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Year 2019, Volume: 9 Issue: 1, 49 - 52, 29.03.2019
https://doi.org/10.5152/clinexphealthsci.2018.1079

Abstract

References

  • [1] Edwards MS, Baker CJ. Streptococcus agalactiae (Group B Streptococcus). Mandell GL, Bennett JE, Dolin R, editors. Mandell, Douglas, and Bennett’s Principles and Practice of Infectious Diseases. 7th ed. Philadelphia: Churchill, Livingston, Elsevier; 2009;2655–663.
  • [2] Schuchat A. Epidemiology of group B streptococcal disease in the United States: shifting paradigms. Clin Microbiol Rev 1998; 11:497-513.
  • [3] Jones N, Oliver K, Jones Y, Haines A, Crook D. Carriage of group B streptococcus in pregnant women from Oxford, UK. J Clin Pathol 2006; 59:363-66.
  • [4] Yılmaz Karadağ F, Hızel K, Gelişen O. Colonization of Group B Streptococci In Pregnant Women At Delivery. J Turk Soc Obstet Gynecol 2013; 10:16-20.
  • [5] Landwehr-Kenzel S, Henneke P. Interaction of Streptococcus agalactiae and Cellular Innate Immunity in Colonization and Disease. Front Immunol 2014; 29:519.
  • [6] Rajagopal L. Understanding the regulation of Group B Streptococcal virulence factors. Future Microbiol 2009; 4:201- 21.
  • [7] Rubens CE, Wessels MR, Heggen LM, Kasper DL. Transposon mutagenesis of type III group B Streptococcus: correlation of capsule expression with virulence. Proc Natl Acad Sci USA 1987; 84:7208-12.
  • [8] Vornhagen J, Adams Waldorf KM, Rajagopal L. Perinatal Group B Streptococcal Infections: Virulence Factors, Immunity, and Prevention Strategies. Trends Microbiol 2017; 25: 919-931.
  • [9] Doerflinger SY, Throop AL, Herbst-Kralovetz MM. Bacteria in the vaginal microbiome alter the innate immune response and barrier properties of the human vaginal epithelia in a speciesspecific manner. J Infect Dis 2014; 209:1989-99.
  • [10] Palomino DC, Marti LC. Chemokines and immunity. Einstein (Sao Paulo) 2015; 13:469-73.
  • [11] Mukaida N, Harada A, Yasumoto K, Matsushima K. Properties of pro-inflammatory cell type-specific leukocyte chemotactic cytokines, Interleukin 8 (IL-8) and monocyte chemotactic and activating factor (MCAF). Microbiol Immunol 1992; 36:773-89.
  • [12] Guttormsen HK, Baker CJ, Edwards MS, Paoletti LC, Kasper DL. Quantitative determination of antibodies to type III group B streptococcal polysaccharide. J Infect Dis 1996; 173: 142-50.
  • [13] Vallejo JG, Baker CJ, Edwards MS. Interleukin-6 production by human neonatal monocytes stimulated by type III group B streptococci. J Infect Dis 1996; 174:332-37.
  • [14] Williams PA, Bohnsack JF, Augustine NH, Drummond WK, Rubens CE, Hill HR. Production of tumor necrosis factor by human cells in vitro and in vivo induced by group B streptococci. J Pediatr 1993; 123:292-300.
  • [15] Vallejo JG, Baker CJ, Edwards MS. Roles of the bacterial cell wall and capsule in induction of tumor necrosis factor alpha by type III group B streptococci. Infect Immun 1996; 64:5042-46.
  • [16] Maisey HC, Doran KS, Nizet V. Recent advances in understanding the molecular basis of group B Streptococcus virulence. Expert Rev Mol Med 2008; 22:10:e27.

