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Probiotic supplements alleviate gestational diabetes mellitus by restoring the diversity of gut microbiota: a study based on 16S rRNA sequencing
Qing-Xiang Zheng , Xiu-Min Jiang , Hai-Wei Wang , Li Ge , Yu-Ting Lai , Xin-Yong Jiang , Fan Chen , Ping-Ping Huang
J. Microbiol. 2021;59(9):827-839.   Published online August 12, 2021
DOI: https://doi.org/10.1007/s12275-021-1094-8
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AbstractAbstract
Probiotics effectively prevent and improve metabolic diseases such as diabetes by regulating the intestinal microenvironment and gut microbiota. However, the effects of probiotics in gestational diabetes mellitus are not clear. Here, we showed that probiotic supplements significantly improved fasting blood glucose in a gestational diabetes mellitus rat model. To further understand the mechanisms of probiotics in gestational diabetes mellitus, the gut microbiota were analyzed via 16S rRNA sequencing. We found that compared with the normal pregnant group, the gestational diabetes mellitus rats had decreased diversity of gut microbiota. Moreover, probiotic supplementation restored the diversity of the gut microbiota in gestational diabetes mellitus rats, and the gut microbiota structure tended to be similar to that of normal pregnant rats. In particular, compared with gestational diabetes mellitus rats, the abundance of Firmicutes and Actinobacteria was higher after probiotic supplementation. Furthermore, activating carbohydrate metabolism and membrane transport pathways may be involved in the potential mechanisms by which probiotic supplements alleviate gestational diabetes mellitus. Overall, our results suggested that probiotic supplementation might be a novel approach to restore the gut microbiota of gestational diabetes mellitus rats and provided an experimental evidence for the use of probiotic supplements to treat gestational diabetes melitus.

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Citations to this article as recorded by  
  • Dietary Polyphenols Support Akkermansia muciniphila Growth via Mediation of the Gastrointestinal Redox Environment
    Charlene B. Van Buiten, Valerie A. Seitz, Jessica L. Metcalf, Ilya Raskin
    Antioxidants.2024; 13(3): 304.     CrossRef
  • The Intervention of Probiotics on Type 2 Diabetes Mellitus in Animal Models
    Qianyu Qu, Penggang He, Yuqi Zhang, Shujuan Yang, Peibin Zeng
    Molecular Nutrition & Food Research.2024;[Epub]     CrossRef
  • Lactobacillus gasseri BNR17 and Limosilactobacillus fermentum ABF21069 Ameliorate High Sucrose-Induced Obesity and Fatty Liver via Exopolysaccharide Production and β-oxidation
    Yu Mi Jo, Yoon Ji Son, Seul-Ah Kim, Gyu Min Lee, Chang Won Ahn, Han-Oh Park, Ji-Hyun Yun
    Journal of Microbiology.2024; 62(10): 907.     CrossRef
  • Probiotic therapy as a promising strategy for gestational diabetes mellitus management
    Deborah Emanuelle de Albuquerque Lemos, José Luiz de Brito Alves, Evandro Leite de Souza
    Expert Opinion on Biological Therapy.2024; 24(11): 1207.     CrossRef
  • Influence of Symbiotic Fermentation Broth on Regulating Metabolism with Gut Microbiota and Metabolite Profiles Is Estimated Using a Third-Generation Sequencing Platform
    Chih-Yin Wu, Chun-Kai Huang, Wei-Sheng Hong, Yin-Hsiu Liu, Ming-Chi Shih, Jung-Chun Lin
    Metabolites.2023; 13(9): 999.     CrossRef
  • Neuroprotective Effect of Ponicidin Alleviating the Diabetic Cognitive Impairment: Regulation of Gut Microbiota
    Xiaojuan Zhang, Feng Guo, Dujuan Cao, Yinan Yan, Ning Zhang, Kaili Zhang, Xinyi Li, Prashant Kumar, Xiaojuan Zhang
    Applied Biochemistry and Biotechnology.2023; 195(2): 735.     CrossRef
  • Antidiabetogenic mechanisms of probiotic action in food matrices: A review
    Vanessa Moraes Ramalho Castro, Rosa Helena Luchese
    PharmaNutrition.2022; 21: 100302.     CrossRef
  • Prepregnancy body mass index and gestational weight gain are associated with maternal and infant adverse outcomes in Chinese women with gestational diabetes
