Abstract
Trypanosoma brucei, the parasite, is not very common in the United States but is very common in Africa. Trypanosoma brucei is a disease that kills many people throughout Africa. Though we may not have it here it still affects people, in this paper we are going to look at the different ways T. brucei will infect people, the life cycle, the pathophysiology, the epidemiology, the signs and symptoms of the host, and last the different medicines that cure T. brucei. Trypanosoma brucei is a very serious illness and we will look how T. brucei turns into the West African trypanosomiasis and different ways to prevent getting infected by the parasite. The Africa sleeping sickness is another major thing I will be talking about, and the different
…show more content…
aspects of the disease, I will also talk about how the disease is caused, and how it could be transmitted between other people, and even embryos. Keywords: Trypanosoma brucei, T. brucei, West African trypanosomiasis, The Africa sleeping sickness. Trypanosoma brucei Trypanosoma brucei is not very common here in the United States. Not many people know about it here, but in Africa it is a very popular parasitic disease. This disease at one point was the number one mortality, which was higher than HIV (Odero, 2015, Para 5). Africa sleeping sickness is such a crazed disease, and is transmitted so easy, all it takes is for a tsetse fly with the parasite to bite you and the parasite to get in your system and you can get affected. With this parasite there are two types of this parasitic disease which are, Trypanosoma brucei gambiense and Trypanosoma brucei rhodesiense. There is a lot of confusion between these two, because they have such similar features, but they do have some different one as well. Life cycle The life cycle of Trypanosoma brucei is very unique. In the life cycle there are 8 different steps that the parasite goes through. The first four stages are in the human, and the last four stages are the tsetse fly stages. The tsetse fly is how the human in all reality gets the parasite. The first step is a tsetse fly gets a blood meal, which carries Trypanosoma brucei in it. Second step is the parasite then enters into the bloodstream trypomastigotes; then the parasite is carried in other parts of the body and other systems. The third stage is replication, the trypomastigotes is then replicated in body fluids such as blood or lymph. In the fourth stage, trypomastigotes start to invade blood, till eventually it’s in the whole blood stream. Starting now in the fifth stage it starts over on how the tsetse fly gets the disease. In the fifth stage the tsetse fly takes a blood meal from the human when it bites the human. The sixth stage the blood stream trypomastigotes transform into a procylic trypomastigotes in tsetse fly’s gut. Replication in tsetse fly is now started by binary fission. The procylic trypomastigotes then leaves the gut in stage seven and change into epimastigotes. In the final stage the epimastigotes multiply in the tsetse fly salivary glands (Biology of T. brucei, 2015, para 1). Then the cycle eventually starts over when a tsetse fly bites again and the human goes through the life cycle of the parasite again. Pathophysiology When a person is bit and infected with Trypanosoma brucei there are many changes that happen in the body. After it goes through the life cycle the parasite will continue to mature and continue to replicate. Since it starts replicating in the blood and lymph like we talked about before it starts to cause malaise, which is a sign of parasitic disease, intermittent fever, rash, and wasting. Then eventually after having T. brucei for a long period, the parasitic invasion reached the central nervous system, causing behavioral and neurological changes. Other pathophysiology may include changes in the hematologic, lymphatic, and cardiac systems. This is the reaction of immune-mediate reaction against the invaded red blood cells. A hypersensitivity may react in the skin causing problems, which may include facial edema. High levels in the spleen or lymph nodes may lead to fibrosis but rarely in to spleen failure. If not treated in time T. brucei may cause death (Odero, 2015, Para 3). Epidemiology. Though African trypanosomiasis is not common in the United States, there are still cases that are reported that were imported from Africa. Infections in travelers are very rare and is less than 1 case a year among US travelers. Most of these infections are from East