Abstract

We used paired-end Illumina deep sequencing and de novo assembly to determine the genome sequence of herpes simplex virus 1 (HSV-1) strain MacIntyre (aka McIntyre). The MacIntyre strain originated from the brain of a patient with lethal HSV encephalitis and has a unique limitation in its neuronal spread, moving solely in the retrograde direction.

Highlights

  • We used Illumina deep sequencing and de novo assembly to determine the genome sequence of herpes simplex virus 1 (HSV-1) strain MacIntyre

  • The MacIntyre strain originated from the brain of a patient with lethal HSV encephalitis [1]

  • As in prior studies [17, 24,25,26,27,28,29], we found that a majority of HSV MacIntyre proteins have coding variations compared to those of the HSV-1 reference strain 17

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Summary

Introduction

We used Illumina deep sequencing and de novo assembly to determine the genome sequence of herpes simplex virus 1 (HSV-1) strain MacIntyre ( spelled MacIntyre B, McIntyre, and McIntyre B). The MacIntyre strain originated from the brain of a patient with lethal HSV encephalitis [1]. MacIntyre was passaged through multiple cell types and species [1, 2]. Later studies revealed a severe defect in the anterograde spread of HSV-1 MacIntyre in the central nervous systems in rat, mouse, and primate models [4,5,6,7,8,9,10,11,12].

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