    Qing-Xiang Zheng, Hai-Wei Wang, Xiu-Min Jiang, Yan Lin, Gui-Hua Liu, Mian Pan, Li Ge, Xiao-Qian Chen, Jing-Ling Wu, Xiao-Yun Zhang, Yu-Qing Pan, Hong-Gu He
    Scientific Reports.2022;[Epub]     CrossRef
  • Probiotic Intervention in the Treatment of Diabetes Mellitus: A Review
    Navya Sreepathi, M.K. Jayanthi, S. Jagadeep Chandra, Shrisha Naik Bajpe, Ramith Ramu
    Journal of Pure and Applied Microbiology.2022; 16(3): 1519.     CrossRef
  • Ameliorative Effects of Bifidobacterium animalis subsp. lactis J-12 on Hyperglycemia in Pregnancy and Pregnancy Outcomes in a High-Fat-Diet/Streptozotocin-Induced Rat Model
    Jianjun Yang, Yumeng Ma, Tong Li, Yuanxiang Pang, Hongxing Zhang, Yuanhong Xie, Hui Liu, Yanfang Sun, Jianhua Ren, Junhua Jin
    Nutrients.2022; 15(1): 170.     CrossRef
  • Probiotic Mechanisms Affecting Glucose Homeostasis: A Scoping Review
    Maša Pintarič, Tomaž Langerholc
    Life.2022; 12(8): 1187.     CrossRef
  • The Roles of Probiotics in the Gut Microbiota Composition and Metabolic Outcomes in Asymptomatic Post-Gestational Diabetes Women: A Randomized Controlled Trial
    Zubaidah Hasain, Raja Affendi Raja Ali, Hajar Fauzan Ahmad, Ummul Fahri Abdul Rauf, Seok Fang Oon, Norfilza Mohd Mokhtar
    Nutrients.2022; 14(18): 3878.     CrossRef
  • Changes in the Gut Metabolic Profile of Gestational Diabetes Mellitus Rats Following Probiotic Supplementation
    Qing-Xiang Zheng, Hai-Wei Wang, Xiu-Min Jiang, Li Ge, Yu-Ting Lai, Xin-Yong Jiang, Ping-Ping Huang, Fan Chen, Xiao-Qian Chen
    Frontiers in Microbiology.2022;[Epub]     CrossRef
  • Microorganisms in the reproductive system and probiotic's regulatory effects on reproductive health
    Tao Feng, Yan Liu
    Computational and Structural Biotechnology Journal.2022; 20: 1541.     CrossRef
  • Several Shaping Characteristics of OneCurve Continuously Rotating System versus Three Different Kinematic Systems: ProTaper Universal, Twisted File Adaptive and WaveOne Gold
    Ali Türkyılmaz, Volkan Arıkan
    Meandros Medical and Dental Journal.2022; 23(1): 67.     CrossRef
Genetic diversity and population structure of the amylolytic yeast Saccharomycopsis fibuligera associated with Baijiu fermentation in China
Ju-Wei Wang , Pei-Jie Han , Da-Yong Han , Sen Zhou , Kuan Li , Peng-Yu He , Pan Zhen , Hui-Xin Yu , Zhen-Rong Liang , Xue-Wei Wang , Feng-Yan Bai
J. Microbiol. 2021;59(8):753-762.   Published online July 5, 2021
DOI: https://doi.org/10.1007/s12275-021-1115-7
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AbstractAbstract
The amylolytic yeast Saccharomycopsis fibuligera is a predominant species in starters and the early fermentation stage of Chinese liquor (Baijiu). However, the genetic diversity of the species remains largely unknown. Here we sequenced the genomes of 97 S. fibuligera strains from different Chinese Baijiu companies. The genetic diversity and population structure of the strains were analyzed based on 1,133 orthologous genes and the whole genome single nucleotide polymorphisms (SNPs). Four main lineages were recognized. One lineage contains 60 Chinese strains which are exclusively homozygous with relatively small genome sizes (18.55–18.72 Mb) and low sequence diversity. The strains clustered in the other three lineages are heterozygous with larger genomes (21.85–23.72 Mb) and higher sequence diversity. The genomes of the homozygous strains showed nearly 100% coverage with the genome of the reference strain KPH12 and the sub-genome A of the hybrid strain KJJ81 at the above 98% sequence identity level. The genomes of the heterozygous strains showed nearly 80% coverage with both the sub-genome A and the whole genome of KJJ81, suggesting that the Chinese heterozygous strains are also hybrids with nearly 20% genomes from an unidentified source. Eighty-three genes were found to show significant copy number variation between different lineages. However, remarkable lineage specific variations in glucoamylase and α-amylase activities and growth profiles in different carbon sources and under different environmental conditions were not observed, though strains exhibiting relatively high glucoamylase activity were mainly found from the homozygous lineage.

