إعـــــــلان

تقليص
لا يوجد إعلان حتى الآن.

Toxoplasmosis

تقليص
X
 
  • تصفية - فلترة
  • الوقت
  • عرض
إلغاء تحديد الكل
مشاركات جديدة

  • Toxoplasmosis

    Toxoplasma gondii


    Toxoplasmosis







    History

    The organism was first described in 1908 in Tunis by Charles Nicolle and Louis Manceaux within the tissues of the gundi (Ctenodactylus gundi). In the same year it was also described in Brazil by Alfonso Splendore in rabbits .
    The protozoan was first discovered by Nicolle & Manceaux, who in 1908 isolated it from the African rodent Ctenodactylus gundi, then in 1909 differentiated the disease from Leishmania and named it Toxoplasma gondii.[18] The first recorded congenital case was not until 1923, and the first adult case not until 1940.[18] In 1948, a serological dye test was created by Sabin & Feldman, which is now the standard basis for diagnostic tests.[51]






    toxo100xbis-ic


    toxo250xbis-ic


    toxo400xbis-ic


    toxo1000xbis-ic


    Infection has two stages:
    Acute toxoplasmosis

    During acute toxoplasmosis, symptoms are often influenza-like: swollen lymph nodes, or muscle aches and pains that last for a month or more. Rarely, a patient with a fully functioning immune system may develop eye damage or nasal lesions from toxoplasmosis. Young children and immunocompromised patients, such as those with HIV/AIDS, those taking certain types of chemotherapy, or those who have recently received an organ transplant, may develop severe toxoplasmosis. This can cause damage to the brain (encephalitis) or the eyes (necrotizing retinochoroiditis). Infants infected via placental transmission may be born with either of these problems, or with nasal malformations, although these complications are rare in newborns.
    Swollen lymph nodes are more commonly found in the neck followed by axillae and then groin. Swelling may occur at different times after the initial infection, persist, and/or recur for various times independently of antiparasitic treatment.[5] It is usually found at single sites in adults, but in children multiple sites may be more common. Enlarged lymph nodes will resolve within one to two months in 60% of patients. However, a quarter of patients take 2–4 months to return to normal and 8% take 4–6 months. A substantial number of patients (6%) do not return to normal until much later.[6]
    Latent toxoplasmosis

    Most patients who become infected with Toxoplasma gondii and develop toxoplasmosis do not know it. In most immunocompetent patients, the infection enters a latent phase, during which only bradyzoites are present, forming cysts in nervous and muscle tissue. Most infants who are infected while in the womb have no symptoms at birth but may develop symptoms later in life.[7]


    Cutaneous toxoplasmosis
    While rare, skin lesions may occur in the acquired form of the disease, including roseola and erythema multiforme-like eruptions, prurigo-like nodules, urticaria, and maculopapular lesions. Newborns may have punctate macules, ecchymoses, or “blueberry muffin” lesions. Diagnosis of cutaneous toxoplasmosis is based on the tachyzoite form of T. gondii being found in the epidermis. It is found in all levels of the epidermis, is about 6 μm by 2 μm , bow-shaped, the nucleus being one-third of its size. It can be identified by electron microscopy or by Giemsa staining tissue where the cytoplasm shows blue, the nucleus red.[8]






    Possible link to psychiatric disorders:-

    Studies have been conducted that show the toxoplasmosis parasite may affect behavior and may present as or be a causative or contributory factor in various psychiatric disorders such as depression, anxiety and schizophrenia.[9][10][11] In 11 of 19 scientific studies, T. gondii antibody levels were found to be significantly higher in individuals affected by first-incidence schizophrenia than in unaffected persons. Individuals with schizophrenia are also more likely to report a clinical history of toxoplasmosis than those in the general population.[12] Recent work at the University of Leeds has found that the parasite produces an enzyme with tyrosine hydroxylase and phenylalanine hydroxylase activity. This enzyme may contribute to the behavioral changes observed in toxoplasmosis by altering the production of dopamine, a neurotransmitter involved in mood, sociability, attention, motivation and sleep patterns. Schizophrenia has long been linked to dopamine dysregulation.[13]














    Lab Diagnosis:-

    Detection of Toxoplasma gondii in human blood samples may be achieved by using the polymerase chain reaction (PCR).[14] Inactive cysts may exist in a host which would evade detection.


