alexa Interleukin-6 and Interleukin-8 Secretions by Polarized
ISSN: 2155-9597

Journal of Bacteriology & Parasitology
Open Access

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Research Article

Interleukin-6 and Interleukin-8 Secretions by Polarized Airway Epithelial Cells Infected by Normal and Small-Colony Variant Staphylococcus aureus Strains are Similar Despite Differences in Infection Levels

Gabriel Mitchell, Myriame Lafrance, Brian G. Talbot and François Malouin*

Centre d’Étude et de Valorisation de la Diversité Microbienne (CEVDM), Département de Biologie, Faculté des Sciences, Université de Sherbrooke, QC, Canada, J1K 2R1

*Corresponding Author:
Dr. François Malouin
Département de Biologie
Faculté des Sciences, Université de Sherbrooke
2500 Boul. Université, Sherbrooke, QC
Canada, J1K 2R1
Tel: (819) 821-8000, (61202)
Fax: (819) 821-8049
E-mail: [email protected]

Received date: August 08, 2011; Accepted date: October 10, 2011; Published date: October 28, 2011

Citation: Mitchell G, lafrance M, Talbot BG, Malouin F (2011) Interleukin-6 and Interleukin-8 Secretions by Polarized Airway Epithelial Cells Infected by Normal and Small-Colony Variant Staphylococcus aureus Strains are Similar Despite Differences in Infection Levels. J Bacteriol Parasitol 2:122. doi: 10.4172/2155- 9597.1000122

Copyright: © 2011 Mitchell G, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

 

Abstract

Staphylococcus aureus small-colony variants (SCVs) can efficiently infect non-professional phagocytes and are often referred to as facultative intracellular pathogens. The ability to hide and persist within host cells is likely to contribute to the development of chronic S. aureus infections such as those observed in the lungs of cystic fibrosis patients. Polarized human pulmonary Calu-3 cells were used to confirm that S. aureus small-colony variants (SCVs) persist within epithelial cells without exacerbating the innate immune response. Whereas all studied S. aureus strains significantly induced the secretion of Interleukin-6 (IL-6) and Interleukin-8 (IL-8) by Calu-3 cells 48 hours after cellular invasion, dead bacteria did not. Surprisingly, no difference in the secretion of these interleukins was detected between cells infected with normal and SCV strains despite the marked difference in infection levels. This study supports the hypothesis that despite their increased ability to persist inside epithelial cells, SCVs do not over activate the host immune response in comparison to normal strains. SCVs may thus help to perpetuate infection without exacerbation of the host immune response.

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