De Novo Generation and Characterization of New Zika Virus Isolate Using Sequence Data from a Microcephaly Case

Author:

Setoh Yin Xiang1,Prow Natalie A.2,Peng Nias1,Hugo Leon E.3,Devine Gregor3,Hazlewood Jessamine E.2,Suhrbier Andreas2,Khromykh Alexander A.1ORCID

Affiliation:

1. Australian Infectious Diseases Research Centre, School of Chemistry and Molecular Biosciences, University of Queensland, St. Lucia, Queensland, Australia

2. Inflammation Biology Group, QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia

3. Mosquito Control Group, QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia

Abstract

The major complications of an ongoing Zika virus outbreak in the Americas and Asia are congenital defects caused by the virus’s ability to cross the placenta and infect the fetal brain. The ability to generate molecular tools to analyze viral isolates from the current outbreak is essential for furthering our understanding of how these viruses cause congenital defects. The majority of existing viral isolates and infectious cDNA clones generated from them have undergone various numbers of passages in cell culture and/or suckling mice, which is likely to result in the accumulation of adaptive mutations that may affect viral properties. The approach described herein allows rapid generation of new, fully functional Zika virus isolates directly from deep sequencing data from virus-infected tissues without the need for prior virus passaging and for the generation and propagation of full-length cDNA clones. The approach should be applicable to other medically important flaviviruses and perhaps other positive-strand RNA viruses.

Funder

Australian Infectious Diseases Research Centre, University of Queensland and QIMR Berghomer Medical Research Institutes

Publisher

American Society for Microbiology

Subject

Molecular Biology,Microbiology

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