" An in vivo imaging approach is particularly advantageous to study progression of ZIKV-induced neurological sequelae because the development of neuropathology and congenital defects is a dynamic process. "First draft submitted: 9 November 2017; Accepted for publication: 21 November 2017; Published online: 10 January 2018Zika virus (ZIKV) is a mosquito-borne flavivirus that has emerged since 2007 causing human outbreaks in Africa, Asia, Oceania and most recently in the Americas. Mortality is not a common feature of human ZIKV infection, which is generally asymptomatic and self-limiting in most individuals. However, during the recent epidemics in Asia and the Americas, more severe clinical complications have been reported. Severe disease is characterized by neurological complications, which in adults include Guillain-Barré syndrome or in a few cases, encephalopathy, meningoencephalitis and acute myelitis [1]. ZIKV infection in pregnant women is a major global public health concern due to its link to congenital abnormalities including microcephaly, spontaneous abortion and intrauterine growth restriction [2], now referred to as congenital Zika syndrome.The unexpectedly frequent and severe clinical complications of ZIKV infection have prompted intense research on host-virus interactions, which remains a high priority research area. It is crucial that we characterize the neuropathogenesis and causative roles of ZIKV infection in the etiology of fetal microcephaly and other congenital malformations during pregnancy. Appropriate use of animal models is needed to address some of these key unanswered questions regarding the pathogenesis of ZIKV and to evaluate candidate medical countermeasures. Current approaches to study viral pathogenesis involve reduced mortality or extended time-to-death as the efficacy end point, viremia as an index of infection and serial necropsies to establish the pathological consequences of infection. New technology in the form of molecular imaging tools shifts the classical paradigm of serial necropsies and offers less invasive alternatives capable of providing a dynamic assessment of pathogen infection in real time. An in vivo imaging approach is particularly advantageous to study progression of ZIKV-induced neurological sequelae because the development of neuropathology and congenital defects is a dynamic process. While molecular imaging has been used to characterize disease progression and evaluate drugs in the areas of neuroscience, cardiovascular, inflammation and oncology, application of imaging in infectious disease is limited [3].We recently described the ability and sensitivity of PET imaging using [ 18 F]DPA-714, a translocator protein (TSPO) 18 kDa radioligand, to detect and quantify neuroinflammation in ZIKV-infected mice [4]. Our results demonstrated that global neuroinflammation plays an important role in the progression of ZIKV infection in a transiently immunosuppressed mouse model [5]. Importantly, the use of [18 F]DPA-714 PET imaging was more sensitive compared with standard...