    [IMG]file:///C:/Users/icc/AppData/Local/Temp/msohtmlclip1/01/clip_image009.jpg[/IMG]



    [IMG]file:///C:/Users/icc/AppData/Local/Temp/msohtmlclip1/01/clip_image010.jpg[/IMG] BLOOD, BONE MARROW, SPLEEN, LYMPHNODE, [IMG]file:///C:/Users/icc/AppData/Local/Temp/msohtmlclip1/01/clip_image011.jpg[/IMG]


    CNS AND EYE PARASITES


    SPOROZOEAOrder: Eucoccidiida[IMG]file:///C:/Users/icc/AppData/Local/Temp/msohtmlclip1/01/clip_image012.jpg[/IMG]


    TOXOPLASMA GONDII


    [IMG]file:///C:/Users/icc/AppData/Local/Temp/msohtmlclip1/01/clip_image012.jpg[/IMG]





    tg1-ic



    Toxoplasma gondii:life cycle.



    [IMG]file:///C:/Users/icc/AppData/Local/Temp/msohtmlclip1/01/clip_image014.jpg[/IMG]






    tg2-ic



    T. gondii: T.gondii encephalitis (TE) is the most common cerebral


    opportunistic infection in patients with AIDS.


    The typical lesion is an ipodense focal area with ring


    contrast-enhancement and edema.


    (CT scan of a toxoplasmic encephalitis).



    [IMG]file:///C:/Users/icc/AppData/Local/Temp/msohtmlclip1/01/clip_image014.jpg[/IMG]






    tg3-ic



    T. gondii: tissue cysts, 100-300 µm, may contain up to 3.000 bradyzoites.


    The wall of mature pseudocysts is believed to represent


    a combination of host and parasitic components.



    [IMG]file:///C:/Users/icc/AppData/Local/Temp/msohtmlclip1/01/clip_image014.jpg[/IMG]






    tg4-ic



    T. gondii: diagnosis of TE is usually presumptive,


    based on clinical and radiologic findings and on the response to treatment;


    cerebral biopsy sometimes allows identification of pseudocysts in tissue sections.


    (H&E stain).



    [IMG]file:///C:/Users/icc/AppData/Local/Temp/msohtmlclip1/01/clip_image014.jpg[/IMG]






    tg4b-ic



    T. gondii: toxoplasmic pseudocyst within an inflammatory tissue reaction.


    (H&E stain).



    [IMG]file:///C:/Users/icc/AppData/Local/Temp/msohtmlclip1/01/clip_image014.jpg[/IMG]












    toxo100xbis-ic



    toxo250xbis-ic


    toxo400xbis-ic


    toxo1000xbis-ic



    T. gondii: lymphodes in Toxoplasma infection usually show expanded


    germinative centers surrounded by abundant perifollicular epithelioid cells.


    Protozoa are not commonly seen in sections, except in immunocompromised hosts:


    the patient (a 19 year old caucasian male) is in good health condition,


    without history of inherited or acquired immunodeficiency, hence this finding


    (a 16 micron pseudocysts in subcutaneous tissue of a otherwise normal scalp skin)


    is occasional and rather infrequent.



    [IMG]file:///C:/Users/icc/AppData/Local/Temp/msohtmlclip1/01/clip_image014.jpg[/IMG]






    tg5-ic



    T. gondii: the pseudocysts of T.gondii can be observed in tissue


    sections with monoclonal antibodies.



