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Review
Influence of Microbiota on Vaccine Effectiveness: “Is the Microbiota the Key to Vaccine‑induced Responses?”
So-Hee Hong
J. Microbiol. 2023;61(5):483-494.   Published online April 13, 2023
DOI: https://doi.org/10.1007/s12275-023-00044-6
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  • 12 Web of Science
  • 11 Crossref
AbstractAbstract
Vaccines are one of the most powerful tools for preventing infectious diseases. To effectively fight pathogens, vaccines should induce potent and long-lasting immune responses that are specific to the pathogens. However, not all vaccines can induce effective immune responses, and the responses vary greatly among individuals and populations. Although several factors, such as age, host genetics, nutritional status, and region, affect the effectiveness of vaccines, increasing data have suggested that the gut microbiota is critically associated with vaccine-induced immune responses. In this review, I discuss how gut microbiota affects vaccine effectiveness based on the clinical and preclinical data, and summarize possible underlying mechanisms related to the adjuvant effects of microbiota. A better understanding of the link between vaccine-induced immune responses and the gut microbiota using high-throughput technology and sophisticated system vaccinology approaches could provide crucial insights for designing effective personalized preventive and therapeutic vaccination strategies.

Citations

Citations to this article as recorded by  
  • Antibiotic-mediated dysbiosis leads to activation of inflammatory pathways
    Jemma J. Taitz, Jian Tan, Duan Ni, Camille Potier-Villette, Georges Grau, Ralph Nanan, Laurence Macia
    Frontiers in Immunology.2025;[Epub]     CrossRef
  • Intestinal Microbiota and Its Effect on Vaccine-Induced Immune Amplification and Tolerance
    Yixin Liu, Jianfeng Zhou, Yushang Yang, Xiangzheng Chen, Longqi Chen, Yangping Wu
    Vaccines.2024; 12(8): 868.     CrossRef
  • Immune Cells, Gut Microbiota, and Vaccines: A Gender Perspective
    Pierluigi Rio, Mario Caldarelli, Monica Chiantore, Francesca Ocarino, Marcello Candelli, Antonio Gasbarrini, Giovanni Gambassi, Rossella Cianci
    Cells.2024; 13(6): 526.     CrossRef
  • Parasite-microbiota interactions: a pathway to innovative interventions for Chagas disease, leishmaniasis, and ascariasis
    Juan David Ramírez, Sergio Castañeda, Jill Weatherhead, Cristina Poveda
    Future Microbiology.2024; : 1.     CrossRef
  • Ruhao Dashi granules exert therapeutic effects on H1N1 influenza virus infection by altering intestinal microflora composition
    Wei Pan, Rui Wu, Qianyun Zhang, Yuan Ma, Jinxiang Xiang, Jingbo Wang, Jing Chen
    Frontiers in Microbiology.2024;[Epub]     CrossRef
  • When inflammatory stressors dramatically change, disease phenotypes may transform between autoimmune hematopoietic failure and myeloid neoplasms
    Xi-Chen Zhao, Bo Ju, Nuan-Nuan Xiu, Xiao-Yun Sun, Fan-Jun Meng
    Frontiers in Immunology.2024;[Epub]     CrossRef
  • Long Prime–Boost Interval and Heightened Anti-GD2 Antibody Response to Carbohydrate Cancer Vaccine
    Irene Y. Cheung, Audrey Mauguen, Shakeel Modak, Ellen M. Basu, Yi Feng, Brian H. Kushner, Nai Kong Cheung
