Zika Virus Is Not Uniquely Stable at Physiological Temperatures Compared to Other Flaviviruses
ABSTRACT Zika virus (ZIKV) is a flavivirus that has emerged as a global health threat due in part to its association with congenital abnormalities. Other globally relevant flaviviruses include dengue virus (DENV) and West Nile virus (WNV). High-resolution structures of ZIKV reveal many similarities...
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American Society for Microbiology
2016
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oai:doaj.org-article:0538ee7c404d4a7287022a0746f181e02021-11-15T15:50:16ZZika Virus Is Not Uniquely Stable at Physiological Temperatures Compared to Other Flaviviruses10.1128/mBio.01396-162150-7511https://doaj.org/article/0538ee7c404d4a7287022a0746f181e02016-11-01T00:00:00Zhttps://journals.asm.org/doi/10.1128/mBio.01396-16https://doaj.org/toc/2150-7511ABSTRACT Zika virus (ZIKV) is a flavivirus that has emerged as a global health threat due in part to its association with congenital abnormalities. Other globally relevant flaviviruses include dengue virus (DENV) and West Nile virus (WNV). High-resolution structures of ZIKV reveal many similarities to DENV and suggest some differences, including an extended glycan loop (D. Sirohi, Z. Chen, L. Sun, T. Klose, T. C. Pierson, et al., 352:467–470, 2016, http://dx.doi.org/10.1126/science.aaf5316) and unique interactions among envelope (E) protein residues that were proposed to confer increased virion stability and contribute mechanistically to the distinctive pathobiology of ZIKV (V. A. Kostyuchenko, E. X. Lim, S. Zhang, G. Fibriansah, T. S. Ng, et al., Nature 533:425–428, 2016, http://dx.doi.org/10.1038/nature17994). However, in the latter study, virus stability was inferred by measuring the loss of infectivity following a short incubation period. Here, we rigorously assessed the relative stability of ZIKV, DENV, and WNV by measuring changes in infectivity following prolonged incubation at physiological temperatures. At 37°C, the half-life of ZIKV was approximately twice as long as the half-life of DENV (11.8 and 5.2 h, respectively) but shorter than that of WNV (17.7 h). Incubation at 40°C accelerated the loss of ZIKV infectivity. Increasing virion maturation efficiency modestly increased ZIKV stability, as observed previously with WNV and DENV. Finally, mutations at E residues predicted to confer increased stability to ZIKV did not affect virion half-life. Our results demonstrate that ZIKV is not uniquely stable relative to other flaviviruses, suggesting that its unique pathobiology is explained by an alternative mechanism. IMPORTANCE Zika virus (ZIKV) belongs to the Flavivirus genus, which includes other clinically relevant mosquito-borne pathogens such as dengue virus (DENV) and West Nile virus (WNV). Historically, ZIKV infection was characterized by a self-limiting, mild disease, but recent outbreaks have been associated with severe clinical complications, including Guillain-Barré syndrome and microcephaly, which are atypical of other flavivirus infections. Moreover, ZIKV has been detected in saliva, urine, and semen, and it may be sexually transmitted. Analysis of a high-resolution cryo-electron microscopic reconstruction of ZIKV hypothesized that the unusual stability of this virus contributes to its distinctive pathobiology. Here, we directly compared the stability of ZIKV to that of other flaviviruses following prolonged incubation in solution at physiological temperatures. We found that the stability of multiple ZIKV strains, including those from recent outbreaks, is intermediate between that of DENV and WNV, suggesting an alternative explanation for the unique clinical manifestations of ZIKV infection.Leslie GooKimberly A. DowdAlexander R. Y. SmithRebecca S. PelcChristina R. DeMasoTheodore C. PiersonAmerican Society for MicrobiologyarticleMicrobiologyQR1-502ENmBio, Vol 7, Iss 5 (2016) |
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Microbiology QR1-502 Leslie Goo Kimberly A. Dowd Alexander R. Y. Smith Rebecca S. Pelc Christina R. DeMaso Theodore C. Pierson Zika Virus Is Not Uniquely Stable at Physiological Temperatures Compared to Other Flaviviruses |
