Abstract | BACKGROUND: Neonates are at a higher risk for bacterial meningitis than children of other age groups. Although the mortality rates have decreased over the past few decades, neonatal meningitis is still a severe disease with high morbidity. For bacterial meningitis, antibiotic therapy is the primary choice for management. However, neurologic complications often cannot be averted; ∼40% of survivors exhibit neurological sequelae. Escherichia coli infection is the common cause of neonatal meningitis. Previously, we have demonstrated that the recombinant loop 1-3, loop 2-3, and loop 2-4 fragments of OmpA protein can protect mice from death after intracerebral E. coli infection. In this study, the protective effects of the recombinant OmpA protein fragments in E. coli intracerebral infections were investigated. METHODS: RESULTS: In this study, we demonstrated that the expression of interleukin-17 and other cytokines, chemokines, inducible nitric oxide synthase, and cyclooxygenase-2 are involved in the inflammatory processes of intracerebral E. coli infection. We also demonstrated that specific recombinant OmpA protein fragments (L1-3, L2-3, L2-4, and L3) can regulate cytokine, chemokine, nitric oxide synthase, and cyclooxygenase-2 expression and, subsequently, protect mice from death caused by intracerebral infection of E. coli. CONCLUSION: This finding indicates the potential for developing a new therapeutic approach to improve the prognosis of bacterial meningitis.
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Authors | Wen-Shyang Hsieh, Yi-Yuan Yang, Pei-Hsuan Lin, Chia-Chih Chang, Hsueh-Hsia Wu |
Journal | Journal of microbiology, immunology, and infection = Wei mian yu gan ran za zhi
(J Microbiol Immunol Infect)
Vol. 49
Issue 6
Pg. 843-850
(Dec 2016)
ISSN: 1995-9133 [Electronic] England |
PMID | 26190062
(Publication Type: Journal Article)
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Copyright | Copyright © 2015. Published by Elsevier B.V. |
Chemical References |
- Bacterial Outer Membrane Proteins
- Interleukin-17
- Peptide Fragments
- OMPA outer membrane proteins
- Nitric Oxide Synthase Type II
- Cyclooxygenase 2
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Topics |
- Animals
- Bacterial Outer Membrane Proteins
(genetics, immunology, pharmacology)
- Cell Line, Tumor
- Cyclooxygenase 2
(biosynthesis, immunology)
- Escherichia coli
(immunology)
- Humans
- Infant, Newborn
- Interleukin-17
(biosynthesis)
- Male
- Meningitis, Escherichia coli
(immunology, microbiology, prevention & control)
- Mice, Inbred C57BL
- Nitric Oxide Synthase Type II
(biosynthesis, immunology)
- Peptide Fragments
(immunology, pharmacology)
- Rats
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