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Pages:
3 pages/β‰ˆ825 words
Sources:
2 Sources
Style:
APA
Subject:
Health, Medicine, Nursing
Type:
Research Paper
Language:
English (U.S.)
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MS Word
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Topic:

Tularemia and Hantavirus. Disease Pathology. Research Paper

Research Paper Instructions:

Tularemia and Hantavirus
I. Disease Pathology
A. Describe the characteristics of infectious agent causing diseases, including structure and toxicities. [BIO-212-01]
B. Describe lab tests used for identification of the chosen organisms.
C. Explain the mechanisms in which the diseases interfere with normal pathophysiology. Be sure to describe how the infectious agents enter the cells and establish infection in the nucleus.
D. Identify signs and symptoms of disease presentation for clinical diagnostics in support of therapeutic interventions for both diseases.
E. Describe which populations are most at risk for developing the diseases, and why. As you examine epidemiological trends, discuss how ethnographic factors (e.g., race, age, and socioeconomic class) increase risk.
F. Describe the significance and impact of the diseases on the overall communities/at large, explaining how the communities are altered.
II. Disease Management and Pharmacological Impact
A. Describe pharmacological and nonpharmacological current treatment trends used to control microbial growth for each disease, and explain how such treatments promote patient care.
B. Determine which class of drug has the most evidence to support its use in the pharmacological treatment of each disease, providing rationale.
C. Illustrate the mechanisms and principles these pharmacological treatments use to combat infection.
III. Immune Response
A. Compare innate and adaptive responses of the immune system for how it reacts to the bacteria and virus of choice.
B. Determine how microbes are detected by and adapt to the immune system for each disease. C. Explain how the immune response can be manipulated to mitigate the infections.
IV. Prevention Strategies
A. Describe current steps that are taken for prevention of infection of the diseases.
B. Explain how preventative and protective measures are applied to effectively prevent or lessen infection of the diseases, and support your explanation with research.
C. Explain how preventative and protective measures can be enhanced for each disease to effectively reduce infection rates and disease transmission, and support your explanation with research.
D. Recommend prevention programs that can be implemented for the affected populations, and support your recommendations with research.

Research Paper Sample Content Preview:

Tularemia and Hantavirus
Name
Institution
Tularemia and Hantavirus
Disease Pathology
Francisella tularensis is the leading agent causing tularemia. It is a fastidious organism. F tularensis requires cysteine to grow. CHAB- cysteine heart agar with blood, Martin Lewis, Thayer-Martin, BCYE-buffered charcoal yeast extract agar, and cysteine supports F. tularensis growth. Cysteine may be contained in the commercial sheep blood agar. SBA- sheep blood agar has a poor growth rate at 24hours (Burke, 1977). In 48-72 hours, the colonies go from 1-2 mm and then grey to white and nonhemolytic. In Cystine enriched chocolate agar, Thayer-Martin agar colonies and Martin Lewis agar it has 1-3 mm, then grey to white in 48 -72 hours. CHAB colonies form 2-4 mm, then smooth to entire to greenish white and then butyrous with a sheen that is opalescent in 48-72 hours (Burke, 1977). MacConkey agar has no growth. The agent is inert, meaning it is unable to stimulate mononuclear cells to release nitric oxide or cytokines and does not act as an endotoxin antagonist for the mononuclear cells. Thus, the agent does not interact host LPS recognition proteins. Hantavirus is caused by pathogenic old world found across Europe, Asia. They cause a fever that comes with renal syndrome. Shrews and rodents carry Bunyaviridae agents that cause Hantavirus.
Diagnosing tularemia is not easy as it is a difficult culture, an enzyme-linked immunosorbent assay and the PCR methods are utilized to identify the bacteria. CHAB such as sheep blood agars or Thayer-Martin agars is used for isolation of bacteria from the clinical specimen indicating the existence of the pathogens. Serological tests are also popular, especially among non-vaccinated practitioners. F. tularensis enters the body macrophages through cytochalasin B-insensitive pathway, and it does not trigger the respiratory burst. Tularemia symptoms vary based on how the infectious agent entered the body, however for the most common that is the Ulceroglandular signs include, skin cancer which followed by swelling in the lymph glands. A patient may get antibiotics such as gentamicin or therapy for complications such as pneumonia. PS infections flow as follows; fever, which advances to myalgia, headache, nausea, and vomiting, coughing and shortness of breath. Patients are to be put into intensive cardiopulmonary support.
There were several attempts to immunize individuals with F. tularensis LVS. There was an airborne immunization done for guinea pigs and non-humans primates. For Hantavirus any community that goes into contact with rodents saliva, urine or droppings is at risk of infection. Similar to Hantavirus, in Tularemia infect those whose work involves animals like veterinarians, those living in heavily forested area...
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