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Chapter 19 234 Viruses In 1883, A. Mayer discovered that the sap extracted from tobacco plants infected with tobacco mosaic disease.

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Presentation on theme: "Chapter 19 234 Viruses In 1883, A. Mayer discovered that the sap extracted from tobacco plants infected with tobacco mosaic disease."— Presentation transcript:

1 Chapter Viruses In 1883, A. Mayer discovered that the sap extracted from tobacco plants infected with tobacco mosaic disease was able to cause the same disease when it was sprayed onto the healthy tobacco plants. He concluded that it was caused by a submicroscopic bacterium. A decade later, D. Ivanowsky, a Russian scientist, discovered that it was caused by tobacco mosaic virus (TMV).

2 RESULTS Extracted sap from tobacco plant with tobacco mosaic disease
Fig. 19-2 RESULTS 1 Extracted sap from tobacco plant with tobacco mosaic disease 2 Passed sap through a porcelain filter known to trap bacteria 3 Rubbed filtered sap on healthy tobacco plants Figure 19.2 What causes tobacco mosaic disease? 4 Healthy plants became infected

3 234 Characteristics of Viruses: Submicroscopic and filterable
Contain either DNA or RNA, never both Contain no enzyme system Contain no cellular organelles Obligate intracellular parasites Capsid: Capsomere (capsomer): Nucleocapsid: Polyhedron: Icosahedron: Bacteriophage:

4 Fig. 19-1 Figure 19.1 Are the tiny viruses infecting this E. coli cell alive? 0.5 µm

5 RNA DNA Membranous envelope Head RNA Capsomere DNA Capsid Tail sheath
Fig. 19-3 RNA DNA Membranous envelope Head RNA Capsomere DNA Capsid Tail sheath Capsomere of capsid Tail fiber Glycoprotein Glycoproteins 18  250 nm 70–90 nm (diameter) 80–200 nm (diameter) 80  225 nm Figure 19.3 Viral structure 20 nm 50 nm 50 nm 50 nm (a) Tobacco mosaic virus (b) Adenoviruses (c) Influenza viruses (d) Bacteriophage T4

6 235 Replication of Virus: Adsorption (Attachment):
Penetration: Injection, Fusion, Phagocytosis Eclipse phase: Replication: Assembly and Maturation: Release: Lysis Budding Exocytosis

7 VIRUS Entry and uncoating DNA Capsid Transcription and manufacture
Fig. 19-4 VIRUS Entry and uncoating 1 DNA Capsid Transcription and manufacture of capsid proteins 3 2 Replication HOST CELL Viral DNA mRNA Viral DNA Capsid proteins Figure 19.4 A simplified viral reproductive cycle Self-assembly of new virus particles and their exit from the cell 4

8 235-236 Lytic Cycle: Virulent phage: Lysogenic Cycle:
Avirulent (temperate) phage: Prophage: Lysogenic conversion is a change in the characteristic of the host cell once the cell is infected with the virus.

9 Fig 1 Attachment Figure 19.5 The lytic cycle of phage T4, a virulent phage

10 Attachment Entry of phage DNA and degradation of host DNA 1 2
Fig 1 Attachment 2 Entry of phage DNA and degradation of host DNA Figure 19.5 The lytic cycle of phage T4, a virulent phage

11 Attachment Entry of phage DNA and degradation of host DNA
Fig 1 Attachment 2 Entry of phage DNA and degradation of host DNA Figure 19.5 The lytic cycle of phage T4, a virulent phage 3 Synthesis of viral genomes and proteins

12 Attachment Entry of phage DNA and degradation of host DNA
Fig 1 Attachment 2 Entry of phage DNA and degradation of host DNA Phage assembly Figure 19.5 The lytic cycle of phage T4, a virulent phage 4 Assembly 3 Synthesis of viral genomes and proteins Head Tail Tail fibers

13 Attachment Entry of phage DNA and degradation of host DNA Release
Fig 1 Attachment 2 Entry of phage DNA and degradation of host DNA 5 Release Phage assembly Figure 19.5 The lytic cycle of phage T4, a virulent phage 4 Assembly 3 Synthesis of viral genomes and proteins Head Tail Tail fibers

14 The phage injects its DNA.
Fig. 19-6 Daughter cell with prophage Phage DNA The phage injects its DNA. Cell divisions produce population of bacteria infected with the prophage. Phage DNA circularizes. Phage Bacterial chromosome Occasionally, a prophage exits the bacterial chromosome, initiating a lytic cycle. Lytic cycle Lysogenic cycle The bacterium reproduces, copying the prophage and transmitting it to daughter cells. The cell lyses, releasing phages. Lytic cycle is induced or Lysogenic cycle is entered Figure 19.6 The lytic and lysogenic cycles of phage λ, a temperate phage Prophage New phage DNA and proteins are synthesized and assembled into phages. Phage DNA integrates into the bacterial chromosome, becoming a prophage.

