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Superantigen SpeA attenuates the biofilm forming capacity of Streptococcus pyogenes
Anshu Babbar , Israel Barrantes , Dietmar H. Pieper , Andreas Itzek
J. Microbiol. 2019;57(7):626-636.   Published online June 27, 2019
DOI: https://doi.org/10.1007/s12275-019-8648-z
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  • 8 Web of Science
  • 9 Crossref
AbstractAbstract
Beta haemolytic Group A streptococcus (GAS) or Streptococcus pyogenes are strict human pathogens responsible for mild to severe fatal invasive infections. Even with enormous number of reports exploring the role of S. pyogenes exotoxins in its pathogenesis, inadequate knowledge on the biofilm process and the potential role of exotoxins in bacterial dissemination from matured biofilms has been a hindrance in development of effective and targeted treatments. Therefore, the present study was aimed in investigating the uncharted role of these exotoxins in biofilm process. Through our study the putative role of ciaRH in the SpeA dependent ablation of biofilm formation could be speculated and thus helping in bacterial dissemination. The seed-dispersal effect of SpeA was time and concentration dependent and seen to be consistent within various streptococcal species. Transcriptome analysis of SpeA treated S. pyogenes biofilms revealed the involvement of many transcriptional regulators (ciaRH) and response genes (luxS, shr, shp, SPy_0572), hinting towards specific mechanisms underlying the dispersal effect by SpeA. This finding opens up a discussion towards understanding a new mechanism involved in the pathogenesis of Streptococcus pyogenes and might help in understanding the bacterial infections in a better way.

Citations

Citations to this article as recorded by  
  • Pathomolecular epidemiology, antimicrobial resistance, and virulence genes of Streptococcus dysgalactiae subsp. equisimilis isolates from slaughtered pigs in India
    Sagar M Patel, Monalisa Sahoo, Jigarji Chaturji Thakor, Dinesh Murali, Pradeep Kumar, Rajendra Singh, Karam Pal Singh, G Saikumar, Chandrakanta Jana, Shailesh Kumar Patel, Akash B Mote, Ravichandran Karthikeyan, Rajesh Kumar Vandre, Jitendra Kumar Biswal,
    Journal of Applied Microbiology.2024;[Epub]     CrossRef
  • The involvement of CiaR and the CiaR-regulated serine protease HtrA in thermal adaptation of Streptococcus pneumoniae
    Ozcan Gazioglu, Medhanie Habtom, Peter W. Andrew, Hasan Yesilkaya
    Microbiology .2023;[Epub]     CrossRef
  • An Inventory of CiaR-Dependent Small Regulatory RNAs in Streptococci
    Nancy Jabbour, Marie-Frédérique Lartigue
    Frontiers in Microbiology.2021;[Epub]     CrossRef
  • Microbial biofilms and some aspects of anti-inflammatory drug use
    T. M. Rumynska, A. R. Hural, Y. T. Konechnyi, R. B. Vynnytska, A. V. Lozynskyi, Y. T. Salyha, O. P. Korniychuk, R.B. Lesyk
    Biopolymers and Cell.2021; 37(4): 247.     CrossRef
  • A current review of pathogenicity determinants of Streptococcus sp.
    P.S. Lannes‐Costa, J.S.S. Oliveira, G. Silva Santos, P.E. Nagao
    Journal of Applied Microbiology.2021; 131(4): 1600.     CrossRef
  • Genital Tract GAS Infection ISIDOG Guidelines
    Gilbert Donders, Peter Greenhouse, Francesca Donders, Ulrike Engel, Jorma Paavonen, Werner Mendling
    Journal of Clinical Medicine.2021; 10(9): 2043.     CrossRef
  • The Role and Regulatory Network of the CiaRH Two-Component System in Streptococcal Species
    Li-Yuan He, Yao-Jin Le, Zhong Guo, Sha Li, Xiao-Yan Yang
    Frontiers in Microbiology.2021;[Epub]     CrossRef
  • Deciphering Streptococcal Biofilms
    Puja Yadav, Shalini Verma, Richard Bauer, Monika Kumari, Meenakshi Dua, Atul Kumar Johri, Vikas Yadav, Barbara Spellerberg
    Microorganisms.2020; 8(11): 1835.     CrossRef
  • Dissecting Streptococcus pyogenes interaction with human
    Munazza Ijaz, Fuad Ameen, Yaseen Abd Alfoteih, Saba Shamim, Wafa A. Alshehri, Ghulam Murtaza
    Archives of Microbiology.2020; 202(8): 2023.     CrossRef
Research Support, Non-U.S. Gov't
Comparative Analysis of Immune Responses to Mycobacterium abscessus Infection and Its Antigens in Two Murine Models
Bo-Young Jeon , Jeongyeon Kwak , Seung-Sub Lee , SangNae Cho , Chul Jae Won , Jin Man Kim , Sung Jae Shin
J. Microbiol. 2009;47(5):633-640.   Published online October 24, 2009
DOI: https://doi.org/10.1007/s12275-009-0139-1
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  • 10 Crossref
AbstractAbstract
Mycobacterium abscessus has been identified as an emerging pulmonary pathogen in humans. Because little is known regarding immune responses elicited by M. abscessus or its antigens, immunological responses were studied in two murine models subjected to intravenous (high-dose or systemic infection) or pulmonary (low-dose or local infection) inoculation with M. abscessus ATCC 19977. An overall comparison between the two models showed similar patterns of bacterial survival and host immune responses. The colonization of M. abscessus was the highest at 5 days post-infection (dpi) and its elimination was positively correlated with cell-mediated immunity in both challenges. However, an inverse relationship was observed between progressive inflammation and mycobacterial colonization levels in mice infected with a high dose at 14 dpi. Regarding antigens, culture filtrate (CF) of M. abscessus strongly induced IFN-γ secretion, whereas cellular extract (CE) antigen elicited strong antibody responses. The antibody response to M. abscessus antigens in mice subjected to low-dose infection increased when the cellular immune response decreased over 14 dpi. However, the antibody response for the high-dose infection increased promptly after the infection. In comparison of cytokine expression in lung homogenates after M. abscessus infection, Th1 and Th2 cytokines increased simultaneously in the high-dose infection, whereas only cell-mediated immunity developed in the low-dose pulmonary infection. These findings not only enhance our understanding of the immune response to M. abscessus infection according to systemic or pulmonary infection, but may also aid in immunological diagnosis and vaccine development.