    Vaccines.2024; 12(6): 587.     CrossRef
  • Baseline Gut Microbiota Was Associated with Long-Term Immune Response at One Year Following Three Doses of BNT162b2
    Li-Na Zhang, Jing-Tong Tan, Ho-Yu Ng, Yun-Shi Liao, Rui-Qi Zhang, Kwok-Hung Chan, Ivan Fan-Ngai Hung, Tommy Tsan-Yuk Lam, Ka-Shing Cheung
    Vaccines.2024; 12(8): 916.     CrossRef
  • Immunologische Konsequenzen bei frühgeborenen Kindern
    Josina M. Hofer, Dimitra E. Zazara, Anke Diemert, Petra Clara Arck
    Gynäkologische Endokrinologie.2023; 21(4): 261.     CrossRef
  • Ginsenoside Rb1 enhanced immunity and altered the gut microflora in mice immunized by H1N1 influenza vaccine
    Chuanqi Wan, Rufeng Lu, Chen Zhu, Haibo Wu, Guannan Shen, Yang Yang, Xiaowei Wu, Bangjiang Fang, Yuzhou He
    PeerJ.2023; 11: e16226.     CrossRef
  • Factors Influencing Microbiota in Modulating Vaccine Immune Response: A Long Way to Go
    Francesca Romana Ponziani, Gaetano Coppola, Pierluigi Rio, Mario Caldarelli, Raffaele Borriello, Giovanni Gambassi, Antonio Gasbarrini, Rossella Cianci
    Vaccines.2023; 11(10): 1609.     CrossRef
Journal Article
Construction of a genetic linkage map and QTL mapping of agronomic traits in Auricularia auricula-judae
Li-Xin Lu , Fang-Jie Yao , Peng Wang , Ming Fang , You-Min Zhang , Wei-Tong Zhang , Xiang-Hui Kong , Jia Lu
J. Microbiol. 2017;55(10):792-799.   Published online September 28, 2017
DOI: https://doi.org/10.1007/s12275-017-7241-6
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  • 13 Crossref
AbstractAbstract
Auricularia auricula-judae is a traditional edible fungus that is cultivated widely in China. In this study, a genetic linkage map for A. auricula-judae was constructed using a mapping population consisting of 138 monokaryons derived from a hybrid strain (A119-5). The monokaryotic parent strains A14-5 and A18-119 were derived from two cultivated varieties, A14 (Qihei No. 1) and A18 (Qihei No. 2), respectively. In total, 130 simple sequence repeat markers were mapped. These markers were developed using the whole genome sequence of A. auricula-judae and amplified in A14-5, A18- 119, and the mapping population. The map consisted of 11 linkage groups (LGs) spanning 854 cM, with an average interval length of 6.57 cM. A testcross population was derived from crossing between the monokaryon A184-57 (from the wild strain A184 as a tester strain) and the mapping population. Important agronomic trait-related QTLs, including mycelium growth rate on potato dextrose agar for the mapping population, mycelium growth rate on potato dextrose agar and sawdust for the testcross population, growth period (days from inoculation to fruiting body harvesting), and yield for the testcross population, were identified using the composite interval mapping method. Six mycelium growth raterelated QTLs were identified on LG1 and LG4, two growth period-related QTLs were identified on LG2, and three yieldrelated QTLs were identified on LG2 and LG6. The results showed no linkage relationship between mycelium growth rate and growth period. The present study provides a foundation for locating genes for important agronomic characteristics in A. auricula-judae in the future.

