Get help now
  • Pages 3
  • Words 745
  • Views 425
  • Download

    Cite

    Cameron
    Verified writer
    Rating
    • rating star
    • rating star
    • rating star
    • rating star
    • rating star
    • 5/5
    Delivery result 2 hours
    Customers reviews 339
    Hire Writer
    +123 relevant experts are online

    H1N1 and Herpes: Microbiology Essay

    Academic anxiety?

    Get original paper in 3 hours and nail the task

    Get help now

    124 experts online

    1. Compare the replication cycles of H1N1 and Herpes simplex. -Herpes (DNA) and H1N1 (RNA) viruses both multiply in the cells cytoplasm. The major differences among the multiplication process of these viruses lie in how MRNA and viral RNA are produced. The sequence is as follows (1 and 2) are: Entry, uncodeing the viral DNA/ RNA (replication). (3) Transcription of a portion of the viral DNA. Translation follows (resulting enzymes) for multiplication of DNA/RNA. Most cases of DNA viruses early transcription is carried with the host transcriptase (some types of RNA carry their own transcriptase. (4) Then translation of the “late” viral gene occurs. (5) Synthesis of capsid proteins in the cytoplasm of the host cell. (6) Maturation of the viral DNA/RNA and capsid proteins assemble to form a complete virus from the host cell. 2. Explain how such a tremendous diversity of IGG’s can be produced by plasma cells in response to an equal diversity of antigens. -Immunoglobulins are one of two important protein molecules of the immune system that engage in the recognition of pathogens or other foreign material. Antigen recognition is a pivotal process in the immune response.

    Antigen recognition allows the immune system to recognize each antigen with tremendous specificity in order to avoid an immune response to host tissues. One way in which the immune system accomplishes this is through the production of antibodies by the B-cell. Each antibody must be able to bind specifically to one part of an antigen; therefore a vast number of unique antibodies are required. The complex mechanism of antibody creation has been estimated to be able to produce billions of different structures which accounts for the widely effective function of these molecules.

    Take blood transfusions for example, the more transfusions one has the more antibodies you gain. 3. Explain how recombinant DNA technology could possibly be used to combat HIV infections. – Recombinant DNA technology now makes it possible to clone stretches of DNA. This technology can also be used as a vaccine for HIV. The stretches of DNA that are to be cloned contain specific instructions that produce molecules that will be placed in the plasmids. The molecules that are produced stimulate the immune system to many T-cell responders that could prevent or control HIV.

    After the DNA technology is used it is a possibility that your body will have an immune response against the envelope coat. 4. Describe the characteristics of HIV that allow it to eventually defeat the immune response. – HIV is a smart virus that rewrites itself every time it replicates so that your immune system will not recognize it. Over a period of time (10 years) the immune system will run out T-cells and will not be able to fight against HIV and this will cause infections to begin to establish in your body. 5. Compare type 2 hypersensitivity with type 4 hypersensitivity. Type 2 Hypersensitivity also known as Cytotoxic Hypersensitivity is where the antibodies are produced by the immune response. These antibodies then begin to bind to antigens on the patients own cell surface. Once these are binded they are recognized as intrinsic or extrinsic. During this phase the cells can act as antigen presenting cells. Another form of Type 2 hypersensitivity is called antibody-dependent cell-mediated cytotoxicity. (The reactions ran can take hours to a day. ) Type 4 hypersensitivity which is an independent antibody and its reactions take 2 to 3 days.

    Unlike others, Type 4 hypersensitivity is not antibody mediated but is a type of cell mediated response. 6. Explain what monoclonal antibody technology is. -Monoclonal technology is a way to produce large quantities of pure antibodies. Our body releases these proteins to help fight off or counteract the effects of these antigens. When cells are combined, such as a mammalian cell and a tumor cell, it is called hybridoma. When these cells are joined a large amount of pure antibodies are produced. These monoclonal antibodies only fight molecules with little or no side effects.

    Hybridoma cells are also referred to as a fused hybrid cell because they are able to grow indefinitely in the media. 7. Explain how your immune system avoids a primary immune response to your antigens. -The antigens we have in our body are marked with MHCs. When our immune system recognizes a cell with a MHC marker it does not get attacked. Cells that are not marked with this MHC marker get attacked. Immune memory allows the antibodies to remain in circulation and mark it so that it will remember it during its next exposure in the future.

    This essay was written by a fellow student. You may use it as a guide or sample for writing your own paper, but remember to cite it correctly. Don’t submit it as your own as it will be considered plagiarism.

    Need custom essay sample written special for your assignment?

    Choose skilled expert on your subject and get original paper with free plagiarism report

    Order custom paper Without paying upfront

    H1N1 and Herpes: Microbiology Essay. (2018, Oct 22). Retrieved from https://artscolumbia.org/h1n1-and-herpes-microbiology-45655-60512/

    We use cookies to give you the best experience possible. By continuing we’ll assume you’re on board with our cookie policy

    Hi, my name is Amy 👋

    In case you can't find a relevant example, our professional writers are ready to help you write a unique paper. Just talk to our smart assistant Amy and she'll connect you with the best match.

    Get help with your paper