The virus introduces reverse transcriptase protein into the cell, which transforms RNA into DNA. This generates genetic information that the host cell can utilize to replicate the RNA virus in DNA format. Essentially, a virus consists of a protein capsule enclosing nucleic acid, which can be either DNA or RNA (with DNA being our genetic material).
The replication process of retroviruses is distinct from that of other viruses because they possess a single RNA strand and rely on reverse transcriptase to convert this RNA into DNA. In order to infect a cell, retroviruses first need to recognize and bind to a specific protein, similar to a lock and key system. This allows the virus to either fuse its lipid membrane with the cell's membrane or enter the cell through endocytosis. Once inside, the vir
...us discharges its contents and utilizes reverse transcriptase to convert its RNA into DNA. This newly formed DNA becomes integrated into the genome of the human cell.The human cell utilizes a total of 9 genes to generate proteins and RNA for virus particles. T cells, which are a type of lymphocyte or white blood cell, play a crucial role in the immune system. Killer T cells, also known as cytotoxic T lymphocytes, specifically target infected human cells with the aim of eliminating them. Helper T cells have a vital function in coordinating the immune system by providing guidance to other T cells and B cells. The absence of helper T cells leads to a significant decrease in the efficiency of both T cells and B cells.
Killer T cells, with CD8 protein, eliminate viruses. Helper T cells have CD4 protein
and command the immune system while instructing Killer T cells and B cells. However, HIV targets Helper T cells by binding its gp120 protein to the CD4 protein on their surface.
HIV does not target B Cells that lack the CD4 protein because this protein is necessary for virus binding and cell entry. If some Helper T cells remain functional, they will instruct killer T cells to eliminate infected cells. However, over time, cytotoxic cells stop responding to HIV because all Helper T cells become infected. As a result, they can no longer guide killer T cells and B cells. Furthermore, killer T cells no longer recognize HIV as foreign since it is present in all cells rather than just a few. Once the immune system becomes infected with HIV, it actively fights against the virus but cannot completely eliminate it. Instead of producing more antibodies against HIV, helper T cells – which coordinate defenses against the virus – end up serving as factories for generating more copies of the virus (source: http://www.thebody.com/h/what-happens-when-the-immune-system-is-weakened-by-hiv-infection.html).
The immune system responds to HIV infection by increasing the production of T cells, some of which develop into helper T cells. Nevertheless, as time goes on, the virus specifically attacks and infects these helper T cells, leading to their destruction. Despite continuous attempts to combat the infection and generate more T cells, there comes a stage when the body is no longer able to produce sufficient T cells. Consequently, this decrease in helper T cells leaves the body susceptible to typically harmless microorganisms like bacteria and viruses (excluding HIV).
This acquired condition of immunodeficiency is known as AIDS
(http://people. u. edu/~jbrown/hiv. html) F HIV manages to evade the immune system. HIV is gp120, a protein that recognizes and binds to a protein called CD4 present on the surface of Helper T cells. Once the virus is docked, its lipid membrane fuses with the human cell, or HIV is taken into the cell through endocytosis. Some individuals may have protection against HIV due to the presence of HLA (Human Leukocyte Antigen). If a person has HLA, their cells are especially effective at displaying fragments of HIV in a binding groove that enables killer T cells to identify and eliminate infected cells before they can act as virus replication centers.
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