Prolonged Detection of Zika Virus in Vaginal Secretions and Whole Blood

Kristy O. Murray; Rodion Gorchakov; Anna R. Carlson; Rebecca Berry; Lilin Lai; Muktha Natrajan; Melissa N. Garcia; Armando Correa; Shital M. Patel; Kjersti Aagaard; Mark J. Mulligan

Disclosures

Emerging Infectious Diseases. 2016;23(1) 

In This Article

Conclusions

Given recent concerns regarding the ongoing epidemic of Zika virus disease, there is an urgent need to document the natural history of infection and assess transmission risk through nonvector routes. We had the unique opportunity to prospectively monitor the clinical and virologic course of Zika virus infection in a patient starting on day 0.

We detected viral shedding in vaginal secretions up to day 14. Only 1 human study reported Zika virus RNA in cervical mucous up to day 11 after onset of signs and symptoms.[10] These findings are supported by recent results for 2 animal models. Zika virus (Asian lineage strain) RNA was detected in vaginal swab specimens obtained on days 1 and 7 postinfection of nonpregnant female rhesus macaques.[11] Zika virus replication was also detected in vaginal mucosa of mice.[12]

We could not determine whether positive results by qRT-PCR indicated replicating virus. With the recent finding of possible female-to-male virus transmission,[5] infectious virus might be present in the vaginal canal and could serve as a risk for sexual or intrapartum transmission.

We detected viral RNA in serum up to 8 days and in whole blood up to 81 days after onset of illness. Diagnosis of infection currently relies mostly on PCR detection of Zika virus in serum. With concerns for Zika virus infection during pregnancy, screening of whole blood might be more sensitive in identifying infected patients, particularly if an asymptomatic patient has traveled from an area where exposure is a concern, had high-risk sexual contact, or is convalescing and PCR for a serum sample would probably yield a negative result.

Our observation is further supported by another recent study that found whole blood samples positive for Zika virus by PCR up to 2 months postinfection.[13] In our study, we confirmed that a positive result was attributed to the erythrocyte component of whole blood, similar to what has been found in studies of West Nile virus.[14,15] One study found that West Nile virus adheres to erythrocytes and could infect Vero cells.[14] Although we did not observe infectious virus associated with erythrocyte positivity for Zika virus at day 64, this finding is still of concern and requires further investigation. Because the last whole blood sample collected on day 81 was positive for Zika virus RNA, follow-up testing will continue to define the longevity of viremia in whole blood.

In conclusion, this case study advances understanding of the natural history of Zika virus. It provides new findings, including detection of Zika virus RNA in vaginal secretions up to day 14 and in erythrocytes up to day 81, the longest reported duration of detection in this sample type. A desquamating rash developed on the hands and feet of the patient, which we presume was related to her infection. To our knowledge, this finding has not been previously described.

Additional studies involving larger cohorts of acutely ill Zika virus–infected patients tested over a longer period would solidify our understanding of the natural history of infection, duration of viral detection, and clinical outcomes. These studies will enable further development of evidence-based policies regarding diagnosis and clinical management of Zika virus–infected patients.

Dr. Murray is Associate Vice-Chair for Research and Associate Professor of Pediatric Tropical Medicine in the Department of Pediatrics, Baylor College of Medicine and Texas Children’s Hospital, Houston, TX, and serves as Assistant Dean of the National School of Tropical Medicine. Her research interests are vectorborne and zoonotic diseases.

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