    [IMG]file:///C:/Users/icc/AppData/Local/Temp/msohtmlclip1/01/clip_image014.jpg[/IMG]






    tg6-ic



    T. gondii: direct detection of T.gondii in clinical specimens is rare;


    parasites can be isolated from blood, CSF, amniotic fluid,


    tissue biopsies on cell lines (THP-1 or MRC-5).


    In clinical specimens the presence of parasites can also


    be demonstrated by PCR analysis.



    [IMG]file:///C:/Users/icc/AppData/Local/Temp/msohtmlclip1/01/clip_image014.jpg[/IMG]






    tg7-ic



    T. gondii: intracellular trophozoites of T.gondii in a cell culture.


    The trophozoites proliferate within the vacuole developing a pseudocyst.


    (Trophozoites in a THP-1 cell, Giemsa stain).



    [IMG]file:///C:/Users/icc/AppData/Local/Temp/msohtmlclip1/01/clip_image014.jpg[/IMG]






    tg8-ic



    T. gondii: in cell cultures T.gondii proliferates to form a pseudocyst of 8-20 parasites.


    (Trophozoites in a THP-1 cell, Giemsa stain).



    [IMG]file:///C:/Users/icc/AppData/Local/Temp/msohtmlclip1/01/clip_image014.jpg[/IMG]






    tg9-ic



    T. gondii: lysis of a THP-1 cell with release of tachizoites in culture.


    (Trophozoites in a THP-1 cell, Giemsa stain).



    [IMG]file:///C:/Users/icc/AppData/Local/Temp/msohtmlclip1/01/clip_image014.jpg[/IMG]






    tgcareggi-ic



    T. gondii::intracellular trophozoites of T.gondii in a cell culture


    of human fibroblasts (MRC-5). The parasite was isolated from amniotic fluid.



    [IMG]file:///C:/Users/icc/AppData/Local/Temp/msohtmlclip1/01/clip_image014.jpg[/IMG]






    tg10-ic



    T. gondii: microscopical features of tachizoites of Toxoplasma gondii


    and peritoneal macrophages of mouse in peritoneal exudate. (SEM)



    [IMG]file:///C:/Users/icc/AppData/Local/Temp/msohtmlclip1/01/clip_image014.jpg[/IMG]






    tg11-ic



    T. gondii: microscopical features of tachizoites of Toxoplasma gondii


    and peritoneal macrophages of mouse in peritoneal exudate. (SEM)



    [IMG]file:///C:/Users/icc/AppData/Local/Temp/msohtmlclip1/01/clip_image014.jpg[/IMG]






    tg12-ic



    T. gondii: the anterior pole of an endozoid in tangential projection.


    Several subpellicular fibrils and their insertion on


    the anterior polar ring are visible.



    [IMG]file:///C:/Users/icc/AppData/Local/Temp/msohtmlclip1/01/clip_image014.jpg[/IMG]






    tg13-ic



    T. gondii: transmision electron microscopic picture.


    Longitudinal section of an endozoid.



    [IMG]file:///C:/Users/icc/AppData/Local/Temp/msohtmlclip1/01/clip_image014.jpg[/IMG]






    tg14-ic



    T. gondii: cross-section through an endozoid


    in an advanced stage of endodiogeny.


    The daugther cells appear to be surrounded.


    In each of these news cells there are two round bodies


    that lengthen forming the first rhoptries.



    [IMG]file:///C:/Users/icc/AppData/Local/Temp/msohtmlclip1/01/clip_image014.jpg[/IMG]





    [IMG]file:///C:/Users/icc/AppData/Local/Temp/msohtmlclip1/01/clip_image031.gif[/IMG]Life cycle of Toxoplasma gondii.



    life cycle of the T.gondii
    The life cycle of T. gondii has two phases. The sexual part of the life cycle (coccidia like) takes place only in members of the Felidae family (domestic and wild cats), which makes these animals the parasite's primary host. The asexual part of the life cycle can take place in any warm-blooded animal, like other mammals (including felines) and birds.


