Monday, June 3, 2019

Defences Against Pathogenic Organisms

Defences Against Pathogenic OrganismsB spieleriaDefined in the dictionary as a bacterium, virus, or other microorganism that depose puddle disease.Which can then be divided into different categories, bacterium, virus, fungus and finally protozoa.Bacteria can be in the form of many sizes and can practise such(prenominal) things as cholera and typhoid fever. The virus type of pathogens are much smaller than bacteria and have a fragment of genetic material inner(a) a protective protein coat. They are also peculiarly common of causing influenza. Fungi can look like mould and can ca expenditure such things like athletes foot. Protozoa can come in the form of contaminated food and some are parasites. They are organisms that brood in or on, certain things. A very serious example of this type, is malaria.FeaturesVirusBacteriaFungusProtozoaNutritionDo not have or need nutrition and do not eat anything aboutly are heterotrophic, which means they live from and off other organisms. Also A t an elementary level, the nutritional requirements of a bacterium such as E. coli are revealed by the cells elemental composition.Absorbs nutrients like carbohydrates (glucose, fructose, xylose, sucrose) and also starches, cellulose, hemicelluloses and proteins.Require organic materials which may be particulate matter or in solution. They are holozoic.ReproductionRely on emcee cells for the machinery needed to survive and re modernize. Once finding a host, it then looks for host cells to take over and slowly implants its genetic makeup into the cell.Reproduce by the process binary fission. Where the cells split into and divides into 2 identical daughter cells and When conditions are gold such as the right temperature and nutrients are available, some bacteria like Escherichia coli can divide every 20 minutes.Environmental conditions can make how this happens and usually sexual or asexual reproduction are the main methods. Some yeasts and funguses thrive in warm environments, and can multiply at an passing fast pace.Also may be a sexual, and also reproduction by binary fission is very common here.StructureTheir structure consists of a strand of nucleic acid, which is either DNA or RNA. Then it has something called a capsid which is a protective protein coat.Bacteria have a cell wall with no nucleus and have two types of DNA- plasmid and chromosomal.Some are unicellular but most are multicellular which have cell walls and they are do of chitin.Single celled organisms that have a cell membrane, nucleus, cytoplasm and vacuole.Sources usedBbc bitesize . (2015). Whats in a cell?. forthcoming http//www.bbc.co.uk/schools/gcsebitesize/science/add_edexcel/cells/cells1.shtml. demise accessed seventeenth touchland 2015.Chris Sherwood . (2015). How Do Viruses Reproduce?. operational http//www.ehow.com/how-does_4567511_viruses-reproduce.html. exit accessed 17th surround 2015.Constantine John Alexopoulos . (2015). Fungus . Available http//www.britannica.com/EBche cked/topic/222357/fungus/57967/Nutrition. suffer accessed 17th walk 2015.G gingham. (2014). Bacteria. Available http//www.microbiologyonline.org.uk/about-microbiology/introducing-microbes/bacteria. abide accessed 17th march 2015Kenneth Todar. (2014). Nutrition and Growth of Bacteria. Available http//textbookofbacteriology.net/nutgro.html. Last accessed 17th march 2015.Robert G Yaeger . (2015). Protozoa . Available http//www.ncbi.nlm.nih.gov/books/NBK8325/. Last accessed 17th march 2015.How does the body bear out itself against pathogens which cause infectious disease?Pathogens can innovate the body by route of transmission. People can pick up a pathogen by person to person contact with touch, saliva and contaminated blood or bodily fluids. Pathogens can also be transmitted through foods, water, insects and fomites. Food can be contaminated by unclean hands, unclean utensils, and is cross contaminated. Water can be contaminated by human or animal commode which spreads the infec tion when drank, and insects can also carry a pathogen for example malaria. Lastly fomites are actually non-living but can spread pathogens by way of bedding, toys and equip for example. A common one is also athletes foot. Airborne pathogens enter through the nose and mouth of the body as you breathe, and food pathogens enter through your mouth and then into the digestive organisation. Also they can also enter into the blood stream through vectors which is transmitted by mosquitos, fleas, ticks and contaminated needles. Breaks in the skin are also ways of entering.From the outside of the body the physical defences and barriers we have to admirer us are the skin which is a physical barrier, clot which if skin is broken the blood clots to stop any entering, sebaceous and sweet secretory organs that produce chemicals that shoot bacteria, lysozyme which is in saliva and tears that kills bacteria, mucose membranes which secretes mucous and traps pathogens, nasal hairs that remove the organisms from the air, cilia force mucus to the pharynx for swallowing, hydrochloric