Citations

Citations to this article as recorded by  
  • Mycobacterium abscessus biofilm cleared from murine lung by monoclonal antibody against bacterial DNABII proteins
    Joseph A. Jurcisek, Nikola Kurbatfinski, Kathryn Q. Wilbanks, Jaime D. Rhodes, Steven D. Goodman, Lauren O. Bakaletz
    Journal of Cystic Fibrosis.2025; 24(2): 374.     CrossRef
  • Virulence Mechanisms of Mycobacterium abscessus: Current Knowledge and Implications for Vaccine Design
    Kia C. Ferrell, Matt D. Johansen, James A. Triccas, Claudio Counoupas
    Frontiers in Microbiology.2022;[Epub]     CrossRef
  • Vaccination inducing durable and robust antigen-specific Th1/Th17 immune responses contributes to prophylactic protection against Mycobacterium avium infection but is ineffective as an adjunct to antibiotic treatment in chronic disease
    Ju Mi Lee, Jiyun Park, Steven G Reed, Rhea N Coler, Jung Joo Hong, Lee-Han Kim, Wonsik Lee, Kee Woong Kwon, Sung Jae Shin
    Virulence.2022; 13(1): 808.     CrossRef
  • Species-Specific Interferon-Gamma Release Assay for the Diagnosis of Mycobacterium abscessus Complex Infection
    Mathis Steindor, Florian Stehling, Margarete Olivier, Jan Kehrmann, Margo Diricks, Florian P. Maurer, Peter A. Horn, Svenja Straßburg, Matthias Welsner, Sivagurunathan Sutharsan, Monika Lindemann
    Frontiers in Microbiology.2021;[Epub]     CrossRef
  • A New Model of Chronic Mycobacterium abscessus Lung Infection in Immunocompetent Mice
    Camilla Riva, Enrico Tortoli, Federica Cugnata, Francesca Sanvito, Antonio Esposito, Marco Rossi, Anna Colarieti, Tamara Canu, Cristina Cigana, Alessandra Bragonzi, Nicola Ivan Loré, Paolo Miotto, Daniela Maria Cirillo
    International Journal of Molecular Sciences.2020; 21(18): 6590.     CrossRef
  • Mycobacterium abscessus Morphotype Comparison in a Murine Model
    Lindsay J. Caverly, Silvia M. Caceres, Cori Fratelli, Carrie Happoldt, Kelley M. Kidwell, Kenneth C. Malcolm, Jerry A. Nick, David P. Nichols, Nades Palaniyar
    PLOS ONE.2015; 10(2): e0117657.     CrossRef
  • Increasing nontuberculous mycobacteria infection in cystic fibrosis
    Ophir Bar-On, Huda Mussaffi, Meir Mei-Zahav, Dario Prais, Guy Steuer, Patrick Stafler, Shai Hananya, Hannah Blau
    Journal of Cystic Fibrosis.2015; 14(1): 53.     CrossRef
  • Differential Immune Responses to Segniliparus rotundus and Segniliparus rugosus Infection and Analysis of Their Comparative Virulence Profiles
    Jong-Seok Kim, Woo Sik Kim, Keehoon Lee, Choul-Jae Won, Jin Man Kim, Seok-Yong Eum, Won-Jung Koh, Sung Jae Shin, Yung-Fu Chang
    PLoS ONE.2013; 8(3): e59646.     CrossRef
  • Mycobacterium abscessus Bacteremia After Receipt of Intravenous Infusate of Cytokine-Induced Killer Cell Therapy for Body Beautification and Health Boosting
    Raymond Liu, Kelvin K. W. To, Jade L. L. Teng, Garnet K. Y. Choi, Ka-Yi Mok, Kin-Ip Law, Eugene Y. K. Tso, Kitty S. C. Fung, Tak-Chiu Wu, Alan K. L. Wu, Shing-Hoi Fung, Sally C. Y. Wong, Nigel J. Trendell-Smith, Kwok-Yung Yuen
    Clinical Infectious Diseases.2013; 57(7): 981.     CrossRef
  • Current Understanding ofMycobacterium abscessusInfection
    Go-Eun Choi, Youngsuk Jo, Sung Jae Shin
    Journal of Bacteriology and Virology.2012; 42(1): 17.     CrossRef

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