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Epidemiological and immun… - Göteborgs universitet Till startsida
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Epidemiological and immunological studies of environmental mycobacteria - with focus on Mycobacterium abscessus

Författare Bodil Jönsson
Datum för examination 2009-03-19
ISBN 978-91-628-7708-8
Publiceringsår 2009
Publicerad vid Institutionen för biomedicin, avdelningen för infektionssjukdomar
Språk en
Länkar hdl.handle.net/2077/19060
Ämnesord Bacteriology, Immunology, Epidemiology, Mycobacteria, Mycobacterium abscessus, Colony morphology, Mycobacterial lipids, Cystic fibrosis, PFGE, Human PBMC, Cytokine, Phagocytosis
Ämneskategorier Medicin och Hälsovetenskap


Mycobacterium avium, M. abscessus and M. gordonae are three mycobacterial species that are ubiquitous in the environment. M. gordonae is non-pathogenic, while M. avium and M. abscessus can cause skin abscesses and airway disease, the latter mainly in patients with cystic fibrosis. The aim of this thesis was to examine the molecular epidemiology of M. abscessus and interactions of environmental mycobacteria with the human immune system. M. abscessus isolates from the airways of cystic fibrosis patients and from skin infections in patients injured during the tsunami catastrophe in Thailand 2004 were analysed by pulsed-field gel electrophoresis (PFGE). Almost all patients had unique strains, indicating that patient-to-patient transmission was rare. M. abscessus exhibits two colony variants; smooth and rough, the latter thought to be more virulent. Rough isolates dominated in chronic airway infection, while smooth strains caused wound infection or were transient colonizers of the airways, without associated symptoms. Environmental mycobacteria induced a unique cytokine pattern in human peripheral blood mononuclear cells (PBMC) characterized by very high levels of IL-17, high levels of IL-10, moderate levels of IL-23, relatively little IFN-, and no IL-12. The cytokine pattern induced by M. abscessus, M. avium and M. gordonae was identical, despite differences in pathogenic potential. Mycobacterial surface lipids and lipoarabinomannans induced very large amounts of IL-17, but down-regulated production of Th1 cytokines. Morphological analysis of PBMC interacting with M. abscessus showed that smooth isolates were readily phagocytosed, while rough strains formed multibacterial cords that escaped phagocytosis. Instead, monocytes appeared to entrap cord-forming bacteria in meshworks containing dsDNA and histones. These meshworks resembled NETs previously described in neutrophils, but to our knowledge, extracellular traps formed by monocytes have not previously been described. Rough isolates of M. abscessus induced significantly less IL-10 and IL-23, but more IL-1 than smooth isolates. Our results suggest that cord formation increases mycobacterial virulence and that mycobacterial cell wall lipids efficiently modulate innate responses and possess unique IL-17 inducing properties. The cellular basis for this IL-17 production remains to be determined.

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