Africa game parks. There may not be any cases in the US, but in 36 countries of sub-Saharan Africa it threatens millions of people (Odero, 2015, Para 5). There are two types of this parasitic disease as mentioned before, Trypanosoma brucei gambiense, which are found in 24 countries of the sub-Saharan Africa, and Trypanosoma brucei rhodesiense, which is found in 12 of the countries (Trypanosomiasis, 2016, para 3). In 1998, there was a panel of experts convened by the World Health Organization that discovered 40,000 case of African trypanosomiasis was reported and 300,000 were untreated therefore was un-diagnosed. African trypanosomiasis was considered the first or even second greatest cause of mortality in Africa, even ahead of HIV infection. This disease can happen to anyone, it does not matter if your young, old, white, black, women, or man. This disease can happen to anyone. The only thing is that when kids get it they have more severe problems, such as causing psychomotor retardation and seizure disorders (Odero, 2015, Para 5). Major Epidemics. Though we may not have this epidemic here in the United States, there have been quite a few in Africa. The latest epidemic was in 1970 and lasted about 25 years until 1995. The earliest epidemic was one between 1896 and 1906, and that was mostly in Uganda and Congo Basin (Trypanosomiasis, 2016, para 8). In the earliest epidemic there were about half a million people who were estimated to be infected. T. b. gambiense was the causative agent that they thought was the parasite but later Koerer et al proved that in fact it was T. b. rhodesiense. At that point in time there was no diagnostic features which led anyone to think that it was in fact T. b. rhodesiense (Hide, 1999, Para 8). In 1920 there was epidemic that was in many African countries. This epidemic was on its way to be bad, but mobile teams which carried screenings, test many people at risk and got them the help they needed. By the mid-1960s the disease was under control with less than 5 thousand case. This was the last case until the most recent one in 1970, there is not much information on the 1970 epidemic, but we do know that there was more than four thousand people that was infected with the disease in Uganda. (Trypanosomiasis, 2016, para 9). Transmission. Though we know that you can get Trypanosoma brucei by getting bit from tsetse fly, but there are other ways this can be transmitted. One way other than the tsetse fly you can get it is mother to child infection. This is transferred through the placenta and afect the fetus, and can cause harm or even death to the fetus. Another way is mechanical transmission through other blood sucking insects such as mosquito. One way that has been documented is sexual transmission. If two people were to have sexual intercourse the other may get the parasitic disease, which is kind of like an STD (Trypanosomiasis, 2016, para 21). Signs and Symptoms. This parasitic disease signs and symptoms can be very severe or even cause death. At the site that you are bitten, there will be a red sore that is called a chancre. Your body will start to try and stop the infection in the first 48 hours, most of the time your body will not be able to stop it. The body then starts to become feverish, you get severe body aches and headaches, irritability, fatigue, swollen lymph nodes, and joint aches. These are the common signs and symptoms of the African sleeping sickness. Some other symptoms may include skin rash, progressive confusion, personality changes, and other neurological problems once the parasite reaches the central nervous system. If left and not treated, the symptoms will become worse, and eventually death will occur within a few months (Biology of T. brucei, 2015, para 5). Diagnoses.
The way this disease is diagnosed is through the laboratory methods. The diagnosis is found on by looking at fluid or tissues by microscopy. T. b. rhodesiense is much more intense than T. b. gambiense, therefore you can find T. b. rhodesiense faster and easier, because its takes over more of the body than T. b. gambiense does. You can find T. b. rhodesiense in the blood, lymph node fluid or fluid, or a biopsy of chancre. As for T. b. gambiense you cannot find it in the blood easily, therefor is harder to diagnose. After diagnosis all patients with African sleeping sickness must have their cerebrospinal fluid examined to make sure there CNS is not in any danger because of the parasitic …show more content…
disease. Medicine and cures.
