Search

Mayaro virus (MAYV) causes an acute febrile illness similar to that produced by chikungunya virus (CHIKV), an evolutionary relative in the Semliki Forest virus complex of alphaviruses. MAYV emergence is typically sporadic, but recent isolations and outbreaks indicate that the virus remains a public health concern. Given the close phylogenetic and antigenic relationship between CHIKV and MAYV, and widespread distribution of CHIKV, we hypothesized that prior CHIKV immunity may affect MAYV pathogenesis and/or influence its emergence potential. We pre-exposed immunocompetent C57BL/6 and immunocompromised A129 or IFNAR mice to wild-type CHIKV, two CHIKV vaccines, or a live-attenuated MAYV vaccine, and challenged with MAYV. We observed strong cross-protection against MAYV for mice pre-exposed to wild-type CHIKV, and moderately but significantly reduced cross-protection from CHIKV-vaccinated animals. Immunity to other alphavirus or flavivirus controls provided no protection against MAYV disease or viremia. Mechanistic studies suggested that neutralizing antibodies alone can mediate this protection, with T-cells having no significant effect on diminishing disease. Finally, human sera obtained from naturally acquired CHIKV infection cross-neutralized MAYV at high titers in vitro. Altogether, our data suggest that CHIKV infection can confer cross-protective effects against MAYV, and the resultant reduction in viremia may limit the emergence potential of MAYV. This work was supported by grants from the National Institute of Allergy and Infectious Diseases of the National Institutes of Health under Award Numbers K22AI125474 to AJA, R24AI120942 to SCW, R01 AI099123 to TW and R01AI119056 to GS. AJA is also supported by a Junior faculty award from the Institute for Critical Technology and Applied Science at Virginia Tech and by the USDA National Institute of Food and Agriculture, Hatch VA-160103, project [1020026]. EMW is supported by a doctoral fellowship from the Institute for Critical Technology and Applied Science at Virginia Tech. SRA was supported by the McLaughlin Endowment from the University of Texas Medical Branch. SLH was supported by a NIH/NRSA T32 Postdoctoral Fellowship, Center for Interdisciplinary Research in Women’s Health (CIRWH) from the National Institutes of Health.