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Recommended: Tuberculosis
Tuberculosis is one of the major causes of death from many infectious diseases (3). Out of 9 million people who are infected with mycobacteria, about 2 million deaths occur from tuberculosis every year (3). Unfortunately, the prevalence of tuberculosis is in a continuous increase due to increased number of Human immunodeificnecy virus (HIV) patients, bacterial resistance to anti-tuberculous drugs, and growing number of recreational drug users (3). The pathogen responsible for bacterial infection, potentially causing tuberculosis, is mycobacterium tuberculosis (MTB) (2). Persons with adequate immune system can control the bacterial infection so mycobacteria remain dormant for a long time (11). In a typical tuberculous granuloma, mature macrophages accumulate around a caseous lesion to prevent mycobacteria from leaking into the extracellular matrix (11). Therefore, only those with less effective immune systems will progress to primary progressive tuberculosis (2). When a patient progresses to active tuberculosis, early signs and symptoms include extreme fatigue, weight loss, and fever (7). The inflammatory and immune responses cause wasting that involves a period of rapid fat loss and muscle loss (7). Patients eventually develop cough, blood-streaked sputum from lung abscess, as well as pleuritic chest pain from the inflamed parenchyma (7). To fight against this grave and fatal disease, number of anti-tuberculous drugs was invented in hope of finding a cure. Although some first-line drugs (Isoniazid and Rifampicin) first appeared to be effective in treating tuberculosis, these anti-tuberculous drugs have failed to eradicate all cases of tuberculosis. Instead, anti-tuberculous drugs introduced more challenges in tuberculosis treatmen...
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...different conformation than the wild-type DNA. Therefore, MTB drug resistance can be determined by measuring different electrophoresis mobility on a gel (9). Further research on drug resistance mechanisms and associated mutations can be used for diagnosis and clinical care of individual patients with tuberculosis, as well as potentially combating resistant tuberculosis.
Over many years of biomedical research, there were great advances in understanding of the epidemiology and pathogenesis of tuberculosis. However, the prevalence of tuberculosis is still remains high, mainly due to acquired or developed drug resistance in Mycobacterium tuberculosis. The increase in incidences of multidrug-resistant tuberculosis (MDR-TB) urgently suggests the development of more effective drugs, which specifically targets biochemical pathway and a stage of pathogen’s life cycle.
Drug resistance in mycobacterium tuberculosis (TB) has become a severe global health threat. The fight against TB is now facing major challenges due to the appearance of Multi-Drug Resistant Tuberculosis (MDR-TB) and more recently, the virtually untreatable Extensively Drug Resistant Tuberculosis (XDR-TB). MDR-TB are strains that are resistant to both top first-line drugs, Isoniazid and Rifampin, while XDR-TB are MDR-TB strains that are also resistant to any fluoroquinolone and one or more of 3 injectable drugs. With this new resistance, there emerges a great need to find new drugs that are as effective, yet bypass the problem of resistance. One method of research is to find new vulnerabilities of tuberculosis to use as new target sites of drugs. This method is highly expensive (Scheffler, Colmer, Tynan, Demain, & Gullo, 2013), and requires intense and lengthy research just to implicate the new target site. An alternative is to develop new drugs that work on the same already known target as the first-line drugs, but by a different mechanism, thereby bypassing the resistance of the TB to the drug.
Tuberculosis or TB, referred to by some as the White death due to the epidemic that arose in Europe that lasted two hundred years, is usually caused by in humans by a microorganism by substrains of Mycobacterium tuberculosis. It’s hard to determine the exact years in which TB first infected humans, but since the disease leaves traces on the bone in can be found in archeological record and it is believed to go all the way back to the B.C. era. Although it is hard to tell if the bone damage was truly from TB, there is research that shows that it has been around since the 17th and 18th centuries with a high number of incidences of TB, and in 1882 Dr. Robert Koch announced that his discovery of the causing factor of TB, which is Mycobacterium tuberculosis. A tuberculosis bacterium is spread through the air by an infected person speaking, coughing, or sneezing. Due to the fact the bacteria is protected by a waxy cell all, the body’s defense takes weeks to develop any kind of immunity and it allows the bacteria to exponentially multiply freely within the body. If TB it’s left untreated it will eat rapidly through many tissues, usually beginning with the lungs, lymph nodes, and kidneys. As the infection spreads to the lungs, it causes a cough and fluid between the chest wall and lungs, which leads to chest pains, severe shortness of breath, and potential heart failure. TB also infects bones and joints that can produce arthritis like pain and characteristic bone damage. Another possibility is that it may affect the fluid around the brain, causing meningitis, which can lead to fever, drowsiness, and eventually coma and death (Wingerson, 2009).
Active TB patients are IGRA positive and are symptomatic. The granuloma model: macrophages get infected in non-activated macrophages, necrosis occurs, lymphocytes also activate macrophages. MTB continue to grow and spread. The tubercles bexome liuqified and extracellular bacterial growth ensue, releases liquifed caseous material into the bronchiole causes causing and this can be transmitted tooter people.