    T. gondii constructing daughter scaffolds within the mother cell.
    In the intermediate hosts (as well the definitive host, felines), the parasite invades cells, forming intracellular so-called parasitophorous vacuoles containing bradyzoites, the slowly replicating form of the parasite.[3] Vacuoles form tissue cysts mainly within the muscles and brain. Since they are within cells, the host's immune system does not detect these cysts. Resistance to antibiotics varies, but the cysts are very difficult to eradicate entirely. Within these vacuoles T. gondii propagates by endodyogeny until the infected cell eventually bursts and tachyzoites are released. Tachyzoites are the motile, asexually reproducing form of the parasite. Unlike the bradyzoites, the free tachyzoites are usually efficiently cleared by the host's immune response, although some manage to infect cells and form bradyzoites, thus maintaining the infection.
    Tissue cysts are ingested by a cat (e.g., by feeding on an infected mouse). The cysts survive passage through the stomach of the cat and the parasites infect epithelial cells of the small intestine where they undergo sexual reproduction and oocyst formation. Oocysts are shed with the feces. Animals and humans that ingest oocysts (e.g., by eating unwashed vegetables etc.) or tissue cysts in improperly cooked meat become infected. The parasite enters macrophages in the intestinal lining and is distributed via the blood stream throughout the body.
    Similar to the mechanism used in many viruses, Toxoplasma is able to dysregulate host’s cell cycle by holding cells at the G2/M border.[4] This dysregulation of the host’s cell cycle is caused by a heat-liable factor that is larger than 10kDa.[5] Infected cells secrete the factor which inhibits the cell cycle of neighboring cells. The reason for Toxoplasma’s dysregulation is unknown, but studies have shown that infection is preferential to host cells in the S-phase and host cell structures with which Toxoplasma interacts may not be accessible during other stages of the cell cycle.[6][7][8][9][10]
    Acute stage Toxoplasma infections can be asymptomatic, but often give flu-like symptoms in the early acute stages, and like flu can become, in very rare cases, fatal. The acute stage fades in a few days to months, leading to the latent stage. Latent infection is normally asymptomatic; however, in the case of immunocompromised patients (such as those infected with HIV or transplant recipients on immunosuppressive therapy), toxoplasmosis can develop. The most notable manifestation of toxoplasmosis in immunocompromised patients is toxoplasmic encephalitis, which can be deadly. If infection with T. gondii occurs for the first time during pregnancy, the parasite can cross the placenta, possibly leading to hydrocephalus or microcephaly, intracranial calcification, and chorioretinitis, with the possibility of spontaneous abortion (miscarriage) or intrauterine death.






















    Transmission:-


    Transmission may occur through:
    • Ingestion of raw or partly cooked meat, especially pork, lamb, or venison containing Toxoplasma cysts. Infection prevalence in countries where undercooked meat is traditionally eaten has been related to this transmission method. Oocysts may also be ingested during hand-to-mouth contact after handling undercooked meat, or from using knives, utensils, or cutting boards contaminated by raw meat.[15]
    • Ingestion of contaminated cat feces. This can occur through hand-to-mouth contact following gardening, cleaning a cat's litter box, contact with children's sandpits, or touching anything that has come into contact with cat feces.
    • Drinking water contaminated with Toxoplasma.
    • Transplacental infection in utero.
    • Receiving an infected organ transplant or blood transfusion, although this is extremely rare.[15]
    The cyst form of the parasite is extremely hardy, capable of surviving exposure to freezing down to −12 degrees Celsius (10 degrees Fahrenheit), moderate temperatures and chemical disinfectants such as bleach, and can survive in the environment for over a year. It is, however, susceptible to high temperatures—above 66 degrees Celsius (150 degrees Fahrenheit), and is thus killed by thorough cooking, and would be killed by 24 hours in a typical domestic freezer.[16]
    Cats excrete the pathogen in their faeces for a number of weeks after contracting the disease, generally by eating an infected rodent. Even then, cat faeces are not generally contagious for the first day or two after excretion, after which the cyst 'ripens' and becomes potentially pathogenic[citation needed]. Studies have shown that only about 2% of cats are shedding oocysts at any one time[citation needed], and that oocyst shedding does not recur even after repeated exposure to the parasite[citation needed]. Although the pathogen has been detected on the fur of cats, it has not been found in an infectious form, and direct infection from handling cats is generally believed to be very rare.[citation needed]