15 Table 19-1 Table 1

16 Table 19-1a Table 1

17 Table 19-1b Table 1

18 238 DNA Viruses: Replication DNA DNA Assembled into mRNA Protein
Transcription DNA virus mRNA Protein Translation

19 RNA Viruses: Some RNA viruses such as poliovirus and hepatitis A virus are positive (+) or sense strand RNA viruses. They serve as mRNA which can be directly translated into proteins. The negative (-) or no sense strand RNA viruses such as influenza virus, mumps virus and rabies virus, have to be converted into positive (+) before they can be translated into proteins. The positive strand is used to make negative (-) strand which is then assembled with proteins to form negative strand RNA viruses.

20 (a) The 1918 flu pandemic (b) Influenza A H5N1 virus
Fig. 19-9 (a) The 1918 flu pandemic 0.5 µm Figure 19.9 Influenza in humans and other animals For the Discovery Video Emerging Diseases, go to Animation and Video Files. (b) Influenza A H5N1 virus (c) Vaccinating ducks

21 239 Minus (-) Plus (+) strand strand RNA RNA Assembled
Plus (+) into plus (+) strand RNA translated into Proteins strand RNA viruses

22 239 Retroviruses: RNA DNA RNA assembled into transcription RNA viruses
reverse transcriptase transcription RNA DNA RNA assembled into transcription RNA viruses translation mRNA Protein

23 Fig. 19-8 Glycoprotein Viral envelope Capsid RNA (two identical strands) Reverse transcriptase HIV Membrane of white blood cell HIV HOST CELL Reverse transcriptase Viral RNA RNA-DNA hybrid 0.25 µm HIV entering a cell DNA NUCLEUS Provirus Chromosomal DNA Figure 19.8 The reproductive cycle of HIV, the retrovirus that causes AIDS RNA genome for the next viral generation mRNA New virus New HIV leaving a cell

24 Viral envelope Glycoprotein Capsid RNA (two identical strands) Reverse
Fig. 19-8a Glycoprotein Viral envelope Capsid RNA (two identical strands) Reverse transcriptase HOST CELL HIV Reverse transcriptase Viral RNA RNA-DNA hybrid DNA NUCLEUS Provirus Chromosomal DNA RNA genome for the next viral generation Figure 19.8 The reproductive cycle of HIV, the retrovirus that causes AIDS mRNA New virus

25 Membrane of white blood cell HIV HIV entering a cell
Fig. 19-8b Membrane of white blood cell HIV Figure 19.8 The reproductive cycle of HIV, the retrovirus that causes AIDS 0.25 µm HIV entering a cell New HIV leaving a cell

26 Viruses and Cancer: DNA oncogenic viruses: Hepatitis B virus Epstein Barr virus causes Burkitt’s lymphoma Human papilloma virus RNA oncogenic viruses: HTLV-I causes adult T-cell leukemia HTLV-II causes hairy-cell leukemia

27 240 Three main hypotheses on the origin of viruses:
They are fragments of host genetic material that broke off but remained in the host cytoplasm. Their ancestors were free-living noncellular macromolecules that became parasites of the cellular organisms when the organic nutrients of the primordial seas disappeared. They are organisms that reached the extreme of evolutionary specialization for parasitism by losing all the cellular organelles.

28 241 Viroids are naked RNA viruses with no capsid. They cause cadang cadang disease in coconuts, and other diseases in chrysanthemum, potato and tomato.

29 Fig Figure Viral infection of plants

30 241 Prions are infectious proteins that contain no nucleic acid. They cause scrapie in sheep, mad cow disease in cattle, kuru disease and Creutzfeldt-Jacob disease in humans.

31 Original Prion prion Aggregates of prions New prion Normal protein
Fig Original prion Prion Aggregates of prions New prion Normal protein Figure Model for how prions propagate


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