Group B Streptococci Induce Interleukin 8 Production in Human Cervical Epithelial Cell Cultures: The Role of Capsule Polysaccharide

Year 2019, Volume: 9 Issue: 1, 49 - 52, 29.03.2019
https://doi.org/10.5152/clinexphealthsci.2018.1079

Abstract

Objective: Group B streptococci (GBS) are the major cause of pneumonia, sepsis, and meningitis in neonates and adults. Epithelial invasion and
early cytokine response of female genital tract considered to be important in the pathogenesis of GBS infection. In this study, we studied the IL-8
induction in cervical epithelial cells in response to stimulus with encapsulated (COH1) and unencapsulated (COH1-13) strains of group B streptococci.
Methods: Human cervical epithelial cancer cell (HeLa) cultures were stimulated with different concentrations (106 CFU/ml and 108 CFU/ml) of two
GBS strains. E.coli LPS was used as positive control and at specified time points (4, 8 and 24 hour) cell culture supernatant samples were collected.
IL-8 level in samples was quantified by using ELISA assay.
Results: Both GBS strains caused an equal IL-8 response in HeLa cells in a time-dependent manner. In addition, cytokine levels triggered by different
bacterial concentrations were similar and comparable with LPS.
Conclusion: Our study showed that GBS induce proinflammatory IL-8 levels in cervix epithelial cells. This induction seems to be independent from
capsule polysaccharides and suggesting that other bacterial components are involved in IL-8 stimulation.

References

  • [1] Edwards MS, Baker CJ. Streptococcus agalactiae (Group B Streptococcus). Mandell GL, Bennett JE, Dolin R, editors. Mandell, Douglas, and Bennett’s Principles and Practice of Infectious Diseases. 7th ed. Philadelphia: Churchill, Livingston, Elsevier; 2009;2655–663.
  • [2] Schuchat A. Epidemiology of group B streptococcal disease in the United States: shifting paradigms. Clin Microbiol Rev 1998; 11:497-513.
  • [3] Jones N, Oliver K, Jones Y, Haines A, Crook D. Carriage of group B streptococcus in pregnant women from Oxford, UK. J Clin Pathol 2006; 59:363-66.
  • [4] Yılmaz Karadağ F, Hızel K, Gelişen O. Colonization of Group B Streptococci In Pregnant Women At Delivery. J Turk Soc Obstet Gynecol 2013; 10:16-20.
  • [5] Landwehr-Kenzel S, Henneke P. Interaction of Streptococcus agalactiae and Cellular Innate Immunity in Colonization and Disease. Front Immunol 2014; 29:519.
  • [6] Rajagopal L. Understanding the regulation of Group B Streptococcal virulence factors. Future Microbiol 2009; 4:201- 21.
  • [7] Rubens CE, Wessels MR, Heggen LM, Kasper DL. Transposon mutagenesis of type III group B Streptococcus: correlation of capsule expression with virulence. Proc Natl Acad Sci USA 1987; 84:7208-12.
  • [8] Vornhagen J, Adams Waldorf KM, Rajagopal L. Perinatal Group B Streptococcal Infections: Virulence Factors, Immunity, and Prevention Strategies. Trends Microbiol 2017; 25: 919-931.
  • [9] Doerflinger SY, Throop AL, Herbst-Kralovetz MM. Bacteria in the vaginal microbiome alter the innate immune response and barrier properties of the human vaginal epithelia in a speciesspecific manner. J Infect Dis 2014; 209:1989-99.
  • [10] Palomino DC, Marti LC. Chemokines and immunity. Einstein (Sao Paulo) 2015; 13:469-73.
  • [11] Mukaida N, Harada A, Yasumoto K, Matsushima K. Properties of pro-inflammatory cell type-specific leukocyte chemotactic cytokines, Interleukin 8 (IL-8) and monocyte chemotactic and activating factor (MCAF). Microbiol Immunol 1992; 36:773-89.
  • [12] Guttormsen HK, Baker CJ, Edwards MS, Paoletti LC, Kasper DL. Quantitative determination of antibodies to type III group B streptococcal polysaccharide. J Infect Dis 1996; 173: 142-50.
  • [13] Vallejo JG, Baker CJ, Edwards MS. Interleukin-6 production by human neonatal monocytes stimulated by type III group B streptococci. J Infect Dis 1996; 174:332-37.
  • [14] Williams PA, Bohnsack JF, Augustine NH, Drummond WK, Rubens CE, Hill HR. Production of tumor necrosis factor by human cells in vitro and in vivo induced by group B streptococci. J Pediatr 1993; 123:292-300.
  • [15] Vallejo JG, Baker CJ, Edwards MS. Roles of the bacterial cell wall and capsule in induction of tumor necrosis factor alpha by type III group B streptococci. Infect Immun 1996; 64:5042-46.
  • [16] Maisey HC, Doran KS, Nizet V. Recent advances in understanding the molecular basis of group B Streptococcus virulence. Expert Rev Mol Med 2008; 22:10:e27.
There are 16 citations in total.

