Sialic acid and PirB are not required for targeting of neural circuits by neurotropic mammalian orthoreovirus

• Published in: mSphere 2024-10, Vol.9 (10), p.e0062924
• Main Authors: Griswold, Kira A, Vasylieva, Iaroslavna, Smith, Megan C, Fiske, Kay L, Welsh, Olivia L, Roth, Alexa N, Watson, Alan M, Watkins, Simon C, Sutherland, Danica M, Dermody, Terence S
• Format: Article
• Language: English
• Subjects: Animals; Animals, Newborn; Brain - virology; CLARITY; Female; Male; Mammalian orthoreovirus 3 - genetics; Mammalian orthoreovirus 3 - physiology; Mice; Mice, Inbred C57BL; MiPACT-HCR; N-Acetylneuraminic Acid - metabolism; Neurons - virology; neuropathogenesis; neurotropic viruses; Orthoreovirus, Mammalian - genetics; Orthoreovirus, Mammalian - physiology; PirB; Receptors, Immunologic - genetics; Receptors, Immunologic - metabolism; Receptors, Virus - genetics; Receptors, Virus - metabolism; Reoviridae Infections - virology; reovirus; Research Article; Viral Tropism; Virology
• ISSN: 2379-5042; 2379-5042
• DOI: 10.1128/msphere.00629-24

Serotype 3 (T3) strains of mammalian orthoreovirus (reovirus) spread to the central nervous system to infect the brain and cause lethal encephalitis in newborn mice. Although reovirus targets several regions in the brain, susceptibility to infection is not uniformly distributed. The neuronal subtypes and anatomic sites targeted throughout the brain are not precisely known. Reovirus binds several attachment factors and entry receptors, including sialic acid (SA)-containing glycans and paired immunoglobulin-like receptor B (PirB). While these receptors are not required for infection of some types of neurons, reovirus engagement of these receptors can influence neuronal infection in certain contexts. To identify patterns of T3 neurotropism, we used microbial identification after passive tissue clearance and hybridization chain reaction to stain reovirus-infected cells throughout intact, optically transparent brains of newborn mice. Three-dimensional reconstructions revealed in detail the sites targeted by reovirus throughout the brain volume, including dense infection of the midbrain and hindbrain. Using reovirus mutants incapable of binding SA and mice lacking PirB expression, we found that neither SA nor PirB is required for the infection of various brain regions. However, SA may confer minor differences in infection that vary by region. Collectively, these studies indicate that many regions in the brain of newborn mice are susceptible to reovirus and that patterns of reovirus infection are not dependent on reovirus receptors SA and PirB.IMPORTANCENeurotropic viruses invade the central nervous system (CNS) and target various cell types to cause disease manifestations, such as meningitis, myelitis, or encephalitis. Infections of the CNS are often difficult to treat and can lead to lasting sequelae or death. Mammalian orthoreovirus (reovirus) causes age-dependent lethal encephalitis in many young mammals. Reovirus infects neurons in several different regions of the brain. However, the complete pattern of CNS infection is not understood. We found that reovirus targets almost all regions of the brain and that patterns of tropism are not dependent on receptors sialic acid and paired immunoglobulin-like receptor B. These studies confirm that two known reovirus receptors do not completely explain the cell types infected in brain tissue and establish strategies that can be used to understand complete patterns of viral tropism in an intact brain.