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Host-parasite interaction associated with major mental illness

Clinical studies frequently report that patients with major mental illness such as schizophrenia and bipolar disorder have co-morbid physical conditions, suggesting that systemic alterations affecting both brain and peripheral tissues might underlie the disorders. Numerous studies have reported elev...

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Detalles Bibliográficos
Autores principales: Kano, Shin-ichi, Hodgkinson, Colin A., Jones-Brando, Lorraine, Eastwood, Sharon, Ishizuka, Koko, Niwa, Minae, Choi, Eric Y., Chang, Daniel J., Chen, Yian, Velivela, Swetha D., Leister, Flora, Wood, Joel, Chowdari, Kodavali, Ducci, Francesca, Caycedo, Daniel A, Heinz, Elizabeth, Newman, Emily R., Cascella, Nicola, Mortensen, Preben B., Zandi, Peter P., Dickerson, Faith, Nimgaonkar, Vishwajit, Goldman, David, Harrison, Paul J., Yolken, Robert, Sawa, Akira
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6382596/
https://www.ncbi.nlm.nih.gov/pubmed/30127472
http://dx.doi.org/10.1038/s41380-018-0217-z
Descripción
Sumario:Clinical studies frequently report that patients with major mental illness such as schizophrenia and bipolar disorder have co-morbid physical conditions, suggesting that systemic alterations affecting both brain and peripheral tissues might underlie the disorders. Numerous studies have reported elevated levels of anti-T. gondii antibodies in patients with major mental illnesses, but the underlying mechanism was unclear. Using multidisciplinary epidemiological, cell biological, and gene expression profiling approaches, we report here multiple lines of evidence suggesting that a major mental illness-related susceptibility factor, Disrupted in schizophrenia (DISC1), is involved in altered host immune responses against Toxoplasma gondii (T. gondii) infection. Specifically, our cell biology and gene expression studies have revealed that DISC1 Leu607Phe variation, which changes DISC1 interaction with activating transcription factor 4 (ATF4), modifies gene expression patterns upon T. gondii infection. Our epidemiological data have also shown that DISC1 607 Phe/Phe genotype was associated with higher T. gondii antibody levels in sera. Although further studies are required, our study provides mechanistic insight into one of the few well-replicated serological observations in major mental illness.