Details

Primary Language English
Subjects Health Care Administration
Journal Section Articles
Authors

Burak Aksu This is me 0000-0002-3439-9158

Özgür Yanılmaz This is me 0000-0003-3847-7288

Publication Date March 29, 2019
Submission Date February 6, 2018
Published in Issue Year 2019 Volume: 9 Issue: 1

Cite

APA Aksu, B., & Yanılmaz, Ö. (2019). Group B Streptococci Induce Interleukin 8 Production in Human Cervical Epithelial Cell Cultures: The Role of Capsule Polysaccharide. Clinical and Experimental Health Sciences, 9(1), 49-52. https://doi.org/10.5152/clinexphealthsci.2018.1079
AMA Aksu B, Yanılmaz Ö. Group B Streptococci Induce Interleukin 8 Production in Human Cervical Epithelial Cell Cultures: The Role of Capsule Polysaccharide. Clinical and Experimental Health Sciences. March 2019;9(1):49-52. doi:10.5152/clinexphealthsci.2018.1079
Chicago Aksu, Burak, and Özgür Yanılmaz. “Group B Streptococci Induce Interleukin 8 Production in Human Cervical Epithelial Cell Cultures: The Role of Capsule Polysaccharide”. Clinical and Experimental Health Sciences 9, no. 1 (March 2019): 49-52. https://doi.org/10.5152/clinexphealthsci.2018.1079.
EndNote Aksu B, Yanılmaz Ö (March 1, 2019) Group B Streptococci Induce Interleukin 8 Production in Human Cervical Epithelial Cell Cultures: The Role of Capsule Polysaccharide. Clinical and Experimental Health Sciences 9 1 49–52.
IEEE B. Aksu and Ö. Yanılmaz, “Group B Streptococci Induce Interleukin 8 Production in Human Cervical Epithelial Cell Cultures: The Role of Capsule Polysaccharide”, Clinical and Experimental Health Sciences, vol. 9, no. 1, pp. 49–52, 2019, doi: 10.5152/clinexphealthsci.2018.1079.
ISNAD Aksu, Burak - Yanılmaz, Özgür. “Group B Streptococci Induce Interleukin 8 Production in Human Cervical Epithelial Cell Cultures: The Role of Capsule Polysaccharide”. Clinical and Experimental Health Sciences 9/1 (March 2019), 49-52. https://doi.org/10.5152/clinexphealthsci.2018.1079.
JAMA Aksu B, Yanılmaz Ö. Group B Streptococci Induce Interleukin 8 Production in Human Cervical Epithelial Cell Cultures: The Role of Capsule Polysaccharide. Clinical and Experimental Health Sciences. 2019;9:49–52.
MLA Aksu, Burak and Özgür Yanılmaz. “Group B Streptococci Induce Interleukin 8 Production in Human Cervical Epithelial Cell Cultures: The Role of Capsule Polysaccharide”. Clinical and Experimental Health Sciences, vol. 9, no. 1, 2019, pp. 49-52, doi:10.5152/clinexphealthsci.2018.1079.
Vancouver Aksu B, Yanılmaz Ö. Group B Streptococci Induce Interleukin 8 Production in Human Cervical Epithelial Cell Cultures: The Role of Capsule Polysaccharide. Clinical and Experimental Health Sciences. 2019;9(1):49-52.

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