There are a few treatments for the Africa sleeping sickness, which can get rid of the parasitic disease. One of the treatment is Antitrypanosomal is indicated for all persons diagnosed with African trypanosomiasis. The parasitic disease comes in stages, and with different stages come different treatment. In the first and second stage of the disease Pentamidline, will be fused into the body 2 hours, this is with T. b. gambiense. With T. b. rhodesiense the cure in the first couple stages, you would be injected Suramin/. The only thing with these medicines are they have a lot of adverse reactions such as injection of site pain, diarrhea, nausea, and vomiting. The third stage of both is treated with Eflorithine, which is given in four daily infusions for fourteen days. The adverse effects are much more intense, which include bone marrow suppression, gastrointestinal symptoms, and seizures. For pregnant people you have to be careful, because you can hurt the fetus in embryo if you take a lot of Eflorithine. Doctors will often use this as a last resort because it may cause a lot or harm or even death to it (Resources for Health Professionals, 2013, para
2). Conclusion. Now we have talked about different aspects of Trypanosoma brucei and the different ways it harms us. The way the disease can harm people is so senseless, and it could happen to anyone. African sleeping sickness takes so many lives, and the statistics that we discussed are crazy and it is scary to think that people actually have this disease. This disease is easily transmitted through people, and it causes so many problems. We also discussed the life cycle of Trypanosoma brucei and the pathophysiology, and the epidemiology, and we can clearly see that this disease is a scary disease to carry if not treated. Though Africa may be one of the only country that this is in, the Africa Sleeping sickness is like the plague, it will be calm with no victims, but all of a sudden it takes so many people, and in some places in Africa they do not have the luxury of going to the doctor so they have to try and fight it off with the little resources they do have, and just hope for the best. This disease is a serious issue and needs to be handled immediately, because it does not discriminate, it will take many lives.
My Experiences and “The Tequila Worm” In The novel The Tequila Worm by Viola Canales we see several Mexican traditions involved, and how the character reacts towards them. In the novel we see how the Mexican traditions take a big part in the life of a young girl. Also how being attached to her family not only changes her but the whole community around. I could honestly say that I still celebrate and enjoy some of the Mexican traditions Viola Canales talks about in The Tequila Worm.
A low-grade fever, weight loss, lethargy, night sweats, respiratory congestion, cough, and hemoptysis, are symptoms indicative of Tuberculosis. A positive skin test, abnormal chest x-ray and a positive sputum culture are indicators of Tuberculosis. Tuberculosis is transmitted by inhalation of respiratory droplets containing bacteria. This excerpt depicts tuberculosis and its history and prevalence.
Treatment: Chemotherapy is on treatment method. Most infected people benefit from the treatments. To of the best drugs for treatment are Praziquantel and Oxamniquine. The side effects are mild and transient, some of then are as followed:
Several tests may be performed on patients to determine the cause of lymphatic damage and elephantiasis. A definitive diagnosis of lymphatic filariasis is done through the identification of the microfilariae in blood. Samples of blood are taken at night. Other test used for diagnosis is immunodiagnostic test; it can identify the cause of the symptoms based on the detection of antigens of Wuchereria bancrofti. This test is highly specific and sensitive, blood samples do not have to be taken at night (Seppa
This disgusting worm parasite is spread by flies and mosquitoes. The adult worm spreads its larvae throughout the host’s lymphatic system and causes the lymph nodes to become clogged up. This also makes the tissue in the host’s body to swell up and create massive muscle deformations, otherwise known as elephantiasis. The elephantiasis mainly affects the legs and genitals. The disease also affects the eyes but that can be easily detected through close inspection but it commonly causes river blindness in the host. It’s been estimated that the parasite is one of the leading causes of blindness throughout the world.
There are a number of symptoms associated with quick detection of malaria they are, being irritable, troubled sleep, poor appetite and drowsiness. Soon after people infected usua...
People of this time always had body lice and fleas. After bitten by an infected flea, nearly all victims died within three days. The early symptoms were growths the size of nuts that could grow to the size of an apple on the legs, groin, armpit, and neck. The lumps started out being red then progressed into a dark purple or a black. There wer...