acid kills microorganisms, and the vagina produces lactic acid which stops growth of pathogens and has a low ph and mucous membranes that kill bacteria.If the physical barriers cannot defend against pathogens, then a second defence line takes over which is a general defence frame. Phagocytes that are white blood cells suck pathogens and macrophages which are a longer living phagocytes assistant digest the bacteria and protect the body. Substances that are produced by other proteins called complement defence proteins can serve fight pathogens, and are produced in response to knowing the presence of foreign materials in the body and burst or engulf the pathogen. Also interferons are proteins that help prevent spread of the virus, and inflammation are infected cells that produce a chemical histamine, and help more white blood cells get to the area to help fight infection.Antibodies play a spec ial part to fight pathogens as they are lymphocytes that produce antibodies as a result of antigens. These are proteins in the chemical group called immunoglobulins. Each antigen will only stimulate the production of one particular antibody that will fit into its receptor area. This is called natural active induced immunity. It is protection gained against a particular pathogen by the production of specific antibodies after the antigen on the pathogen has been detected. Pathogens are prevented from entering a host cell by antibodies binding to the antigens which are on the surface of the pathogen, and pathogens can be burst by antibodies activating the complement system. -see diagram hereT and B cells are lymphocytes, while t cells advance in the thymus gland and b cells mature in the bone marrow. The point of t cells, is that they are defenders that are worked up in the thymus gland and do not actually produce antibodies but do help to protect in other ways. They have helper t cells which recognise antigens especially macrophages that multiply and enlarge and form helper t cells that produce chemicals (interferon) that then stimulate the forming of b cells. Then they stimulate the reproduction of killer t cells. slayer t cells produce and destroy abnormal body cells and release a protein named perforin which form pores in the membranes of the cells they attack and Water and ions from the surroundings flow into the cells and burst them. This is called lysis. suppresser t cells inhibit working after the pathogen is destroyed, and memory t cells survive for a long time and stimulate memory b cells to produce antibodies. B cells work in the lymphatic system especially the spleen and lymph nodes and work on just one specific antigen and comes into contact with an antigen to then reproduce at a rapid pace which are plasma cells. They are very efficient and effective, but do only last a few days. Most b cells die within a few days like said before, but some do stay alive which are referred to as memory b cells and When the same antigen becomes present in the organism these memory B-cells are already there to begin the production of plasma cells and antibodies. Which is secondary B cell response. These are more powerful because they are produced faster, more are produced, and they are produced to a smaller amount of antigen.The primary response of the insubordinate system to infection is on the first time it is encountered and Depending on the nature of the antigen and the site of entry this response can take up to 14 days to disband and leads to the generation of memory cells with a high specificity for the inducing antigen. As soon as a foreign antigen is exposed, an even though no antibodies are produced activated b cells differentiate to plasma cells. Secondary response is the response to the antigen where there is a large production of amounts of antibodies.Memory cells help generate what type of antibodies to produce during an immu ne response. It is like a B cell that keeps a memory of the older lymphocyte that was generated when there was an immune response for a specific antigen. They act as guardians waiting for the return of the same antigen so they can recruit the immune system and mount an attack sooner and more aggressively.Sources used for this TAQ* black lovage A Ademokun. (2015). Immune Responses Primary and Secondary. Available http//www.els.net/WileyCDA/ElsArticle/refId-a0000947.html. Last accessed 17th march 2015.*bbc bitesize . (2015). Defending against infection. Available http//www.bbc.co.uk/schools/gcsebitesize/science/aqa_pre_2011/human/defendingagainstinfectionrev1.shtml. Last accessed 17th march 2015.*ico praver . (2015). Routes of Transmission. Available http//www.microbiologyonline.org.uk/about-microbiology/microbes-and-the-human-body/routes-of-transmission . Last accessed 17th march 2015.