Citations

Citations to this article as recorded by  
  • Isolation of Saccharomycopsis species from plant material
    Carmen Dost, Florian Michling, Davies Kaimenyi, Mareike Rij, Jürgen Wendland
    Microbiological Research.2024; 283: 127691.     CrossRef
  • Microbial enzymes: the bridge between Daqu flavor and microbial communities
    Zelong Zhong, Tianyi Liu, Kaiping He, Min Zhong, Xiaoxue Chen, Yansong Xue, Beizhong Han, Diqiang Wang, Jun Liu
    Food Innovation and Advances.2024; 3(4): 426.     CrossRef
  • Exploring the heterogeneity of community and function and correspondence of “species-enzymes” among three types of Daqu with different fermentation peak-temperature via high-throughput sequencing and metagenomics
    Ying Huang, Dong Li, Yu Mu, Zhiyu Zhu, Yuzhang Wu, Qi Qi, Yingchun Mu, Wei Su
    Food Research International.2024; 176: 113805.     CrossRef
  • Deciphering the core microbes and their interactions in spontaneous Baijiu fermentation: A comprehensive review
    Jiamu Kang, Xiaoning Huang, Rengshu Li, Yuandi Zhang, Xiao-Xue Chen, Bei-Zhong Han
    Food Research International.2024; 188: 114497.     CrossRef
  • Correlational analysis of physicochemical indexes, microbial communities, and volatile components in light-flavor Daqu from north and south regions of China
    Qi Yu, Feiyan Mou, Junwen Xiao, Cheng Zhan, Liang Li, Xu Chang, Xiaoyuan Dong, Maobin Chen, Xinrui Wang, Mei Chen, Shangling Fang
    World Journal of Microbiology and Biotechnology.2024;[Epub]     CrossRef
  • Dynamic changes in volatile profiles and bacterial communities during natural fermentation of Mei yu, traditional Chinese fermented fish pieces
    Hongmei Yin, Qiang Hong, Xiang Yu, Hui Wang, Xiaodan Shi, Wei Liu, Tao Yuan, Zongcai Tu
    Food Research International.2024; 194: 114882.     CrossRef
  • Exploring the relationship between GuaYi levels and microbial-metabolic dynamics in Daqu
    Boyang Xu, Shanshan Xu, Hao Zhou, Ruijuan Wang, Chao Jiang, Dongdong Mu, Xuefeng Wu, Xiaolei Wu, Shaotong Jiang, Xingjiang Li
    Food Bioscience.2024; 60: 104347.     CrossRef
  • Exploring the Role of Active Functional Microbiota in Flavor Generation by Integrated Metatranscriptomics and Metabolomics during Niulanshan Baijiu Fermentation
    Yuanyuan Pan, Ying Wang, Wenjun Hao, Sen Zhou, Chengbao Duan, Qiushi Li, Jinwang Wei, Gang Liu
    Foods.2023; 12(22): 4140.     CrossRef
  • Dynamic changes and correlations of microbial communities, physicochemical properties, and volatile metabolites during Daqu fermentation of Taorong-type Baijiu
    Yanbo Liu, Haideng Li, Shumei Dong, Zhou Zhou, Zhenke Zhang, Runna Huang, Suna Han, Jianguang Hou, Chunmei Pan
    LWT.2023; 173: 114290.     CrossRef
  • The differences in carbohydrate utilization ability between six rounds of Sauce-flavor Daqu
    Qi Zhu, Liangqiang Chen, Zheng Peng, Qiaoling Zhang, Wanqiu Huang, Fan Yang, Guocheng Du, Juan Zhang, Li Wang
    Food Research International.2023; 163: 112184.     CrossRef
  • Microbial Community Affects Daqu Quality and the Production of Ethanol and Flavor Compounds in Baijiu Fermentation
    Pei-Jie Han, Lu-Jun Luo, Ying Han, Liang Song, Pan Zhen, Da-Yong Han, Yu-Hua Wei, Xin Zhou, Zhang Wen, Jun-Zhi Qiu, Feng-Yan Bai
    Foods.2023; 12(15): 2936.     CrossRef
  • Comparison of physicochemical characteristics and microbiome profiles of low-temperature Daqu with and without adding tartary buckwheat
    Jiamu Kang, Liangliang Jia, Zhongxiao Zhang, Min Zhang, Xiaoning Huang, Xiaoxue Chen, Bei-Zhong Han
    Food Bioscience.2022; 49: 101931.     CrossRef
  • What Are the Main Factors That Affect the Flavor of Sauce-Aroma Baijiu
    Jiao Niu, Shiqi Yang, Yi Shen, Wei Cheng, Hehe Li, Jinyuan Sun, Mingquan Huang, Baoguo Sun
    Foods.2022; 11(21): 3534.     CrossRef
  • Insights into the bacterial, fungal, and phage communities and volatile profiles in different types of Daqu
    Jiamu Kang, Xiaoxue Chen, Bei-Zhong Han, Yansong Xue
    Food Research International.2022; 158: 111488.     CrossRef
STATR: A simple analysis pipeline of Ribo-Seq in bacteria
Donghui Choe , Bernhard Palsson , Byung-Kwan Cho
J. Microbiol. 2020;58(3):217-226.   Published online January 28, 2020
DOI: https://doi.org/10.1007/s12275-020-9536-2
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AbstractAbstract
