Recombinant OmpA protein fragments mediate interleukin-17 regulation to prevent Escherichia coli meningitis

Autor: Chia Chih Chang, Hsueh Hsia Wu, Pei Hsuan Lin, Wen Shyang Hsieh, Yi Yuan Yang
Rok vydání: 2016
Předmět:
Male
0301 basic medicine
Microbiology (medical)
Chemokine
Meningitis
Escherichia coli

medicine.medical_treatment
Nitric Oxide Synthase Type II
medicine.disease_cause
Neonatal meningitis
Microbiology
law.invention
03 medical and health sciences
0302 clinical medicine
law
Immunology and Microbiology(all)
Cell Line
Tumor

Escherichia coli
medicine
Animals
Humans
Immunology and Allergy
Escherichia coli infection
General Immunology and Microbiology
biology
Interleukin-17
Infant
Newborn

General Medicine
medicine.disease
Virology
outer membrane protein A
Peptide Fragments
Rats
NOS-2
Mice
Inbred C57BL

Nitric oxide synthase
IL-17
030104 developmental biology
Infectious Diseases
Cytokine
Cyclooxygenase 2
biology.protein
Recombinant DNA
Interleukin 17
bacterial meningitis
030217 neurology & neurosurgery
Bacterial Outer Membrane Proteins
Zdroj: Journal of Microbiology, Immunology and Infection. 49:843-850
ISSN: 1684-1182
DOI: 10.1016/j.jmii.2015.05.019
Popis: 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 The effects of E. coli intracerebral infection on cytokine and chemokine expression were determined. We also used various recombinant fragments of the OmpA protein to investigate the effects of these recombinant OmpA protein fragments on cytokine and chemokine expression. 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.
Databáze: OpenAIRE