Figure 3. HNV structure and genome

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Figure 3 Doctors leaving (Matthews, 2013, p.13.)

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Figure 3. HNV structure and genome Figure 3. HNV structure and genome. The lipid envelope of HNV virions contains the attachment (G) and fusion (F) ... Figure 3. HNV structure and genome. The lipid envelope of HNV virions contains the attachment (G) and fusion (F) glycoproteins. Matrix protein (M) forms an ordered structure beneath the membrane. The RNA genome is coated by a ribonucleoprotein complex primarily composed of nucleocapsid protein (N). Additionally, the RNA-dependent RNA polymerase (L) and phosphoprotein (P) are present. The genome of HNVs encodes six genes and nine proteins. The P gene also encodes V, W, and C proteins. V and W are produced via RNA editing in which one or two guanines are added to mRNAs at an editing site. C is produced by an alternate ribosomal start signal. Unless provided in the caption above, the following copyright applies to the content of this slide: © FEMS 2019.This article is published and distributed under the terms of the Oxford University Press, Standard Journals Publication Model (https://academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model) Pathog Dis, Volume 77, Issue 2, 15 April 2019, ftz023, https://doi.org/10.1093/femspd/ftz023 The content of this slide may be subject to copyright: please see the slide notes for details.

Figure 2. Pathology and clinical manifestation of HNV infection in humans. This figure highlights the primary features ... Figure 2. Pathology and clinical manifestation of HNV infection in humans. This figure highlights the primary features of HNV infection noted in humans. Text in white highlights pathologic findings, while red signifies clinical signs/symptoms. The primary organs affected are the brain and lungs. Infection of the brain is divided into acute and relapsed disease as the pathology and clinical presentations are distinct. Of note, NiV-M tends to present with a more encephalitic disease, while NiV-B tends to present as a primarily respiratory disease. However, aspects of both neurologic and respiratory disease are found during infection with both viruses. Unless provided in the caption above, the following copyright applies to the content of this slide: © FEMS 2019.This article is published and distributed under the terms of the Oxford University Press, Standard Journals Publication Model (https://academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model) Pathog Dis, Volume 77, Issue 2, 15 April 2019, ftz023, https://doi.org/10.1093/femspd/ftz023 The content of this slide may be subject to copyright: please see the slide notes for details.

Figure 1. Epidemiology of HNV infection of humans Figure 1. Epidemiology of HNV infection of humans. Pteropus fruit bats represent the primary reservoirs of NiV and HeV. ... Figure 1. Epidemiology of HNV infection of humans. Pteropus fruit bats represent the primary reservoirs of NiV and HeV. HeV infection on the Queensland coast occurs after horses are exposed to HeV from bats, likely via exposure to urine or partially eaten fruits. HeV then is transmitted to humans in close contact to infected horses such as veterinarians or trainers. A similar pattern is suspected for the NiV-M outbreak in the Philippines. During the Malaysia/Singapore outbreak 1998–99, NiV was transmitted to pigs, likely via partially eaten fruits. From pigs the virus infected workers on pig farms and abattoirs. Pig-to-pig transmission was also observed. NiV-B has spilled over into humans via numerous routes, but perhaps the most notable is the direct infection of humans via the consumption of date palm sap contaminated by bat urine or saliva. There has also been significant human-to-human transmission during NiV-B outbreaks. Unless provided in the caption above, the following copyright applies to the content of this slide: © FEMS 2019.This article is published and distributed under the terms of the Oxford University Press, Standard Journals Publication Model (https://academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model) Pathog Dis, Volume 77, Issue 2, 15 April 2019, ftz023, https://doi.org/10.1093/femspd/ftz023 The content of this slide may be subject to copyright: please see the slide notes for details.