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  4. Analysis of Corynebacterium diphtheriae macrophage interaction
 
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2017
Journal Article
Title

Analysis of Corynebacterium diphtheriae macrophage interaction

Title Supplement
Dispensability of corynomycolic acids for inhibition of phagolysosome maturation and identification of a new gene involved in synthesis of the corynomycolic acid layer
Abstract
Corynebacterium diphtheriae is the causative agent of diphtheria, a toxin mediated disease of upper respiratory tract, which can be fatal. As a member of the CMNR group, C. diphtheriae is closely related to members of the genera Mycobacterium, Nocardia and Rhodococcus. Almost all members of these genera comprise an outer membrane layer of mycolic acids, which is assumed to influence host-pathogen interactions. In this study, three different C. diphtheriae strains were investigated in respect to their interaction with phagocytic murine and human cells and the invertebrate infection model Caenorhabditis elegans. Our results indicate that C. diphtheriae is able to delay phagolysosome maturation after internalization in murine and human cell lines. This effect is independent of the presence of mycolic acids, as one of the strains lacked corynomycolates. In addition, analyses of NF-kBinduction revealed a mycolate- independent mechanism and hint to detrimental effects of the different strains tested on the phagocytic cells. Bioinformatics analyses carried out to elucidate the reason for the lack of mycolates in one of the strains led to the identification of a new gene involved in mycomembrane formation in C. diphtheriae.
Author(s)
Ott, L.
Hacker, E.
Kunert, T.
Karrington, I.
Etschel, P.
Lang, R.
Wiesmann, V.
Wittenberg, T.
Singh, A.
Varela, C.
Bhatt, A.
Sangal, V.
Burkovski, A.
Journal
PLoS one. Online journal  
Project(s)
SFB 796 "Steuerungsmechanismen mikrobieller Effektoren in Wirtszellen"
Funder
Deutsche Forschungsgemeinschaft DFG  
Open Access
Link
Link
DOI
10.1371/journal.pone.0180105
Additional link
Full text
Language
English
Fraunhofer-Institut für Integrierte Schaltungen IIS  
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