Zika virus can make thousands of copies of itself in foetuses’ brains and in the placentas of pregnant women, which may help explain how the virus causes devastating birth defects and pregnancy losses even if a woman had only a minor illness. A new study by the United States Centers for Disease Control and Prevention (CDC) is the first to show Zika virus RNA replicating in brain tissues of infants with microcephaly who later died and in placentas of women who suffered pregnancy losses.
CDC scientists found Zika virus RNA persisted in foetal brains and in placentas for more than seven months after the mothers contracted Zika. The researchers also found evidence of the virus replicating in an infant with microcephaly who died two months after birth. The RNA levels were about 1,000 times higher in the infants’ brains than in the women’s placentas, according to the study published 13 December 2016 in CDC’s Emerging Infectious Diseases journal.
“Our findings show that Zika virus can continue to replicate in infants’ brains even after birth, and that the virus can persist in placentas for months – much longer than we expected,” said Julu Bhatnagar, PhD, lead of the molecular pathology team at CDC’s Infectious Diseases Pathology Branch and the study’s lead author. “We don’t know how long the virus can persist, but its persistence could have implications for babies born with microcephaly and for apparently healthy infants whose mothers had Zika during their pregnancies. More studies are needed to fully understand how the virus can affect babies.”
The study sheds light on how the virus can cross the placenta and infect the foetus’s brain. The researchers found Zika virus infects and proliferates in Hofbauer cells, a type of migratory immune cell in the placenta. Because the Hofbauer cells can move freely throughout the placenta, they may help transfer the virus to the foetus’s brain. Once there, the virus can infect various types of brain cells.
The researchers tested tissues from 52 patients with suspected Zika virus infection, including brain tissues (tested postmortem) from eight infants who had microcephaly and later died. They also tested placental tissues from 44 women: 22 who had adverse pregnancy or birth outcomes (miscarriage, elective termination, stillbirth or babies born with microcephaly) and 22 who had babies who appeared healthy. Most of the women were US residents who had travelled to countries with Zika outbreaks during their pregnancies. The eight infants with microcephaly who died were from Brazil and Colombia.
Zika most dangerous in early
As part of the Zika response, CDC’s Infectious Disease Pathology Branch developed a variety of tests to detect Zika virus in human tissue samples. The molecular tests used in this study can show evidence of Zika virus in tissues long after the virus would be undetectable by blood tests, which typically can only be used during the 12 weeks following infection.
“Our molecular tests for tissues extend the timeframe to detect Zika virus,” Bhatnagar said. “For women who contracted Zika virus during early pregnancy but were never diagnosed, these tests could help determine whether Zika virus may have caused their miscarriage, pregnancy loss, or adverse birth outcome.”
CDC recommends monitoring babies born to mothers who
had Zika virus infection during their pregnancy. CDC established the US
Zika Pregnancy Registry (USZPR) to monitor the effects of Zika virus infection
during pregnancy on foetal and infant outcomes. The data collected through
the USZPR is used to update recommendations
As of 12 December 2016, Zika virus outbreaks have been reported in 50 countries and territories, according to the CDC.
|Date of upload: 17th Janv 2017|
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