    Pregnancy precautions

    Congenital toxoplasmosis is a special form in which an unborn child is infected via the placenta. A positive antibody titer indicates previous exposure and immunity and largely ensures the unborn baby's safety. A simple blood draw at the first pre-natal doctor visit can determine whether or not the woman has had previous exposure and therefore whether or not she is at risk. If a woman receives her first exposure to toxoplasmosis while pregnant, the baby is at particular risk. A woman with no previous exposure should avoid handling raw meat, exposure to cat feces, and gardening (cat feces are common in garden soil). Most cats are not actively shedding oocysts and so are not a danger, but the risk may be reduced further by having the litterbox emptied daily (oocysts require longer than a single day to become infective), and by having someone else empty the litterbox. However, while risks can be minimized, they cannot be eliminated. For pregnant women with negative antibody titer, indicating no previous exposure to T. gondii, as frequent as monthly serology testing is advisable as treatment during pregnancy for those women exposed to T. gondii for the first time decreases dramatically the risk of passing the parasite to the fetus.
    Despite these risks, pregnant women are not routinely screened for toxoplasmosis in most countries (Portugal,[17]France,[18]Austria,[18] and Italy[19] being the exceptions) for reasons of cost-effectiveness and the high number of false positives generated. As invasive prenatal testing incurs some risk to the fetus (18.5 pregnancy losses per toxoplasmosis case prevented),[18]postnatal or neonatal screening is preferred. The exceptions are cases where fetal abnormalities are noted, and thus screening can be targeted.[18]
    Some regional screening programmes operate in Germany, Switzerland and Belgium.[19]
    Treatment is very important for recently infected pregnant women, to prevent infection of the fetus. Since a baby's immune system does not develop fully for the first year of life, and the resilient cysts that form throughout the body are very difficult to eradicate with anti-protozoans, an infection can be very serious in the young.






    Treatment

    Treatment is often only recommended for people with serious health problems, because the disease is most serious when one's immune system is weak.
    Acute


    Medications that are prescribed for acute toxoplasmosis are:
    an antibiotic used in combination with pyrimethamine to treat toxoplasmosis.
    an antibiotic used most often for people with HIV/AIDS.
    another option for people with problems like thrombocytopenia.
    an antibiotic used most often for pregnant women to prevent the infection of their child.
    (Other antibiotics such as minocycline have seen some use as a salvage therapy).
    Latent

    In people with latent toxoplasmosis, the cysts are immune to these treatments, as the antibiotics do not reach the bradyzoites in sufficient concentration.

    Medications that are prescribed for latent toxoplasmosis are:
    an antibiotic that has been used to kill Toxoplasma cysts inside AIDS patients.[20]
    an antibiotic which, in combination with atovaquone, seemed to optimally kill cysts in mice.[21]


    However, in latent infections successful treatment is not guaranteed, and some subspecies exhibit resistance.
    • Gold Laser Annihilation : A novel alternative treatment traps the parasite with gold nanoparticles, and then zaps them with lasers.[22]




    Biological modifications of the host

    The parasite itself can cause various effects on the host body, some of which are not fully understood.
    Reproductive changes