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ABSTRACT Zika virus (ZIKV) is a flavivirus that has emerged as a global health threat due in part to its association with congenital abnormalities. Other globally relevant flaviviruses include dengue virus (DENV) and West Nile virus (WNV). High-resolution structures of ZIKV reveal many similarities to DENV and suggest some differences, including an extended glycan loop (D. Sirohi, Z. Chen, L. Sun, T. Klose, T. C. Pierson, et al., 352:467–470, 2016, http://dx.doi.org/10.1126/science.aaf5316) and unique interactions among envelope (E) protein residues that were proposed to confer increased virion stability and contribute mechanistically to the distinctive pathobiology of ZIKV (V. A. Kostyuchenko, E. X. Lim, S. Zhang, G. Fibriansah, T. S. Ng, et al., Nature 533:425–428, 2016, http://dx.doi.org/10.1038/nature17994). However, in the latter study, virus stability was inferred by measuring the loss of infectivity following a short incubation period. Here, we rigorously assessed the relative stability of ZIKV, DENV, and WNV by measuring changes in infectivity following prolonged incubation at physiological temperatures. At 37°C, the half-life of ZIKV was approximately twice as long as the half-life of DENV (11.8 and 5.2 h, respectively) but shorter than that of WNV (17.7 h). Incubation at 40°C accelerated the loss of ZIKV infectivity. Increasing virion maturation efficiency modestly increased ZIKV stability, as observed previously with WNV and DENV. Finally, mutations at E residues predicted to confer increased stability to ZIKV did not affect virion half-life. Our results demonstrate that ZIKV is not uniquely stable relative to other flaviviruses, suggesting that its unique pathobiology is explained by an alternative mechanism. IMPORTANCE Zika virus (ZIKV) belongs to the Flavivirus genus, which includes other clinically relevant mosquito-borne pathogens such as dengue virus (DENV) and West Nile virus (WNV). Historically, ZIKV infection was characterized by a self-limiting, mild disease, but recent outbreaks have been associated with severe clinical complications, including Guillain-Barré syndrome and microcephaly, which are atypical of other flavivirus infections. Moreover, ZIKV has been detected in saliva, urine, and semen, and it may be sexually transmitted. Analysis of a high-resolution cryo-electron microscopic reconstruction of ZIKV hypothesized that the unusual stability of this virus contributes to its distinctive pathobiology. Here, we directly compared the stability of ZIKV to that of other flaviviruses following prolonged incubation in solution at physiological temperatures. We found that the stability of multiple ZIKV strains, including those from recent outbreaks, is intermediate between that of DENV and WNV, suggesting an alternative explanation for the unique clinical manifestations of ZIKV infection. |
format |
article |
author |
Leslie Goo Kimberly A. Dowd Alexander R. Y. Smith Rebecca S. Pelc Christina R. DeMaso Theodore C. Pierson |
author_facet |
Leslie Goo Kimberly A. Dowd Alexander R. Y. Smith Rebecca S. Pelc Christina R. DeMaso Theodore C. Pierson |
author_sort |
Leslie Goo |
title |
Zika Virus Is Not Uniquely Stable at Physiological Temperatures Compared to Other Flaviviruses |
title_short |
Zika Virus Is Not Uniquely Stable at Physiological Temperatures Compared to Other Flaviviruses |
title_full |
Zika Virus Is Not Uniquely Stable at Physiological Temperatures Compared to Other Flaviviruses |
title_fullStr |
Zika Virus Is Not Uniquely Stable at Physiological Temperatures Compared to Other Flaviviruses |
title_full_unstemmed |
Zika Virus Is Not Uniquely Stable at Physiological Temperatures Compared to Other Flaviviruses |
title_sort |
zika virus is not uniquely stable at physiological temperatures compared to other flaviviruses |
publisher |
American Society for Microbiology |
publishDate |
2016 |
url |
https://doaj.org/article/0538ee7c404d4a7287022a0746f181e0 |
work_keys_str_mv |
AT lesliegoo zikavirusisnotuniquelystableatphysiologicaltemperaturescomparedtootherflaviviruses AT kimberlyadowd zikavirusisnotuniquelystableatphysiologicaltemperaturescomparedtootherflaviviruses AT alexanderrysmith zikavirusisnotuniquelystableatphysiologicaltemperaturescomparedtootherflaviviruses AT rebeccaspelc zikavirusisnotuniquelystableatphysiologicaltemperaturescomparedtootherflaviviruses AT christinardemaso zikavirusisnotuniquelystableatphysiologicaltemperaturescomparedtootherflaviviruses AT theodorecpierson zikavirusisnotuniquelystableatphysiologicaltemperaturescomparedtootherflaviviruses |
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