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J Med Microbiol 55 (2006), 695-702; DOI: 10.1099/jmm.0.46496-0
© 2006 Society for General Microbiology
ISSN 1473-5644

Human herpesvirus-6 dysregulates monocyte-mediated anticryptococcal defences

Claudio Cermelli1, Valeria Cenacchi1, Francesca Beretti1, Francesco Pezzini1, Dario Di Luca2 and Elisabetta Blasi1

1 Department of Hygiene, Microbiology and Biostatistics, University of Modena and Reggio Emilia, Via Campi 287, I-41100 Modena, Italy

2 Department of Experimental and Diagnostic Medicine, University of Ferrara, Ferrara, Italy

Correspondence
Claudio Cermelli
c.cermelli{at}unimo.it

Received 3 January 2006
Accepted 17 February 2006


In order to investigate the interplay occurring between pathogens in the course of double infections, an in vitro model was set up in which the monocytic cell line THP-1 was exposed to Cryptococcus neoformans (Cn) and human herpesvirus 6 (HHV-6). Cn and HHV-6, both highly neurotropic, can cause serious diseases of the central nervous system and have monocytes, among other cell types, as target cells, causing alteration of their secretion pattern. Here, it was shown that unlike THP-1 cells exposed to cell-free virus inocula, THP-1 exposed to HHV-6-producing lymphocytes exhibited augmented phagocytosis against Cn. The phenomenon occurred after 24 h of monocyte/lymphocyte co-culture and was independent of direct cell-to-cell contact. Moreover, in the presence of HHV-6, THP-1 cells expressed enhanced secretory responses but reduced capability to counteract fungal infection: the enhanced ingestion by monocytes was followed by facilitated fungal survival and replication. These data provide initial in vitro evidence that HHV-6 may dysregulate monocyte-mediated anticryptococcal defences with an overall pro-cryptococcus result.


Abbreviations: Cn, Cryptococcus neoformans; CNS, central nervous system; CPE, cytopathic effect; HHV-6, human herpesvirus-6; IFA, immunofluorescence assay; IHC, immunohistochemistry.




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R. Micol, P. Buchy, J. Galimand, D. Veasna, L. Ferradini, S. Balkan, P. J. Guerin, P.-R. Martin, A. Fontanet, O. Lortholary, et al.
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