Gene expression changes in response to diverse environmental stimuli to regulate numerous cellular functions. Genes are expressed into their functional products with the help of messenger RNA (mRNA). Thus, measuring levels of mRNA in cells is important to understand cellular functions. With advances in next-generation sequencing (NGS), the abundance of cellular mRNA has been elucidated via transcriptome sequencing. However, several studies have found a discrepancy between mRNA abundance and protein levels induced by translational regulation, including different rates of ribosome entry and translational pausing. As such, the levels of mRNA are not necessarily a direct representation of the protein levels found in a cell. To determine a more precise way to measure protein expression in cells, the analysis of the levels of mRNA associated with ribosomes is being adopted. With an aid of NGS techniques, a single nucleotide resolution footprint of the ribosome was determined using a method known as Ribo- Seq or ribosome profiling. This method allows for the highthroughput measurement of translation in vivo, which was further analyzed to determine the protein synthesis rate, translational pausing, and cellular responses toward a variety of environmental changes. Here, we describe a simple analysis pipeline for Ribo-Seq in bacteria, so-called simple translatome analysis tool for Ribo-Seq (STATR). STATR can be used to carry out the primary processing of Ribo-Seq data, subsequently allowing for multiple levels of translatome study, from experimental validation to in-depth analyses. A command- by-command explanation is provided here to allow a broad spectrum of biologists to easily reproduce the analysis.

Citations

Citations to this article as recorded by  
  • Translation in Bacillus subtilis is spatially and temporally coordinated during sporulation
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    Nature Communications.2024;[Epub]     CrossRef
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    Microbiology and Biotechnology Letters.2021;[Epub]     CrossRef
  • RiboRid: A low cost, advanced, and ultra-efficient method to remove ribosomal RNA for bacterial transcriptomics
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    PLOS Genetics.2021; 17(9): e1009821.     CrossRef
  • Omics-based microbiome analysis in microbial ecology: from sequences to information
    Jang-Cheon Cho
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  • HRIBO: high-throughput analysis of bacterial ribosome profiling data
    Rick Gelhausen, Sarah L Svensson, Kathrin Froschauer, Florian Heyl, Lydia Hadjeras, Cynthia M Sharma, Florian Eggenhofer, Rolf Backofen, Valencia Alfonso
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    Dokyun Na
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Research Support, Non-U.S. Gov't
Functional Analysis of the Invariant Residue G791 of Escherichia coli 16S rRNA
Woo-Seok Song , Hong-Man Kim , Jae-Hong Kim , Se-Hoon Sim , Sang-Mi Ryou , Sanggoo Kim , Chang-Jun Cha , Philip R. Cunningham , Jeehyeon Bae , Kangseok Lee
J. Microbiol. 2007;45(5):418-421.
DOI: https://doi.org/2595 [pii]
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AbstractAbstract
The nucleotide at position 791(G791) of E. coli 16S rRNA was previously identified as an invariant residue for ribosomal function. In order to characterize the functional role of G791, base substitutions were introduced at this position, and mutant ribosomes were analyzed with regard to their protein synthesis ability, via the use of a specialized ribosome system. These ribosomal RNA mutations attenuated the ability of ribosomes to conduct protein synthesis by more than 65%. A transition mutation (G to A) exerted a moderate effect on ribosomal function, whereas a transversion mutation (G to C or U) resulted in a loss of protein synthesis ability of more than 90%. The sucrose gradient profiles of ribosomes and primer extension analysis showed that the loss of protein-synthesis ability of mutant ribosomes harboring a base substitution from G to U at position 791 stems partially from its inability to form 70S ribosomes. These findings show the involvement of the nucleotide at position 791 in the association of ribosomal subunits and protein synthesis steps after 70S formation, as well as the possibility of using 16S rRNA mutated at position 791 for the selection of second-site revertants in order to identify ligands that interact with G791 in protein synthesis.

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