Gamma-irradiation-killed Streptococcus pneumoniae potently induces the expression of IL-6 and IL-8 in human bronchial epithelial cells. (November 2018)

• Record Type: Journal Article
• Authors: Jwa, Min Yong; Ko, Eun Byeol; Kim, Hyun Young; Kim, Sun Kyung; Jeong, Soyoung; Seo, Ho Seong; Yun, Cheol-Heui; Han, Seung Hyun
• Is Part Of: Microbial pathogenesis. Volume 124(2018)
• Page Start: 38
• Page End: 46
• Publication Date: 2018-11
• Subjects: Streptococcus pneumoniae -- Gamma-irradiation -- BEAS-2B -- Vaccine -- Innate immunity; Pathogenic microorganisms -- Periodicals; Pathology, Molecular -- Periodicals; Communicable Diseases -- microbiology -- Periodicals; Communicable Diseases -- parasitology -- Periodicals; Micro-organismes pathogènes -- Périodiques; Pathologie moléculaire -- Périodiques; Electronic journals; 616.9041
• DOI: 10.1016/j.micpath.2018.08.015
• Languages: English
• ISSNs: 0882-4010

Abstract

Abstract: Streptococcus pneumoniae is a major respiratory pathogen that can cause pneumonia, meningitis, and otitis media. Although capsular polysaccharide-based vaccines are commercially available, there is a need for broad-spectrum, serotype-independent, and cost-effective vaccines. Recently, an intranasal vaccine formulated with gamma-irradiated nonencapsulated S. pneumoniae whole cells has been developed and its immunogenicity is under investigation. Since innate immunity influences the subsequent adaptive immunity, in the present study, we investigated the immunostimulatory activity of gamma-irradiated S. pneumoniae (r-SP) in the human bronchial epithelial cell-line, BEAS-2B, by comparing with heat-inactivated S. pneumoniae (h-SP) and formalin-inactivated S. pneumoniae (f-SP). r-SP potently induced interleukin (IL)-6 and IL-8 at both mRNA and protein levels in a dose- and time-dependent manner, whereas h-SP and f-SP poorly induced them. Of note, the mRNA levels of IL-6 and IL-8 were approximately two-fold higher when cells were stimulated with 3 × 10 7 CFU/ml of r-SP for 3 h, while the protein levels of IL-6 and IL-8 were approximately five-fold higher after stimulation with 3 × 10 7 CFU/ml of r-SP for 24 h. Furthermore, r-SP exhibited potent activation of Toll-like receptor 2 compared with h-SP or f-SP. The expression of IL-6 and IL-8 induced by r-SP was mediated through the activation of mitogen-activated protein kinases. Remarkably, when r-SP was further treated with heat or formalin, there was a decrease in the aforementioned activities. Taken together, we suggest that r-SP stimulates the human respiratory epithelial cells to produce the cytokines IL-6 and IL-8, which might influence the induction of adaptive immune responses. Highlights: r-SP induces IL-6 and IL-8 expression more potently than h-SP or f-SP in BEAS-2B cells. r-SP phosphorylates MAP kinases more potently than h-SP or f-SP in BEAS-2B cells. r-SP strongly activates TLR2 compared with h-SP or f-SP. Soluble components of r-SP are responsible for the potent immunostimulatory activity.