Citations

Citations to this article as recorded by  
  • Exploring the potential of black fungus, Auricularia auricula, as a feed additive in African catfish, Clarias gariepinus, farming
    Lee Seong Wei, Alvin Amos Adrian Susin, Albaris B. Tahiluddin, Liew Vui Kien, Wendy Wee
    Heliyon.2024; 10(13): e33810.     CrossRef
  • Evaluation of Drought Tolerance and Trehalose Response in Auricularia heimuer
    Jian Sun, Fangjie Yao, Lixin Lu, Youmin Zhang, Ming Fang, Xiaoxu Ma, Kaisheng Shao, Xu Sun
    Horticulturae.2024; 10(12): 1312.     CrossRef
  • Medicinal Value, Genetic Diversity, and Genetic Relationship Analysis of Auricularia cornea (Agaricomycetes) Based on ITS, ISSR, and SRAP Markers
    Ping Du, Hong-Yan He, Ni-Ya Wu, Tianxu Cao, Bao-Kai Cui
    International Journal of Medicinal Mushrooms.2024; 26(5): 43.     CrossRef
  • Velvet Family Members Regulate Pigment Synthesis of the Fruiting Bodies of Auricularia cornea
    Xiaoxu Ma, Lixin Lu, Youmin Zhang, Ming Fang, Kaisheng Shao, Xu Sun, Fangjie Yao, Peng Wang
    Journal of Fungi.2023; 9(4): 412.     CrossRef
  • The polysaccharides from Auricularia auricula alleviate non-alcoholic fatty liver disease via modulating gut microbiota and bile acids metabolism
    Yifan Shu, Yujie Huang, Wei Dong, Xia Fan, Yi Sun, Guijie Chen, Xiaoxiong Zeng, Hong Ye
    International Journal of Biological Macromolecules.2023; 246: 125662.     CrossRef
  • Detection of quantitative trait loci underlying fruiting body and yield-related traits in Hericium erinaceus
    Wenbing Gong, Xiaoya Song, Chunliang Xie, Yingjun Zhou, Zuohua Zhu, Chao Xu, Yuande Peng
    Scientia Horticulturae.2022; 293: 110729.     CrossRef
  • Analysis of the Genome Sequence of Strain GiC-126 of Gloeostereum incarnatum with Genetic Linkage Map
    Wan-Zhu Jiang, Fang-Jie Yao, Ming Fang, Li-Xin Lu, You-Min Zhang, Peng Wang, Jing-Jing Meng, Jia Lu, Xiao-Xu Ma, Qi He, Kai-Sheng Shao, Asif Ali Khan, Yun-Hui Wei
    Mycobiology.2021; 49(4): 406.     CrossRef
  • SNP-Based Genetic Linkage Map and Quantitative Trait Locus Mapping Associated with the Agronomically Important Traits of Hypsizygus marmoreus
    Youn-Lee Oh, In-Geol Choi, Kab-Yeul Jang, Min-Seek Kim, Min ji Oh, Ji-Hoon Im
    Mycobiology.2021; 49(6): 589.     CrossRef
  • Genetic linkage map construction and quantitative trait loci mapping of agronomic traits in Gloeostereum incarnatum
    Wan-Zhu Jiang, Fang-Jie Yao, Li-Xin Lu, Ming Fang, Peng Wang, You-Min Zhang, Jing-Jing Meng, Jia Lu, Xiao-Xu Ma, Qi He, Kai-Sheng Shao
    Journal of Microbiology.2021; 59(1): 41.     CrossRef
  • Polysaccharides from Auricularia auricula: Preparation, structural features and biological activities
    Nana Chen, Hao Zhang, Xin Zong, Siyu Li, Jiaojiao Wang, Yizhen Wang, Mingliang Jin
    Carbohydrate Polymers.2020; 247: 116750.     CrossRef
  • Genome Sequence Analysis of Auricularia heimuer Combined with Genetic Linkage Map
    Ming Fang, Xiaoe Wang, Ying Chen, Peng Wang, Lixin Lu, Jia Lu, Fangjie Yao, Youmin Zhang
    Journal of Fungi.2020; 6(1): 37.     CrossRef
  • A Resequencing-Based Ultradense Genetic Map of Hericium erinaceus for Anchoring Genome Sequences and Identifying Genetic Loci Associated With Monokaryon Growth
    Wenbing Gong, Chunliang Xie, Yingjun Zhou, Zuohua Zhu, Yahui Wang, Yuande Peng
    Frontiers in Microbiology.2020;[Epub]     CrossRef
  • Comparative transcriptome analysis reveals relationship of three major domesticated varieties of Auricularia auricula-judae
    Yuhui Zhao, Liang Wang, Dongshan Zhang, Rong Li, Tianyou Cheng, Yibi Zhang, Xueju Liu, Gary Wong, Yuguo Tang, Hui Wang, Shan Gao
    Scientific Reports.2019;[Epub]     CrossRef

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