Viruses: Structure, Replication, and Detection PDF

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Summary

This document provides a basic overview of viruses, their structure, how they replicate, and ways to detect them. It also details different types of viruses and the various methods used to study them, including the use of molecular techniques and antibodies. The document covers a range of topics from viral infections to the role of viral proteins.

Full Transcript

Viruses are **submicroscopic, infectious agents** Virology is **the study of viruses** Viruses are… (3): – Extremely small (e.g., 20–400 nm) – Acellular – Obligate intracellular pathogens Viruses can infect: – Bacteriophages (or phages)—viruses that infect bacteria – Animal viruses—viruses that i...

Viruses are **submicroscopic, infectious agents** Virology is **the study of viruses** Viruses are… (3): – Extremely small (e.g., 20–400 nm) – Acellular – Obligate intracellular pathogens Viruses can infect: – Bacteriophages (or phages)—viruses that infect bacteria – Animal viruses—viruses that infect animals and humans – Plant viruses—viruses that infect plants Virion: – Single, infectious virus particle – Have an exterior protective protein capsid – Contain genetic material (DNA or RNA) Capsid (3): – Protein shell that packages and protects the genome – Accounts for the bulk of a virion’s mass – Made of capsomere subunits Enveloped viruses: – Have a lipid-based envelope that surrounds the capsid – Arise from budding off the host cell (take a portion of the cell membrane with them) Naked (or nonenveloped): – Viruses lack an envelope – Arise from lysing (bursting) the host cell Viral Spikes (Peplomers): – Protrude from the viral capsid or envelope – Glycoprotein extensions that help viruses attach and gain entry to host cells – Only bind to specific factors on a given host cell Viral genes encode: – Capsomere proteins – Enzymes needed for viral replication – Structural factors Viral genomes can be either: – RNA or DNA – Single or double-stranded – Single or segmented sections – Circular or linear RNA viruses have different modes of making mRNA that the host cell will translate (2): – Single-stranded positive RNA (ssRNA +): ssRNA genome functions as an mRNA, directly translated by host cell ribosomes – Single-stranded negative RNA (ssRNA -): RNA genome is complementary to mRNA, transcribed into mRNA by RNA-dependent RNA polymerases (RdRPs) Single-stranded retroviruses: – RNA genome is made into DNA by reverse transcriptase – DNA is usually inserted into the host DNA – DNA is then transcribed into mRNA Double-stranded RNA genome (dsRNA): – Transcribed to make mRNA – Requires RNA-dependent RNA polymerases Viruses exhibit a faster rate of genomic change than do living infectious agents because: – Quick replication time – Large quantity of virions are produced – RNA genomes mutate more than DNA ▪ DNA polymerases have proofreading capabilities ▪ RNA polymerases lack proofreading Genetic changes that limit infectivity of a virus lead to **attenuated strains, which are used in vaccines** Beneficial mutations may allow the virus to: – Escape host immune system detection – Broaden host range – Expand tropism (the type of cells or tissues the virus infects) – Increase infectivity Host range refers to **a collection of species that a virus can infect** Tropism: – Refers to the tissues or cell specificity – Due to viral surface factors Some viruses can infect a wide range of host cells or tissues: **broad tropism** Other viruses can infect only one type of host cell or tissue: **narrow tropism** Viruses hijack host cell machinery to **multiply** Generalized Bacteriophage Replication (5): 1. Attachment (adsorption): Phage binds to bacterial cell 2. Penetration (entry): Phage injects genetic material into the cell 3. Replication (synthesis): Phage commandeers host cell factors to transcribe and translate viral genes 4. Assembly (maturation): Genome packed into capsid and phage structures assembled 5. Release: Bacterial cell lyses, and new phages are released Penetration (Entry) (2nd step in Generalized Animal Virus Replication): – Enveloped viruses enter through endocytosis or membrane fusion, while naked viruses enter by endocytosis Release (6th step in Generalized Animal Virus Replication): – Enveloped viruses are released by budding – Naked viruses rupture the host cell during release Acute infections: **viruses infect a host cell, and new virions are made immediately** Persistent infections: **viruses have replication strategies that allow them to avoid immune system clearance (chronic or latent)** Some viruses (e.g., HIV) form a **provirus**: integration of the viral genome into the host cell Oncogenic viruses (oncoviruses): – Viruses that can cause cancer – Cause approximately 10–15% of cancers Viruses aren’t viewable via standard light microscopy, so most detection techniques use molecular methods (3): – Identify viral genetic material – Viral proteins – Antibodies that a patient may have against viral proteins Some virus detection methods involve searching for **viral proteins** in a sample. It utilizes **purified antibodies** to bind viral antigens Agglutination tests: – Purified antibodies linked to tiny latex beads – Mixed with the sample – Antibodies bind the viral antigen – Beads agglutinate Enzyme-linked immunosorbent assays (ELISA): – Can be adapted to detect either antigens or antibodies in a sample – Target adheres to a surface – Change of color indicates binding Limitations of ELISA and Agglutination Assays: – Takes time to build up detectable antibodies ▪ Seroconversion window Detecting **viral nucleic acids** is a growing trend in diagnostics Very specific segments of viral nucleic acid are detected by: – Fluorescent-labeled probes – Sequencing – PCR (polymerase chain reaction) In most cases, antiviral drugs only **limit infections rather than cure them** Vaccines **train the immune system to recognize viruses and are an effective means to limit infection** Nucleoside analogs: **block nucleic acid replication** Interferons: **naturally occurring substances released by cells in response to viral infections** Oseltamivir (Tamiflu) and zanamivir (Relenza): **prevent influenza A and influenza B virions from budding off the host cell surface** Prions (4): – Infectious proteins; no genetic material – Do not replicate – Protein in a misfolded form triggers specific host proteins to aggregate – Cause transmissible spongiform encephalopathies (TSEs) Spongiform encephalopathies can be **inherited** or **acquired**

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