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Vaginal Microbiome Dysbiosis is Associated with the Different Cervical Disease Status
Yingying Ma , Yanpeng Li , Yanmei Liu , Le Cao , Xiao Han , Shujun Gao , Chiyu Zhang
J. Microbiol. 2023;61(4):423-432.   Published online April 3, 2023
DOI: https://doi.org/10.1007/s12275-023-00039-3
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AbstractAbstract
Vaginal microbiome composition was demonstrated to be associated with cervical disease. The colonization characteristics of vaginal microbes and their association with the different cervical disease status, especially cervical cancer (CC), are rarely investigated. In this cross-sectional study, we characterized the vaginal microbiome of women with different status of cervical diseases, including 22 NV + (normal tissue with HPV infection), low-grade squamous intraepithelial lesion (LSIL, n = 45), high-grade squamous intraepithelial lesion (HSIL, n = 36) and CC (n = 27) using bacterial 16S DNA sequencing. Thirty HPV-negative women with normal tissue were used as the control group. We found that higher diversity of microbiome with gradual depletion of Lactobacillus, especially L. crispatus, was associated with the severity of cervical disease. High-risk HPV16 infection was associated with higher microbiome diversity and depletion of Lactobacillus in high-grade cervical diseases (i.e. HSIL and CC). The CC group was characterized by higher levels of Fannyhessea vaginae, Prevotella, Bacteroides, Finegoldia, Vibrio, Veillonella, Peptostreptococcus, and Dialister. Co-occurrence network analyses showed that negative correlations were exclusively observed between Lactobacillus and other bacteria, and almost all non-Lactobacillus bacteria were positively correlated with each other. In particular, the most diverse and complex co-occurrence network of vaginal bacteria, as well as a complete loss of L. crispatus, was observed in women with CC. Logistic regression model identified HPV16 and Lactobacillus as significant risk and protective factors for CC, respectively. These results suggest that specific Lactobacillus species (e.g. L. crispatus and L. iners) can be used as important markers to target prevention measures prioritizing HPV16-infected women and other hrHPV-infected women for test, vaccination and treat initiatives.

Citations

Citations to this article as recorded by  
  • Vaginal Microbiome and Pregnancy Complications: A Review
    Angeliki Gerede, Konstantinos Nikolettos, Eleftherios Vavoulidis, Chrysoula Margioula-Siarkou, Stamatios Petousis, Maria Giourga, Panagiotis Fotinopoulos, Maria Salagianni, Sofoklis Stavros, Konstantinos Dinas, Nikolaos Nikolettos, Ekaterini Domali
    Journal of Clinical Medicine.2024; 13(13): 3875.     CrossRef
  • Advancements in the Vaginal Microenvironment and Regression of High-Risk Human Papillomavirus
    Na He, Cunjian Yi, Qingsong Zeng, Wumei Jing, Wenrong He
    Indian Journal of Microbiology.2024;[Epub]     CrossRef
  • Research Progress on Related Factors of Cervical High-Grade Squamous Intraepithelial Lesions
    红颖 王
    Advances in Clinical Medicine.2023; 13(12): 20536.     CrossRef
  • Role of the vaginal microbiome in miscarriage: exploring the relationship
    Marwa Saadaoui, Parul Singh, Osman Ortashi, Souhaila Al Khodor
    Frontiers in Cellular and Infection Microbiology.2023;[Epub]     CrossRef
Reovirus safety study for proliferation and differentiation of human adipose-derived mesenchymal stem cells
Jeong-Soo Park , Manbok Kim
J. Microbiol. 2017;55(1):75-79.   Published online December 30, 2016
DOI: https://doi.org/10.1007/s12275-017-6542-0
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  • 8 Crossref
AbstractAbstract
Naturally occurring reoviruses are live replication-proficient viruses specifically infecting human cancer cells while sparing the normal counterparts. Stem cells can be highly susceptible to viral infection due to their innate high proliferation potential and other active signaling pathways of cells that might be involved in viral tropism. In the previous study, we showed that reoviruses could adversely affect murine embryonic stem cells’ integrity in vitro and in vivo. Oncolytic viruses, delivered systemically face many hurdles that also impede their localization and infection of, metastatic tumors, due to a variety of immune and physical barriers. To overcome such hurdles to systemic delivery, several studies supported the idea that certain types of cells, including mesenchymal stem cells, might play a role as cell carriers for oncolytic viruses. Thus, it would be interesting to examine whether human adult stem cells such as human adipose-derived mesenchymal stem cells could be saved by the reoviral challenge. In this study, we report that biological activities such as proliferation and multipotency of human adipose-derived stem cells are not affected by wild-type reovirus challenge as evidenced by survival, osteogenic and adipogenic differentiation potential assays following treatment with reoviruses. Therefore, unlike murine embryonic stem cells, our study strongly suggests that human adipose-derived adult stem cells could be spared in vivo during wild-type reoviral anti-cancer therapeutics in a clinical setting. Furthermore, the results support the possible clinical use of human adipose-derived stem cells as an effective cell carrier of oncolytic reovirus to maximize their tumor tropism and anti-tumor activity.

Citations

Citations to this article as recorded by  
  • Modulation of Reoviral Cytolysis (II): Cellular Stemness
    Tarryn Bourhill, Leili Rohani, Mehul Kumar, Pinaki Bose, Derrick Rancourt, Randal N. Johnston
    Viruses.2023; 15(7): 1473.     CrossRef
  • Mesenchymal stem cell carriers enhance antitumor efficacy induced by oncolytic reovirus in acute myeloid leukemia
    Xianyao Wang, Yichen Yang, Nianxue Wang, Xijun Wu, Jianwei Xu, Yanhua Zhou, Xing Zhao, Zhixu He
    International Immunopharmacology.2021; 94: 107437.     CrossRef
  • Mesenchymal stem cells support delivery and boost the efficacy of oncolytic reoviruses in TC‐1 tumor cells
    Razieh S. Banijamali, Hoorieh Soleimanjahi, Sara Soudi, Hesam Karimi
    Journal of Cellular Biochemistry.2021; 122(10): 1360.     CrossRef
  • Mesenchymal stem cells as carriers for systemic delivery of oncolytic viruses
    Agata Hadryś, Aleksander Sochanik, Grant McFadden, Joanna Jazowiecka-Rakus
    European Journal of Pharmacology.2020; 874: 172991.     CrossRef
  • Recent advances in targeting cancer stem cells using oncolytic viruses
    You-Ni Zhang, Shi-Bing Wang, Shu-Shu Song, Pei-Yang Hu, Yu-Cheng Zhou, Yi-Ping Mou, Xiao-Zhou Mou
    Biotechnology Letters.2020; 42(6): 865.     CrossRef
  • The oncolytic efficacy and safety of avian reovirus and its dynamic distribution in infected mice
    Ruimin Cai, Guangyuan Meng, Yi Li, Wenyang Wang, Youxiang Diao, Shuping Zhao, Qiang Feng, Yi Tang
    Experimental Biology and Medicine.2019; 244(12): 983.     CrossRef
  • Going (Reo)Viral: Factors Promoting Successful Reoviral Oncolytic Infection
    Tarryn Bourhill, Yoshinori Mori, Derrick Rancourt, Maya Shmulevitz, Randal Johnston
    Viruses.2018; 10(8): 421.     CrossRef
  • Primary lymphocyte infection models for KSHV and its putative tumorigenesis mechanisms in B cell lymphomas
    Sangmin Kang, Jinjong Myoung
    Journal of Microbiology.2017; 55(5): 319.     CrossRef

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