Charles Patrick Davis, MD, PhD
Dr. Charles "Pat" Davis, MD, PhD, is a board certified Emergency Medicine doctor who currently practices as a consultant and staff member for hospitals. He has a PhD in Microbiology (UT at Austin), and the MD (Univ. Texas Medical Branch, Galveston). He is a Clinical Professor (retired) in the Division of Emergency Medicine, UT Health Science Center at San Antonio, and has been the Chief of Emergency Medicine at UT Medical Branch and at UTHSCSA with over 250 publications.
Melissa Conrad Stöppler, MD
Melissa Conrad Stöppler, MD, is a U.S. board-certified Anatomic Pathologist with subspecialty training in the fields of Experimental and Molecular Pathology. Dr. Stöppler's educational background includes a BA with Highest Distinction from the University of Virginia and an MD from the University of North Carolina. She completed residency training in Anatomic Pathology at Georgetown University followed by subspecialty fellowship training in molecular diagnostics and experimental pathology.
In this Article
- Flu (influenza, conventional, H1N1, H3N2, and bird flu [H5N1]) facts
- What is flu (influenza)?
- Flu vs. cold
- Flu vs. food poisoning
- What are the causes of the flu (influenza)?
- When does flu season begin and end?
- What are flu (influenza) symptoms in adults and in children?
- Influenza A information
- What is the incubation period for the flu?
- How long is the flu contagious, and how long does the flu last?
- How do health care professionals diagnose the flu (influenza)?
- How does flu spread?
- What is the key to flu (influenza) prevention?
- Are there any nasal spray vaccine or flu shot side effects in adults or in children?
- How effective is the flu vaccine?
- Why should the flu (influenza) vaccine be taken every year?
- What are some flu treatments an individual can do at home (home remedies)?
- What types of doctors treat the flu?
- What medications treat the flu?
- What can people eat when they have the flu?
- When should a person go to the emergency department for the flu?
- Who should receive the flu vaccine, and who has the highest risk factors? When should someone get the flu shot?
- What is the prognosis for patients who get the flu? What are possible complications of the flu?
- Can the flu be deadly?
- What is the bird (avian) flu?
- Do antiviral agents protect people from the flu?
- Is it safe to get a flu shot that contains thimerosal?
- Where can people find additional information about the flu?
Flu vs. food poisoning
Although some of the symptoms of influenza may mimic those of food poisoning, others do not. Most symptoms of food poisoning include nausea, vomiting, watery diarrhea, abdominal pain, cramps, and fever. Note that the majority of food poisoning symptoms are related to the gastrointestinal tract, except for fever. The common flu signs and symptoms include fever but also include symptoms that are not typical for food poisoning, because the flu is a respiratory disease. Consequently, respiratory symptoms of nasal congestion, dry cough, and some breathing problems help distinguish the flu from food poisoning.
What are the causes of the flu (influenza)?
Influenza virus information
Influenza viruses cause the flu and are divided into three types, designated A, B, and C. Influenza A and influenza B are responsible for epidemics of respiratory illness that occur almost every winter and are often associated with increased rates of hospitalization and death. Influenza type C differs from types A and B in some important ways. Type C infection usually causes either a very mild respiratory illness or no symptoms at all; it does not cause epidemics and does not have the severe public-health impact of influenza types A and B. Efforts to control the impact of influenza are aimed at types A and B, and the remainder of this discussion will be devoted only to these two types.
Influenza viruses continually change over time, usually by mutation (change in the viral RNA). This constant changing often enables the virus to evade the immune system of the host (humans, birds, and other animals) so that the host is susceptible to changing influenza virus infections throughout life. This process works as follows: A host infected with influenza virus develops antibodies against that virus; as the virus changes, the "first" antibody no longer recognizes the "newer" virus and infection can occur because the host does not recognize the new flu virus as a problem until the infection is well under way. The first antibody developed may, in some instances, provide partial protection against infection with a new influenza virus. In 2009, almost all individuals had no antibodies that could recognize the novel H1N1 virus immediately.
Type A viruses are divided into subtypes or strains based on differences in two viral surface proteins called the hemagglutinin (H) and the neuraminidase (N). There are at least 16 known H subtypes and nine known N subtypes. These surface proteins can occur in many combinations. When spread by droplets or direct contact, the virus, if not killed by the host's immune system, replicates in the respiratory tract and damages host cells. In people who are immune compromised (for example, pregnant women, infants, cancer patients, asthma patients, people with pulmonary disease, and many others), the virus can cause viral pneumonia or stress the individual's system to make them more susceptible to bacterial infections, especially bacterial pneumonia. Both pneumonia types, viral and bacterial, can cause severe disease and sometimes death.
Antigenic shift and drift
Influenza type A viruses undergo two major kinds of changes. One is a series of mutations that occurs over time and causes a gradual evolution of the virus. This is called antigenic "drift." The other kind of change is an abrupt change in the hemagglutinin and/or the neuraminidase proteins. This is called antigenic "shift." In this case, a new subtype of the virus suddenly emerges. Type A viruses undergo both kinds of changes; influenza type B viruses change only by the more gradual process of antigenic drift and therefore do not cause pandemics.
The 2009 pandemic-causing H1N1 virus was a classic example of antigenic shift. Research showed that novel H1N1 swine flu has an RNA genome that contains five RNA strands derived from various swine flu strains, two RNA strands from bird flu (also termed avian flu) strains, and only one RNA strand from human flu strains. According to the CDC, mainly antigenic shifts over about 20 years led to the development of novel H1N1 flu virus. A diagram that illustrates both antigenic shift and drift can be found below (see Figure 2) and features influenza A types H1N1 and bird flu (H5N1), but almost every influenza A viral strain can go through these processes that changes the viral RNA. A recent flu epidemic in India was partially blamed on antigenic drift/shift.
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