Tuberculosis needed to be treated otherwise it can be deadly. It can affect lungs and all other parts ...
Education can be a powerful weapon in fighting tuberculosis in the United States also around the world. Today, it is encouraging how so many people know how TB contracts human and what cause drug resistant effects among those who are under TB treatment.
Antibiotic resistant strains of M. tuberculosis can hinder treatment by activating and multiplying the M. tuberculosis which will then cause a TB disease.
Although some infections are unique enough to be identified clinically, usually microbiologic laboratory methods are needed to identify the etiologic agent and diagnose microbial infection (Washington, J.A., 1996). Although we have made significant progress in our ability to diagnose and treat infectious diseases, they still remain a strong challenge to human survival, for example the disease Tuberculosis caused by a microbial infection with Mycobacterium tuberculosis accounted for one third of the worlds bacterial infections in 2010 infecting a total of 8.8 million people worldwide (Dheda et al., 2010).
The exacerbating effects and devastation caused by bacteria such as Mycobacterium,Vibrio cholerae, Bacillus anthracis, Xylophilus ampelinus, etc, is the growing threat of drug-resistance in many parts of the world. Identifying and addressing barriers to effective and timely diagnosis and treatment of drug-resistant diseases will be critical to preventing further emergence of strains of the disease with broad-spectrum resistance.
The name Tuberculosis derives from ‘tubercles’, which are present in the lymph nodes of affected animals.
Both malaria and tuberculosis are the most common infectious disease in countries like Africa and India. Two of these infectious diseases were being treated by different kinds of medicine, but then when both of them would have drug resistance towards the first-line medicine that were used to treat them, it would cause more problems. One may wonder why would there be drug resistance if the drug is used correctly; the reason on why drug resistant may occur would be because there were inappropriate uses of antimicrobial agents(4). So then, because of the drug resistance that both of this disease contain, finding a treatment wasn't very easy.
In a recent study, the diagnostic role of XpertMTB/RIF demonstrated sensitivities of 98.2% and 72.5% with smear-positive and negative TB, respectively. The tests specificity was 99.2% in patients without Tuberculosis. 26
Mycobacterium tuberculosis (MT) is a slender, rod-shaped, aerobic bacillus which causes tuberculosis. Tuberculosis (TB) is an airborn infection which is transmitted via inhaling droplet nuclei circulating in the air. These droplets are expelled from the respiratory secretion of people who have active TB through coughing, sneezing, and talking (Porth, 2011). Some bacilli stay in the upper airway and are swept out by mucus-secreting goblet cells and cilia on the surface of the airway. Others will escape from this protective mechanism to travel and settle down at alveoli (Porth, 2011). Local inflammatory reaction occurs and macrophages are cells that act as next line defense mechanism to fight with mycobacteria. First they engulf micobacteria, try to reduce their strength and ability, and kill them. In the same way they send antigen to helper T lymphocytes to initiate a cell-mediated immune response (Knechel, 2009). The infected macrophages will send produced cytokines and enzymes to breakdown mycobacteria’s protein. It is the released cytokines that attract T ly...
Untreated tuberculosis patients can pass the disease by coughing or sneezing, this fills the air with bacteria containing Mycobacterium. Inhaling these unhealthy bacteria a person can be infected with tuberculosis. “This causes the parasite to multiply in the blood, causing headaches, fever, weakness, pain in the joints, and stiffness.” (World Health Organization, 2014) People who become ill might not demonstrate signs of illness right away. Nevertheless, medication is available for tuberculosis, though this can take six to nine months and sometimes longer to be treated during the course of taking the
Mycobacterium tuberculosis has been present in the human population for thousands of years; fragments of the spinal column from Egyptian mummies from 2400 BCE show definite pathological signs of tubercular decay. Called "consumption," tuberculosis was recognized as the leading cause of mortality by 1650. Using a new staining technique, Robert Koch identified the bacterium responsible for causing consumption in 1882. While scientists finally had a target for fighting the disease, they did not have the means to treat patients; the spread of infection was controlled only by attempting to isolate patients. At the turn of the twentieth century, more than 80% of the population in the United States was infected before age 20, and tuberculosis was still the leading cause of death. The production of antibiotics in the 1940’s allowed physicians to begin effectively treating patients, leading to huge drops in the death rate of the disease. Tuberculosis is still a major cause of mortality in young adults worldwide, but is less of a problem in developed countries.
There are several ways to prevent tuberculosis. One is to control existing infections from those infected including people, pets, and cows. Unfortunately, more than 1/3 of the population has tuberculosis, making it hard to contain every case of tuberculosis. The BCG vaccine exists, but it is not very useful in countries like the US. The body’s defenses against tuberculosis are effective but fail once the immune system becomes suppressed. Antibiotics can be used to help prevent tuberculosis, but tuberculosis quickly grows resistant to antibiotics. Much needed research is being done to find a way to fight off and prevent tuberculosis.