Streptococcus pneumoniae induces expression of the antibacterial CXC chemokine MIG/CXCL9 via MyD88-dependent signaling in a murine model of airway infection.
(2010) In Microbes and Infection 12. p.565-573- Abstract
- MIG/CXCL9 belongs to the CXC family of chemokines and participates in the regulation of leukocyte-trafficking and angiogenesis. Certain chemokines, including human MIG/CXCL9, exert strong antibacterial activity in vitro, although the importance of this property in vivo is unknown. In the present study, we investigated the expression and a possible role for MIG/CXCL9 in host defense during mucosal airway infection caused by Streptococcus pneumoniae in vivo. We found that intranasal challenge of C57BL/6 wild-type mice with pneumococci elicited production of high levels of MIG/CXCL9 in the lungs via the MyD88-dependent signaling pathway. Whereas both human and murine MIG/CXCL9 showed efficient killing of S. pneumoniae in vitro, MIG/CXCL9... (More)
- MIG/CXCL9 belongs to the CXC family of chemokines and participates in the regulation of leukocyte-trafficking and angiogenesis. Certain chemokines, including human MIG/CXCL9, exert strong antibacterial activity in vitro, although the importance of this property in vivo is unknown. In the present study, we investigated the expression and a possible role for MIG/CXCL9 in host defense during mucosal airway infection caused by Streptococcus pneumoniae in vivo. We found that intranasal challenge of C57BL/6 wild-type mice with pneumococci elicited production of high levels of MIG/CXCL9 in the lungs via the MyD88-dependent signaling pathway. Whereas both human and murine MIG/CXCL9 showed efficient killing of S. pneumoniae in vitro, MIG/CXCL9 knock-out mice were not more susceptible to pneumococcal infection. Our data demonstrate that, in vivo this chemokine probably has a redundant role, acting together with other antibacterial peptides and chemokines, in innate and adaptive host defense mechanisms against pneumococcal infections. (Less)
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/1595427
- author
- Eliasson, Mette LU ; Mörgelin, Matthias LU ; Farber, Joshua M ; Egesten, Arne LU and Albiger, Barbara LU
- organization
- publishing date
- 2010
- type
- Contribution to journal
- publication status
- published
- subject
- in
- Microbes and Infection
- volume
- 12
- pages
- 565 - 573
- publisher
- Elsevier
- external identifiers
-
- wos:000279561500008
- pmid:20381636
- scopus:77953011315
- pmid:20381636
- ISSN
- 1769-714X
- DOI
- 10.1016/j.micinf.2010.03.014
- language
- English
- LU publication?
- yes
- id
- 33c05dde-30f7-49c8-8473-dfda83de4972 (old id 1595427)
- alternative location
- http://www.ncbi.nlm.nih.gov/pubmed/20381636?dopt=Abstract
- date added to LUP
- 2016-04-04 07:22:04
- date last changed
- 2022-04-23 08:07:50
@article{33c05dde-30f7-49c8-8473-dfda83de4972, abstract = {{MIG/CXCL9 belongs to the CXC family of chemokines and participates in the regulation of leukocyte-trafficking and angiogenesis. Certain chemokines, including human MIG/CXCL9, exert strong antibacterial activity in vitro, although the importance of this property in vivo is unknown. In the present study, we investigated the expression and a possible role for MIG/CXCL9 in host defense during mucosal airway infection caused by Streptococcus pneumoniae in vivo. We found that intranasal challenge of C57BL/6 wild-type mice with pneumococci elicited production of high levels of MIG/CXCL9 in the lungs via the MyD88-dependent signaling pathway. Whereas both human and murine MIG/CXCL9 showed efficient killing of S. pneumoniae in vitro, MIG/CXCL9 knock-out mice were not more susceptible to pneumococcal infection. Our data demonstrate that, in vivo this chemokine probably has a redundant role, acting together with other antibacterial peptides and chemokines, in innate and adaptive host defense mechanisms against pneumococcal infections.}}, author = {{Eliasson, Mette and Mörgelin, Matthias and Farber, Joshua M and Egesten, Arne and Albiger, Barbara}}, issn = {{1769-714X}}, language = {{eng}}, pages = {{565--573}}, publisher = {{Elsevier}}, series = {{Microbes and Infection}}, title = {{Streptococcus pneumoniae induces expression of the antibacterial CXC chemokine MIG/CXCL9 via MyD88-dependent signaling in a murine model of airway infection.}}, url = {{https://lup.lub.lu.se/search/files/7451589/5135877.pdf}}, doi = {{10.1016/j.micinf.2010.03.014}}, volume = {{12}}, year = {{2010}}, }