TY - JOUR
T1 - Host–parasite interaction associated with major mental illness
AU - Kano, Shin ichi
AU - Hodgkinson, Colin A.
AU - Jones-Brando, Lorraine
AU - Eastwood, Sharon
AU - Ishizuka, Koko
AU - Niwa, Minae
AU - Choi, Eric Y.
AU - Chang, Daniel J.
AU - Chen, Yian
AU - Velivela, Swetha D.
AU - Leister, Flora
AU - Wood, Joel
AU - Chowdari, Kodavali
AU - Ducci, Francesca
AU - Caycedo, Daniel A.
AU - Heinz, Elizabeth
AU - Newman, Emily R.
AU - Cascella, Nicola
AU - Mortensen, Preben B.
AU - Zandi, Peter P.
AU - Dickerson, Faith
AU - Nimgaonkar, Vishwajit
AU - Goldman, David
AU - Harrison, Paul J.
AU - Yolken, Robert H.
AU - Sawa, Akira
N1 - Publisher Copyright:
© 2018, Springer Nature Limited.
PY - 2020/1/1
Y1 - 2020/1/1
N2 - 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-Toxoplasma gondii (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 host immune responses against 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.
AB - 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-Toxoplasma gondii (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 host immune responses against 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.
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U2 - 10.1038/s41380-018-0217-z
DO - 10.1038/s41380-018-0217-z
M3 - Article
C2 - 30127472
AN - SCOPUS:85052563490
SN - 1359-4184
VL - 25
SP - 194
EP - 205
JO - Molecular psychiatry
JF - Molecular psychiatry
IS - 1
ER -