Journal Article
- Superantigen SpeA attenuates the biofilm forming capacity of Streptococcus pyogenes
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Anshu Babbar , Israel Barrantes , Dietmar H. Pieper , Andreas Itzek
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J. Microbiol. 2019;57(7):626-636. Published online June 27, 2019
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DOI: https://doi.org/10.1007/s12275-019-8648-z
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Abstract
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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.
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Citations
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- Pathomolecular epidemiology, antimicrobial resistance, and virulence genes of Streptococcus dysgalactiae subsp. equisimilis isolates from slaughtered pigs in India
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Ozcan Gazioglu, Medhanie Habtom, Peter W. Andrew, Hasan Yesilkaya
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Nancy Jabbour, Marie-Frédérique Lartigue
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T. M. Rumynska, A. R. Hural, Y. T. Konechnyi, R. B. Vynnytska, A. V. Lozynskyi, Y. T. Salyha, O. P. Korniychuk, R.B. Lesyk
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A current review of pathogenicity determinants of
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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
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Microorganisms.2020; 8(11): 1835. CrossRef - Dissecting Streptococcus pyogenes interaction with human
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Research Support, Non-U.S. Gov't
- Comparative Analysis of Immune Responses to Mycobacterium abscessus Infection and Its Antigens in Two Murine Models
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Bo-Young Jeon , Jeongyeon Kwak , Seung-Sub Lee , SangNae Cho , Chul Jae Won , Jin Man Kim , Sung Jae Shin
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J. Microbiol. 2009;47(5):633-640. Published online October 24, 2009
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DOI: https://doi.org/10.1007/s12275-009-0139-1
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48
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Abstract
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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.
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Citations
Citations to this article as recorded by

- Mycobacterium abscessus biofilm cleared from murine lung by monoclonal antibody against bacterial DNABII proteins
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