E very year, an estimated 96 million persons worldwide are given a clinical diagnosis of severe dengue infection (1). In 2017, a total of 188,401 cases of dengue were diagnosed in India, and the mortality rate was 0.1%. The mortality rate in Maharashtra State was 0.8% in 2017, nearly 8 times higher than the national average (2,3). The prevalence of dengue infection among pregnant women is not reported, but pregnant women may be uniquely susceptible to dengue infection because of the immune changes that occur during pregnancy (4). In some countries in Southeast Asia, dengue fever is the most common cause of acute febrile illness during pregnancy (5). Dengue infection during pregnancy has been associated with poor maternal and infant outcomes, including preterm birth (6), hemorrhage, preeclampsia, and caesarean delivery (7-15). Dengue virus can also be vertically transmitted to the infant, resulting in neonatal dengue, thrombocytopenia, and cerebral hemorrhage (16-19). Vertical transmission is most likely if the infection occurs in the third trimester or is present during delivery by cesarean section (20). Despite the devastating consequences, the diagnosis of dengue infection during pregnancy remains challenging. This challenge is partially caused by overlapping signs and symptoms of dengue infection with other conditions, such as HELLP (hemolysis, elevated liver enzymes, low platelet count) syndrome, pneumonia, pulmonary embolism, and other febrile illnesses (21,22). Moreover, molecular assays to diagnose dengue are not widely available. However, there is a remarkable reduction in the case-fatality rate after early diagnosis and access to appropriate medical care (23). This study was planned after detection of Zika virus in India. The goal of this study was to determine the prevalence of dengue, chikungunya, and Zika virus among pregnant women in Pune, India. We also aimed to identify clinical predictors of these infections to improve screening and detection during the antenatal setting. Methods Ethics This study was approved by the Byramjee Jeejeebhoy Medical College Clinical Trials Unit and Johns