Amoebiasis

Source: Wikipedia, the free encyclopedia.
Amoebiasis
Other namesAmoebic dysentery, amebiasis, entamoebiasis
diloxanide furoate, iodoquinoline[2]
Frequency~480 million[2]

Amoebiasis, or amoebic dysentery, is an infection of the

inflammation and ulceration of the colon with tissue death or perforation, which may result in peritonitis.[2] Anemia may develop due to prolonged gastric bleeding.[2]

Bacterial colitis can result in similar symptoms.[2]

Prevention of amoebiasis is by improved

diloxanide furoate or iodoquinoline.[2] Effective treatment against all stages of the disease may require a combination of medications.[2] Infections without symptoms may be treated with just one antibiotic, and infections with symptoms are treated with two antibiotics.[3]

Amoebiasis is present all over the world,

developing world.[7] About 480 million people are currently infected with about 40 million new cases per year with significant symptoms.[2][8] This results in the death of between 40,000–100,000 people a year.[4] The first case of amoebiasis was documented in 1875. In 1891, the disease was described in detail, resulting in the terms amoebic dysentery and amoebic liver abscess.[2] Further evidence from the Philippines in 1913 found that upon swallowing cysts of E. histolytica volunteers developed the disease.[2]

Signs and symptoms

Most infected people, about 90%, are asymptomatic,[9] but this disease has the potential to become serious. It is estimated that about 40,000 to 100,000 people worldwide die annually due to amoebiasis.[4]

Infections can sometimes last for years if there is no treatment. Symptoms take from a few days to a few weeks to develop and manifest themselves, but usually it is about two to four weeks. Symptoms can range from mild diarrhea to dysentery with blood, coupled with intense abdominal pains. Extra-intestinal complications might also arise as a result of invasive infection which includes colitis, liver, lung, or brain abscesses.[9] The blood comes from bleeding lesions created by the amoebae invading the lining of the colon. In about 10% of invasive cases the amoebae enter the bloodstream and may travel to other organs in the body. Most commonly this means the liver,[10] as this is where blood from the intestine reaches first, but they can end up almost anywhere in the body.[citation needed]

Onset time is highly variable and the average asymptomatic infection persists for over a year. It is theorized that the absence of symptoms or their intensity may vary with such factors as strain of amoeba, immune response of the host, and perhaps associated bacteria and viruses.[citation needed]

In asymptomatic infections, the amoeba lives by eating and digesting bacteria and food particles in the gut, a part of the

ascending colon or rectum due to long-lasting immunological cellular response, and is sometimes confused with cancer.[11]

The ingestion of one viable cyst may cause an infection.[12]

Steroid therapy can occasionally provoke severe amoebic colitis in people with any E. histolytica infection.[13] This bears high mortality: on average more than 50% with severe colitis die.[13]

Cause

Amoebiasis is an infection caused by the

.

Transmission

Life-cycle of the Entamoeba histolytica

Amoebiasis is usually transmitted by the

parasite, a semi-dormant and hardy structure found in feces. Any non-encysted amoebae, or trophozoites, die quickly after leaving the body but may also be present in stool: these are rarely the source of new infections.[9] Since amoebiasis is transmitted through contaminated food and water, it is often endemic in regions of the world with limited modern sanitation systems, including México, Central America, western South America, South Asia, and western and southern Africa.[14]

Amoebic dysentery is one form of

although most traveler's diarrhea is bacterial or viral in origin.

Pathogenesis

Tissue damage caused by E. histolytica is a result of three main events, host cell death, inflammation, and parasite invasion. Abbreviations: EhMIF, E. histolytica macrophage migration inhibitory factor; MMP, matrix metalloproteinases.

Amoebiasis results from tissue destruction induced by the E. histolytica parasite.

E. histolytica causes tissue damage by three main events: direct host cell killing, inflammation, and parasite invasion.[16] The pathogenesis of amoebiasis involves interplay of various molecules secreted by E. histolytica such as LPPG, lectins, cysteine proteases, and amoebapores. Lectins help in the attachment of the parasite to the mucosal layer of the host during invasion. The amoebapores destroy the ingested bacteria present in the colonic environment. Cysteine proteases lyse the host tissues. Other molecules such as PATMK, myosins, G proteins, C2PK, CaBP3, and EhAK1 play an important role in the process of phagocytosis.[17]

Diagnosis

With colonoscopy it is possible to detect small ulcers of between 3–5mm, but diagnosis may be difficult as the mucous membrane between these areas can look either healthy or inflamed.[2] Trophozoites may be identified at the ulcer edge or within the tissue, using immunohistochemical staining with specific anti-E. histolytica antibodies.[7]

