results indicated that SAH and SAM were relatively higher in S. mutans luxS-null strain and S. mutans luxS null strain with plasmid pIB169 when cultured overnight, and HCY was significantly higher in S. mutans UA159. Consistent with the transcriptional profile, luxS deletion-mediated impairment of biofilm formation and acid tolerance was restored to wild-type levels using transgenic SahH. These results also suggest that methionine methyl metabolism contributes to LuxS regulation in S. mutans to a significant degree.http://journal.frontiersin.org/article/10.3389/fmicb.2018.00404/fullStreptococcus mutansmethionine metabolismLuxSSahHhigh-performance liquid chromatography–tandem mass spectrometry
spellingShingle Xuchen Hu
Yuxia Wang
Li Gao
Wenxin Jiang
Wenzhen Lin
Chenguang Niu
Keyong Yuan
Rui Ma
Zhengwei Huang
The Impairment of Methyl Metabolism From luxS Mutation of Streptococcus mutans
Frontiers in Microbiology
Streptococcus mutans
methionine metabolism
LuxS
SahH
high-performance liquid chromatography–tandem mass spectrometry
title The Impairment of Methyl Metabolism From luxS Mutation of Streptococcus mutans
title_full The Impairment of Methyl Metabolism From luxS Mutation of Streptococcus mutans
title_fullStr The Impairment of Methyl Metabolism From luxS Mutation of Streptococcus mutans
title_full_unstemmed The Impairment of Methyl Metabolism From luxS Mutation of Streptococcus mutans
title_short The Impairment of Methyl Metabolism From luxS Mutation of Streptococcus mutans
title_sort impairment of methyl metabolism from luxs mutation of streptococcus mutans
topic Streptococcus mutans
methionine metabolism
LuxS
SahH
high-performance liquid chromatography–tandem mass spectrometry
url http://journal.frontiersin.org/article/10.3389/fmicb.2018.00404/full
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