    A recent study has indicated toxoplasmosis correlates strongly with an increase in boy births in humans.[23] According to the researchers, "depending on the antibody concentration, the probability of the birth of a boy can increase up to a value of 0.72 ... which means that for every 260 boys born, 100 girls are born." The study also notes a mean rate of 0.608 (as opposed to the normal 0.51) for Toxoplasma-positive mothers. The study explains that this effect may not significantly influence the actual sex ratio of children born in countries with high rates of latent toxoplasmosis infection because "In high-prevalence countries, most women of reproductive age have already been infected for a long time and therefore have only low titres of anti-Toxoplasma antibodies. Our results suggest that low-titre women have similar sex ratios to Toxoplasma-negative women."[23]
    Behavioral changes

    It has been found that the parasite has the ability to change the behaviour of its host: infected rats and mice are less fearful of cats—in fact, some of the infected rats seek out cat-urine-marked areas. This effect is advantageous to the parasite, which will be able to proliferate as a cat could eat the infected rat and then reproduce. [24] The mechanism for this change is not completely understood, but there is evidence that toxoplasmosis infection raises dopamine levels and concentrates in the amygdala in infected mice.[25]
    The findings of behavioural alteration in rats and mice have led some scientists to speculate that Toxoplasma may have similar effects in humans, even in the latent phase that had previously been considered asymptomatic. Toxoplasma is one of a number of parasites that may alter their host's behaviour as a part of their life cycle.[26] The behaviors observed, if caused by the parasite, are likely due to infection and low-grade encephalitis, which is marked by the presence of cysts in the human brain, which may produce or induce production of a neurotransmitter, possibly dopamine,[27] therefore acting similarly to dopamine reuptake inhibitor type antidepressants and stimulants.

    Correlations have been found between latent Toxoplasma infections and various characteristics:[28]
    • Decreased novelty-seeking behaviour[29]
    • Slower reactions
    • Lower rule-consciousness and greater jealousy (in men)[29]
    • Promiscuity and greater conscientiousness (in women)[29]
    The evidence for behavioral effects on humans is controversial (see a collection of research papers at http://natur.cuni.cz/flegr/publ.php).[citation needed] No prospective research has been done on the topic, e.g., testing people before and after infection to ensure that the proposed behavior arises only afterwards. Although some researchers have found potentially important associations with Toxoplasma, the causal relationship, if any, is unknown, i.e., it is possible that these associations merely reflect factors that predispose certain types of people to infection. However, many of the neurobehavioral symptoms that are postulated to be due to toxoplasmosis correlate to the general function of dopamine in the human brain, and the fact that toxoplasma encodes the dopamine synthetic enzyme tyrosine hydroxylase enzymes makes it likely that neurobehavioral symptoms can result from infection.
    Studies have found that toxoplasmosis is associated with an increased car accident rate in people with Rh-negative blood. The chance of an accident relative to uninfected people is increased roughly 2.5 times.[27][30][31]
    This may be due to the slowed reaction times that are associated with infection.[30] "If our data are true then about a million people a year die just because they are infected with Toxoplasma," the researcher Jaroslav Flegr told The Guardian.[32] The data shows that the risk decreases with time after infection, but is not due to age.[27] Ruth Gilbert, medical coordinator of the European Multicentre Study on Congenital Toxoplasmosis, told BBC News Online these findings could be due to chance, or due to social and cultural factors associated with Toxoplasma infection.[33] However there is also evidence of a delayed effect which increases reaction times.[34]
    Other studies suggest that the parasite may influence personality. There are claims of Toxoplasma causing antisocial attitudes in men and promiscuity[35] (or even "signs of higher intelligence"[32] ) in women, and greater susceptibility to schizophrenia and bipolar disorder in all infected persons.[35] A 2004 study found that Toxoplasma "probably induce[s] a decrease of novelty seeking." [36]
    According to Sydney University of Technology infectious disease researcher Nicky Boulter in an article that appeared in the January/February 2007 edition of Australasian Science magazine, Toxoplasma infections lead to changes depending on the sex of the infected person. [37][38]
    The study suggests that male carriers have shorter attention spans, a greater likelihood of breaking rules and taking risks, and are more independent, anti-social, suspicious, jealous and morose. It also suggests that these men are deemed less attractive to women. Women carriers are suggested to be more outgoing, friendly, more promiscuous, and are considered more attractive to men compared with non-infected controls. The results are shown to be true when tested on mice, though it is still inconclusive. A few scientists have suggested that, if these effects are genuine, prevalence of toxoplasmosis could be a major determinant of cultural differences. [28][38][39]












