Martinez J. Hewlett - Basic Virology

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The foundational textbook on the study of virology Basic Virology, 4th Edition This undergraduate-accessible book covers all the foundational topics in virology, including:
The basics of virology Virological techniques Molecular biology Pathogenesis of human viral disease The 4th edition includes new information on the SARS, MERS and COVID-19 coronaviruses, hepatitis C virus, influenza virus, as well as HIV and Ebola. New virological techniques including bioinformatics and advances in viral therapies for human disease are also explored in-depth. The book also includes entirely new sections on metapneumoviruses, dengue virus, and the chikungunya virus.

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While humans are often accidental targets for encephalitis viruses, it is not clear that symptoms of the disease in humans have any major role in virus spread. As with all arthropod‐borne diseases, transmission is by arthropod ingestion of blood‐associated virus found during the viremic stage of animal infection, and the behavioral effects are incidental. Still, it may be that the lethargy manifested during active disease makes infected animals more easily bitten by arthropods, and perhaps this is a factor in natural transmission.

Viral infections of the liver (viral hepatitis)

Diseases of the liver hold a special place in many types of medicine, both because of the important physiological role of this organ and because all circulating blood and lymph pass through the liver frequently. A number of different and unrelated viruses target the liver; these are collectively known as hepatitis viruses . All hepatitis viruses cause liver damage that can be devastating to the infected host. Liver failure due to hepatitis virus infections is a major reason for liver transplantation. Furthermore, a number of these viruses establish persistent carrier states in which virus is present for many months or years following infection. Currently, there are five reasonably well‐characterized human hepatitis viruses: A, B, C, delta (D), and E. The severity of the disease caused and the sequelae vary with each.

Hepatitis A

This virus is classified as a picornavirus, related to poliovirus. Hepatitis A virus (HAV) is spread by contaminated water or food, and causes a potentially severe but controllable loss of liver function and general malaise. Proper medical care will generally result in full recovery of liver function and full clearance of virus from the host, with effective immunity against reinfection. A relatively effective HAV vaccine is available for individuals at risk of infection, including those who live in, or travel to, endemic regions.

Hepatitis B

Hepatitis B virus is related to but clearly distinct from retroviruses. Unlike the situation with HAV, the B virus is spread mainly through blood, either during sexual activity or during other blood contamination events (sharing of needles, for instance), and primary infection is sometimes followed by persistent viremia and liver damage. Hepatitis B infection is a special risk to medical personnel owing to the possibility of transmission by needle stick from contaminated blood, and the virus is endemic among intravenous drug users, commercial sex workers, and their customers. The disease is also endemic in Southeast Asia, where the virus can be spread from mother to infant by birth trauma.

Hepatitis B virus infection can lead to acute disease with attendant liver failure or can be asymptomatic. In many cases, virus is completely cleared, leading to full or partial recovery of liver function. Unfortunately, 5–10% of infected individuals go on to become asymptomatic chronic carriers of the virus. Indeed, chronic hepatitis B infections are a leading factor in human liver cancer. A third form of the hepatitis B virus infection ( fulminant infection) is marked by rapid onset of extensive liver damage and often death. An effective vaccine against hepatitis B virus is now widely used to prevent infection.

Hepatitis C

Hepatitis C virus is a member of the Flaviviridae, as are several other important human pathogens including dengue virus, Zika virus, and West Nile virus. The virus is transmitted by contaminated blood and blood products, and it is thought to cause as much as 25% of acute viral hepatitis worldwide. There is no current evidence of its being efficiently spread by arthropod vectors, but this possibility cannot be ruled out. Unlike those infected with HAV, a significant proportion of victims do not mount an effective immune response to the infection and have chronic infection that can last for many years with resulting accumulated liver damage and carcinoma. New anti–hepatitis C virus medicines introduced since 2011 have greatly improved the prognosis for infected people, but no vaccine currently exists.

Hepatitis delta (D)

Hepatitis delta (D) virus is a defective virus that cannot replicate without the aid of another virus, the hepatitis B virus. Rates of hepatitis D and B virus coinfection vary widely throughout the world. Hepatitis D and B virus coinfection in the same individual, however, leads to a higher incidence of chronic liver disease than does infection with hepatitis B virus alone. Hepatitis D virus infection can be prevented by use of the hepatitis B vaccine, since hepatitis D virus replication is dependent on the presence of hepatitis B virus.

Hepatitis E

Like HAV, hepatitis E virus is spread in the developing world by contaminated water and possibly by food. It is found throughout the world and has caused significant epidemics in India and Russia through problems with drinking water. In the developed world, hepatitis E virus is spread from animal reservoirs, primarily domestic pigs. The disease caused by this virus is usually mild, but can have high mortality rates in pregnant women. Recovery from acute infection is generally complete. Chronic infection occurs in immune‐compromised individuals.

QUESTIONS FOR CHAPTER 4

1 The disease SSPE is a complication that may follow infection with measles virus. Discuss the possible mechanisms occurring during development of this rare disease.

2 What features of pathogenesis are shared by measles virus, varicella zoster virus, and variola virus?

3 What are some of the unique features of infection by rabies virus?

4 What features distinguish an acute from a persistent infection?

5 Distinguish encephalitis produced by herpesvirus from that resulting from infection with an arbovirus such as La Crosse encephalitis virus.

Problems PART I

1 This part described the various patterns of viral infection that can be observed, among them acute, persistent, and latent. What common features may exist among these three types of infection? What are the distinguishing characteristics of each of these three types of infection?

2 The five hepatitis viruses have the same tissue tropism (the liver), and yet each is in a different virus family. One of them (hepatitis D or the delta agent) is actually a defective virus, sometimes called a subviral entity.In the table below, indicate the mode of transmission of each of these agents:AgentTransmitted byHepatitis A virusHepatitis B virusHepatitis C virusHepatitis D (delta) agentHepatitis E virusWhat functions of the liver may allow all of these agents to have a common tissue tropism, despite their differing modes of transmission?

3 As part of a larger project, you have been given five unknown viruses to characterize. Your job is to determine, given the tools at your disposal, the host range and tissue tropism of these unknown viruses. You will be using two kinds of cells: human and mouse. In each case, you have a cell line that grows continuously in culture and is therefore representative of the organism, but not of a particular tissue (human: HeLa cells; mouse: L cells). In addition, you have cells that are derived from and still representative of specific tissues: muscle or neurons. For each virus, you have an assay system that indicates if the virus attaches to (“+”) or does not attach to (“−”) a particular type of cell. Using the data in the table below, determine, if possible, the host range and tissue tropism of each unknown virus.HumanMouseVirusHeLaMuscleNeuronLMuscleNeuron#1+−−−−−#2++−++−#3−−−+++#4−−−−−−#5+−+−−−Here is the report form you will send back with your results. Indicate with a check mark (✓) what your conclusions are for each of the unknown viruses.Virus#1#2#3#4#5Host rangeHumanMouseBothNeitherTissue tropismMuscleNeuronNo tropismCannot be determined from data

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