Abstract

Mature male mice produce a particularly high concentration of major urinary proteins (MUPs) in their scent marks that provide identity and status information to conspecifics. Darcin (MUP20) is inherently attractive to females and, by inducing rapid associative learning, leads to specific attraction to the individual male’s odour and location. Other polymorphic central MUPs, produced at much higher abundance, bind volatile ligands that are slowly released from a male’s scent marks, forming the male’s individual odour that females learn. Here, we show that infection of C57BL/6 males with LCMV WE variants (v2.2 or v54) alters MUP expression according to a male’s infection status and ability to clear the virus. MUP output is substantially reduced during acute adult infection with LCMV WE v2.2 and when males are persistently infected with LCMV WE v2.2 or v54. Infection differentially alters expression of darcin and, particularly, suppresses expression of a male’s central MUP signature. However, following clearance of acute v2.2 infection through a robust virus-specific CD8 cytotoxic T cell response that leads to immunity to the virus, males regain their normal mature male MUP pattern and exhibit enhanced MUP output by 30 days post-infection relative to uninfected controls. We discuss the likely impact of these changes in male MUP signals on female attraction and mate selection. As LCMV infection during pregnancy can substantially reduce embryo survival and lead to lifelong infection in surviving offspring, we speculate that females use LCMV-induced changes in MUP expression both to avoid direct infection from a male and to select mates able to develop immunity to local variants that will be inherited by their offspring.

Highlights

  • Introduction published maps and institutional affilMouse urine exhibits an obligate proteinuria, in the form of major urinary proteins (MUPs) [1,2,3,4]

  • We show that lymphocytic choriomeningitis virus (LCMV) WE v2.2 infection has differential effects on darcin, male-specific central MUPs and MUP10, which is expressed in both sexes

  • Many of the MUPs have unique masses that are revealed by high resolution electrospray ionization mass spectrometry (ESI-MS) of intact MUPs in desalted urine samples

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Summary

Introduction

Mouse urine exhibits an obligate proteinuria, in the form of major urinary proteins (MUPs) [1,2,3,4]. These proteins, which account for over 99% of the urinary protein in a healthy male mouse, are synthesized in the liver and enter the urine via the glomerulus. Mouse MUPs form two subclasses: a cluster of “central” MUPs that exhibit a very high degree of sequence similarity and a smaller group of “peripheral” MUPs that each exhibit greater sequence divergence and are encoded by genes that flank the central MUP region. MUPs bind small volatile organic compounds (VOCs) in a central cavity iations

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