* S Detea . (2015). secondary response . Available http//thesciencedictionary.org/secondary-immune-r esponse/. Last accessed 17th march 2015.ImmunityNaturalAcquiredSimilaritiesResist a specific disease. Inflammation.Resist a specific disease. Inflammation.Involve the action of antibodies in the body somehowInvolve the action of antibodies in the body somehowTechnically use white blood cells to try and fight pathogen/ infectionTechnically use white blood cells to try and fight pathogen/ infectionDifferencesNatural is from birth, and get it from beingness born and is genetic.You acquire this immunity after exposure to a pathogen.Remains throughout your lookCan be short lived or life longThis immunity has barriers that prevent entry of foreign agentsConsists of special t and b cells and also antibodies that are in body fluidResponse is adjacentResponse can take a few days, and is not immediateSources used*Christopher Hassell. (2014). Acquired Immunity. Available http//greaterimmunity.com/Files/acquired_immunity.html. Last accessed 18th march 2015*Garland science . (2015). The immun e system in health and disease. Available http//www.ncbi.nlm.nih.gov/books/NBK27090/. Last accessed 18th march 2015References and bibliographyAlexander A Ademokun. (2015). Immune Responses Primary and Secondary. Available http//www.els.net/WileyCDA/ElsArticle/refId-a0000947.html. Last accessed 17th march 2015.Ananya Mandal. (2014). Cholera Transmission. Available http//www.news-medical.net/health/Cholera-Transmission.aspx. Last accessed 16th march 2015.Arthur Schoenstadt. (2012). Malaria Transmission. Available http//malaria.emedtv.com/malaria/malaria-transmission.html. Last accessed 16th march 2015.Bbc bitesize. (2015). Defending against infection. Available http//www.bbc.co.uk/schools/gcsebitesize/science/aqa_pre_2011/human/defendingagainstinfectionrev1.shtml. Last accessed 17th march 2015.Bbc bitesize. (2015). Whats in a cell?. Available http//www.bbc.co.uk/schools/gcsebitesize/science/add_edexcel/cells/cells1.shtml. Last accessed 17th march 2015.Centers for Disease Control and P revention. (2014). Influenza. Available http//www.cdc.gov/flu/keyfacts.htm. Last accessed 16th march 2015.Eric J. Nelson, Jason B. Harris, J. Glenn Morris, Jr, Stephen B. Calderwood Andrew Camilli. (2014). Life cycle of pathogenic Vibrio cholerae.. Available http//www.nature.com/nrmicro/journal/v7/n10/fig_tab/nrmicro2204_F2.html. Last accessed 16th march 2015.Christopher Hassell. (2014). Acquired Immunity. Available http//greaterimmunity.com/Files/acquired_immunity.html. Last accessed 18th march 2015Chris Sherwood. (2015). How Do Viruses Reproduce?. Available http//www.ehow.com/how-does_4567511_viruses-reproduce.html. Last accessed 17th march 2015.Constantine John Alexopoulos. (2015). Fungus . Available http//www.britannica.com/EBchecked/topic/222357/fungus/57967/Nutrition. Last accessed 17th march 2015.Garland science. (2015). The immune system in health and disease. Available http//www.ncbi.nlm.nih.gov/books/NBK27090/. Last accessed 18th march 2015G gingham. (2014). Bacteria. Ava ilable http//www.microbiologyonline.org.uk/about-microbiology/introducing-microbes/bacteria. Last accessed 17th march 2015Great Ormond. (2015). Infection prevention and control. Available http//www.gosh.nhs.uk/parents-and-visitors/coming-to-hospital/infection-control-and-prevention/. Last accessed 18th march 2015.Ico praver. (2015). Routes of Transmission. Available http//www.microbiologyonline.org.uk/about-microbiology/microbes-and-the-human-body/routes-of-transmission . Last accessed 17th march 2015.Kalyan Das. (2015). Influenza A life cycle.. Available http//www.nature.com/nsmb/journal/v17/n5/fig_tab/nsmb.1779_F1.html. Last accessed 16th march 2015.Kenneth Todar. (2014). Nutrition and Growth of Bacteria. Available http//textbookofbacteriology.net/nutgro.html. Last accessed 17th march 2015.Kristeen Cherney. (2014). What is Cross Infection?. Available http//www.healthline.com/health/cross-infectionOverview1. Last accessed 18th march 2015.Lisa minu. (2014). Understanding Athletes o rigination . Available http//www.webmd.com/skin-problems-and-treatments/guide/understanding-athletes-foot-basics. Last accessed 16th march 2015.Public Health England. (2015). Infection control New best practice guide will aggrandize fight against healthcare associated infections See more at http//www.buildingbetterhealthcare.co.uk/news/article_page/Infection_control_New_. Available http//www.buildingbetterhealthcare.co.uk/news/article_page/Infection_control_New_best_practice_guide_will_bolster_fight_against_healthcare_associated_infections/71006. Last accessed 18th march 2015Robert G Yaeger. (2015). Protozoa . Available http//www.ncbi.nlm.nih.gov/books/NBK8325/. Last accessed 17th march 2015.S Detea . (2015). Secondary response . Available http//thesciencedictionary.org/secondary-immune-response/. Last accessed 17th march 2015.Thomas Urbauer. (2014). What Is the Life Cycle of Tinea Pedis? . Available http//www.ehow.com/about_6513541_life-cycle-tinea-pedis_.html. Last accessed 16th march 2015.Toni Rizzo. (2015). Hospital-Acquired Infections . Available http//www.encyclopedia.com/topic/Cross_infection.aspx. Last accessed 18th march 2015WHO. (2015). 10 facts on cholera. Available http//www.who.int/features/factfiles/cholera/en/. Last accessed 16th march 2015.

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