This disease, often referred to as lockjaw, is a very serious illness. It is found on almost anything, but is not a common illness. This is because the disease must be transported to the lower layers of the skin and must be sealed there to incubate and grow. Tetanus causes the muscles in the body, often the arms and facial region, to contract but not have the ability to relax. It's a state of rigamortis while the person infected is still alive. The tetanus toxin is one of the most potent poisons known, yet is found in your body right now. It is often located in feces and soil, but the intestinal enzymes destroy the toxin. The mortality rate for a person infected is about 40% and that number almost doubles if the person is very young or elderly. The muscles in the chest and abdomen eventually tense up and cause the person to either stop breathing, or stops their heart. So what does a person do to prevent such an illness form happening to them? The first thing to do is get a booster shot or vaccination from the tetanus toxin. With that in place, the chance of tetanus is almost 1%. There is still a chance that the person will become infected though. So treatment has been made possible but it is still in developmental stages. The first thing that is done is the body is treated with a sort of tetanus antitoxin in conjunction with human immune globulin. This, plus a percentage of dead Tetani, cause the body to create cells capable of eliminating the toxin found outside of the intestine. Deep puncture wounds are the main source of entry for tetanus. The toxin, known as tetanospasmin, travels to the brain through the blood. If tetanus is in the body for more than 15 days, and the body registers this, then the treatment is almost useless but may cause comfort. Often, a patient will have to have an IV of penicillin and sometimes, the tissue is removed from the body. For comfort, the doctors may also give muscle relaxants. The booster shot is given for 4 years to children from age two to age six and is known as a DPT (diphtheria, pertussis, and tetanus) vaccine.
For several years, I have had an interest in virology and the spread and characteristics of various infectious diseases. Though it makes sense not to possibly induce a state of panic by informing individuals of illnesses that are not native to the area they live in and that they are not likely to contract, I have always liked to remain informed out of my own curiosity and interest. Thus, I have decided to write about malaria.
over time in order to offer a correct diagnosis, because the various symptoms must be present in
Just like the Native American’s in the new world, disease killed more people than did bullets. 4“Europeans and the Afro-Arab slave traders brought to the interior of the Congo many disease previously not known there.” The diseases that they brought to the Congo were diseases like, small pox, malaria was already known, sleeping sickness and different kinds of infections that killed millions of slaves or locals. 4“The most notorious killers were smallpox and sleeping sickness….” Most deaths were result of those two diseases, when they arrived, “the local people had no time to build up immunities.” The invaders would spread the disease throughout the interior of the village and by the time they left, the village was filled with dead bodies. The Africans called small pox, either 6“the sickness from above” or 6“the sickness from heaven”, because they didn’t know where it came from. The sleeping sickness killed hundreds of thousands of people and it spread like wildfire. “Sleeping sickness also spread lethally up the rivers. Half a million Congolese were estimated to have died of it in 1901 alone. The disease is caused by a parasite spread by the bite of the pink-striped tsetse fly, about the size of a horsefly… Once contracted by humans, sleeping sickness becomes highly
...he best anti malarial medication before travelling, use mosquito nets at all times when sleeping, and to seek early treatment if infected. Malaria unlike HIV/AIDS is curable.
Laboratory tests used to detect tuberculosis include chest x-ray, acid-fast bacilli smear and culture, and skin test known as Mantoux test. These laboratory findings will allow the clinician to recognize the stage of the disease and provide the appropriate measures that must be applied to the patient (Tamaro & Lewis, 2005).
Dr. S.M. Shamim ul Moula, “Fighting Disease” May 9, 2001 African Networks for health research and development; retrieved Dec. 9, 2003 http://www.afronets.org/archive/200105/msg00035.php
Depending on the number of parasites and the type of parasites, the type of malaria can now be determined. Antimalarials with specific infectivity suppressive action such as derivatives of artemisinin and primaquine can be prescribed to reduce malaria transmission at all intensities. For falciparum malaria, which is very lethal, the patient should be referred to a larger facility for aggressive therapy as well as parenteral antimalarials or quinine derivative malaria drugs and supportive care (Bloland & Williams, 2003, p. 57).