The severity of infection from Toxoplasma gondii could depend on the damage suffered by the nerve cells, according to a new Johns Hopkins study.
Past research suggests that the cat-borne parasite, estimated to infect 25 percent of people worldwide, can trigger or exacerbate psychotic symptoms and schizophrenia in genetically predisposed people.
The findings of the new study, published in the March issue of the journal Infection and Immunity, help explain why the infection causes serious disease in some but not in others and clarify its role in psychiatric disorders, the researchers say.
"We already know that toxoplasmosis can play a role in some psychiatric disorders, but up until now we didn't know why. Working with human nerve cells, our study shows the exact alterations triggered by each strain that can eventually manifest themselves as symptoms," says senior investigator Robert Yolken, M.D., a neurovirologist at Johns Hopkins Children's Center.
The researchers injected human nerve cells with the three most common toxoplasma strains, each of which caused a different pattern of gene expression. One of the most basic functions in all living organisms, gene expression occurs when a gene is switched on to release a substance that tells cells what to do or not do, determining the cells' biologic behavior. Gene expression can be turned on and off, stepped up or down by various factors, including viral and bacterial invasions.
Cells infected with toxoplasma type I the most virulent strain in mice had the greatest impact on gene expression, altering more than 1,000 genes, 28 of them linked to brain development and central nervous system function and 31 others to nerve impulse and signaling.
Cells injected with the less virulent types II and III had low and moderate levels of gene expression. Infection with toxoplasma type II affected 78 genes, some of which were related to growth, certain hormones and circadian rhythm, while type III altered 344 genes, some of which were linked to metabolism.
A handful of genes were affected by all three strains, notably a gene called VIPR2 that regulates neurotransmitters and nerve signaling and may play a role in schizophrenia, the researchers say.
The findings must now be confirmed in clinical studies with people. "While disease course in humans is often more unpredictable than what we see in the controlled setting of a lab, these results give us a fascinating first look into the distinct genetic cascade of reactions that each strain can unlock and may one day serve as the basis for individualized treatment of symptomatic infections," says lead investigator Jianchun Xiao, Ph.D., a neurovirologist at the Stanley Division of Developmental Neurovirology at Hopkins.
A 2008 study by Yolken and colleagues revealed that toxoplasma infection increases the risk for schizophrenia and could precipitate the disease in genetically predisposed people, a classic example of how genes and environment come together in the development of disease.
Most infections with toxoplasma occur early in life following exposure to the parasite from cat feces or undercooked beef or pork. Farm animals and rodents also get infected, but the parasite reaches full sexual reproduction only in cats. Infections rarely cause symptoms, but the parasite remains in the body and can reactivate after lying dormant for years.
Co-investigators on the study included Lorraine Jones-Brando, M.D., and C. Conover Talbot Jr., both of Hopkins. The research was funded by the Stanley Medical Research Institute.