Cannot replicate without a host and are susceptible to environmental factors such as heat, UV light, and desiccation, though some viruses like those spread via fecal-oral route are more resistant
Overcome by vectors that deliver viruses directly into the bloodstream or to subcutaneous tissues
Viral dissemination within the host
1. Direct cell-to-cell contact
2. Bloodstream spread (active or passive viraemia)
3. Nervous system spread (typically after a viraemia phase)
Viral tropism
Specificity of a virus for certain cell types influenced by factors such as the presence of specific receptors, the host cell's ability to support virus replication, physical barriers, and the host's innate immune defenses
Mechanisms of viral shedding and transmission
Horizontal (direct contact, saliva, blood, semen, and other body fluids)
Vector-borne (especially for arboviruses transmitted by insects like mosquitoes and ticks)
Vertical (from mother to child during pregnancy, childbirth, or via breast milk)
Viruses
Cannot replicate without a host and are susceptible to environmental factors such as heat, UV light, and desiccation, though some viruses like those spread via fecal-oral route are more resistant
Overcome by vectors that deliver viruses directly into the bloodstream or to subcutaneous tissues
Viral dissemination within the host
1. Direct cell-to-cell contact
2. Bloodstream spread (active or passive viraemia)
3. Nervous system spread (typically after a viraemia phase)
Viral tropism
Specificity of a virus for certain cell types influenced by factors such as the presence of specific receptors, the host cell's ability to support virus replication, physical barriers, and the host's innate immune defenses
Mechanisms of viral shedding and transmission
Horizontal (direct contact, saliva, blood, semen, and other body fluids)
Vector-borne (especially for arboviruses transmitted by insects like mosquitoes and ticks)
Vertical (from mother to child during pregnancy, childbirth, or via breast milk)
Signs and symptoms of viral infections
Fatigue and fever
Rashes
Diarrhea
Neurological signs
Diagnostic methods for viral infections
Virus culture and serology (culturing the virus in specific cell types, serological tests like ELISA)
Molecular diagnostics (PCR for DNA viruses, RT-PCR for RNA viruses)
Antiviral drugs
Target specific stages of the viral life cycle to inhibit replication, challenges include drug resistance and side effects on host cells
Development of antivirals
1. Screening potential compounds
2. Rational drug design based on viral protein structures
3. Extensive testing through clinical trials
Vaccination types
Live attenuated and inactivated vaccines
Subunit, VLP, and nucleic acid vaccines
Passive immunization and immunomodulators
Provide immediate immune protection through the administration of antibodies and substances that modify immune responses, respectively
Bacteriophages
Viruses that specifically infect prokaryotes (bacteria and archaea), typically with a high specificity for their host species or strain
Structural types of bacteriophages
Head-tail
Helical
Icosahedral
Phage replication cycle
1. Adsorption
2. Penetration
3. Transcription and translation
4. Replication
5. Assembly and release
Phage genome classes in T7
Class I (sets up the cell for phage infection)
Class II (includes genes required for DNA replication)
Class III (codes for structural components and lytic enzymes)
Lysogenic cycle
The phage genome integrates into the bacterial chromosome as a prophage, which can remain dormant until triggered by environmental factors
Lytic cycle
Characterized by the active replication of phages followed by the lysis of the host cell to release progeny phages
Medical and research applications of bacteriophages
Phage therapy
Phage typing
Phage display
Plaque assay
Used to measure virus concentration in terms of plaque-forming units (PFU) per milliliter
Quantal assay
Measure lethal doses (LD50) to determine the dose at which 50% of exposed organisms die, providing information on viral virulence
Hemagglutination
Based on the ability of certain viruses to agglutinate red blood cells, used for easy and rapid virus quantification
Techniques for studying virus structure
Electron microscopy and X-ray crystallography
Density gradient centrifugation
Techniques for detecting viruses
Serological methods (detect viral proteins using antibodies)
Viral nucleic acid detection (qPCR and sequencing)
Functional studies of viruses
Tissue culture and animal studies
Rational drug design
Ellis & Delbrück (1939) demonstrated that virus replication occurs in phases within the infected host
Luria & Delbrück (1943) showed that bacterial resistance to viruses results from spontaneous mutations rather than being induced by the viruses
Hershey & Chase (1952) confirmed that DNA, not protein, is the genetic material in phages through experiments using radioactive isotopes
Fiers et al. (1976) sequenced the genome of bacteriophage MS2, marking the beginning of molecular genetics and genomics
Virology techniques are fundamental in advancing our understanding of viruses, from basic research to clinical applications, enabling the development of strategies to combat viral diseases effectively
Poxvirus subfamilies
Chordopoxvirinae (infect vertebrates)
Entomopoxvirinae (infect invertebrates)
Poxvirus virion structure
Oval or brick-shaped, measuring between 200-400 nm, with a complex and detailed structure that includes over 100 virus-encoded proteins
External surface features ridges arranged in parallel rows, sometimes helically
Highly resistant to environmental degradation
Poxvirus genome
Linear dsDNA, unusually large for viruses, ranging from 130-375 kilobases, encoding around 200 proteins
Inverted terminal repeats (ITRs) at both ends are crucial for replication and stability
Poxvirus entry mechanism
Employs a sophisticated Entry-Fusion Complex that includes multiple protein types for attachment and membrane fusion