    Toxoplasma's role in schizophrenia:-


    The possibility that toxoplasmosis is one cause of schizophrenia has been studied by scientists since at least 1953.[40] These studies had attracted little attention from U.S. researchers until they were publicized through the work of prominent psychiatrist and advocate E. Fuller Torrey. In 2003, Torrey published a review of this literature, reporting that almost all the studies had found that schizophrenics have elevated rates of Toxoplasma infection.[40] A 2006 paper has even suggested that prevalence of toxoplasmosis has large-scale effects on national culture.[41] These types of studies are suggestive but cannot confirm a causal relationship (because of the possibility, for example, that schizophrenia increases the likelihood of Toxoplasma infection rather than the other way around).[40]
    • Acute Toxoplasma infection sometimes leads to psychotic symptoms not unlike schizophrenia.
    • Some anti-psychotic medications that are used to treat schizophrenia, such as haloperidol, also stop the growth of Toxoplasma in cell cultures.
    • Several studies have found significantly higher levels of Toxoplasma antibodies in schizophrenia patients compared to the general population.[42]
    • Toxoplasma infection causes damage to astrocytes in the brain, and such damage is also seen in schizophrenia[citation needed].




    Epidemiology

    In humans

    The U.S. NHANES (1999–2004) national probability sample found that 10.8% of U.S. persons 6–49 years of age, and 11.0% of women 15–44 years of age, had Toxoplasma-specific IgG antibodies, indicating that they had been infected with the organism.[4] This prevalence has significantly decreased from the NHANES III (1988–1994).[43][44]
    It is estimated that between 30% and 65% of all people worldwide are infected with toxoplasmosis.[45] However, there is large variation between countries: in France, for example, around 88% of the population are carriers, probably due to a high consumption of raw and lightly cooked meat. [46] Germany, the Netherlands and Brazil also have high prevalences of around 80%, over 80%[47] and 67% respectively. In Britain about 22% are carriers, and South Korea's rate is 4.3%.[28]

    Two risk factors for contracting toxoplasmosis are:
    • Infants born to mothers who became infected with Toxoplasma for the first time during or just before pregnancy.
    • Persons with severely weakened immune systems, such as those with AIDS. Illness may result from an acute Toxoplasma infection or reactivation of an infection that occurred earlier in life.
    In other animals

    A University of California, Davis study of dead sea otters collected from 1998 to 2004 found that toxoplasmosis was the cause of death for 13% of the animals.[48] Proximity to freshwater outflows into the ocean was a major risk factor. Ingestion of oocysts from cat faeces is considered to be the most likely ultimate source.[49] According to an article in New Scientist[50] the parasites have been found in dolphins and whales. Researchers Black and Massie believe that anchovies, which travel from estuaries into the open ocean, may be helping to spread the disease.






















    LUAI ALGAHTANY LUAI2099@HOTMAIL.COM

  • #2
    اتمنى ان يكون قد نال على اعجابكم
    مع خالص امنياتي لكم بالتوفيق
    LUAI ALGAHTANY LUAI2099@HOTMAIL.COM

    تعليق


    • #3
      المشاركة الأصلية بواسطة لؤي القحطاني مشاهدة المشاركة
      اتمنى ان يكون قد نال على اعجابكم
      مع خالص امنياتي لكم بالتوفيق
      شكرا لك اخ لؤى

      اتمنالك التوفيق

      http://www.facebook.com/MkhtbrAlshjayt?ref=hl

      تعليق

      يعمل...
      X