Asymptomatic human infections are usually diagnosed by finding cysts shed in the stool. Various flotation or sedimentation procedures have been developed to recover the cysts from fecal matter and stains help to visualize the isolated cysts for microscopic examination. Since cysts are not shed constantly, a minimum of three stools are examined. In symptomatic infections, the motile form (the trophozoite) is often seen in fresh feces. Serological tests exist, and most infected individuals (with symptoms or not) test positive for the presence of antibodies. The levels of antibody are much higher in individuals with liver abscesses. Serology only becomes positive about two weeks after infection. More recent developments include a kit that detects the presence of amoeba proteins in the feces, and another that detects ameba DNA in feces. These tests are not in widespread use due to their expense.[citation needed]

Microscopy is still by far the most widespread method of diagnosis around the world. However it is not as sensitive or accurate in diagnosis as the other tests available. It is important to distinguish the E. histolytica cyst from the cysts of nonpathogenic intestinal protozoa such as

Entamoeba dispar and E. moshkovskii, are also commensals and cannot be distinguished from E. histolytica under the microscope. As E. dispar is much more common than E. histolytica in most parts of the world this means that there is a lot of incorrect diagnosis of E. histolytica infection taking place. The WHO recommends that infections diagnosed by microscopy alone should not be treated if they are asymptomatic and there is no other reason to suspect that the infection is actually E. histolytica. Detection of cysts or trophozoites stools under microscope may require examination of several samples over several days to determine if they are present, because cysts are shed intermittently and may not show up in every sample.[citation needed
]

Typically, the organism can no longer be found in the feces once the disease goes extra-intestinal.[citation needed] Serological tests are useful in detecting infection by E. histolytica if the organism goes extra-intestinal and in excluding the organism from the diagnosis of other disorders. An Ova & Parasite (O&P) test or an E. histolytica fecal antigen assay is the proper assay for intestinal infections. Since antibodies may persist for years after clinical cure, a positive serological result may not necessarily indicate an active infection. A negative serological result, however, can be equally important in excluding suspected tissue invasion by E. histolytica.[citation needed]

Stool antigen detection tests have helped to overcome some of the limitations of stool microscopy. Antigen detection tests are easy to use, but they have variable sensitivity and specificity, especially in low-endemic areas.[7]

Polymerase chain reaction (PCR) is considered the gold standard for diagnosis but remains underutilized.[7][18]

  • Immature E. histolytica/E. dispar cyst in a concentrated wet mount stained with iodine. This early cyst has only one nucleus and a glycogen mass is visible (brown stain).
    Immature E. histolytica/E. dispar cyst in a concentrated wet mount stained with iodine. This early cyst has only one nucleus and a glycogen mass is visible (brown stain).
  • Amoebae in a colon biopsy from a case of amoebic dysentery.
    Amoebae in a colon biopsy from a case of amoebic dysentery.
  • Immunohistochemical staining of trophozoites (brown) using specific anti–Entamoeba histolytica macrophage migration inhibitory factor antibodies in a patient with amebic colitis.
    Immunohistochemical staining of trophozoites (brown) using specific anti–Entamoeba histolytica macrophage migration inhibitory factor antibodies in a patient with amebic colitis.

Prevention

Specimen of the human intestine that was damaged by amebic ulcer.

To help prevent the spread of amoebiasis around the home :[citation needed]

To help prevent infection:[citation needed]

  • Avoid raw vegetables when in endemic areas, as they may have been fertilized using human feces.
  • Boil water or treat with iodine tablets.
  • Avoid eating street foods especially in public places where others are sharing sauces in one container

Good sanitary practice, as well as responsible sewage disposal or treatment, are necessary for the prevention of E. histolytica infection on an endemic level. E.histolytica cysts are usually resistant to chlorination, therefore sedimentation and filtration of water supplies are necessary to reduce the incidence of infection.[9]

E. histolytica cysts may be recovered from contaminated food by methods similar to those used for recovering

Giardia lamblia cysts from feces. Filtration is probably the most practical method for recovery from drinking water and liquid foods. E. histolytica cysts must be distinguished from cysts of other parasitic (but nonpathogenic) protozoa and from cysts of free-living protozoa as discussed above. Recovery procedures are not very accurate; cysts are easily lost or damaged beyond recognition, which leads to many falsely negative results in recovery tests.[19]

Treatment

E. histolytica infections occur in both the intestine and (in people with symptoms) in tissue of the intestine and/or liver.[14] Those with symptoms require treatment with two medications, an amoebicidal tissue-active agent and a luminal cysticidal agent.[9] Individuals that are asymptomatic only need a luminal cysticidal agent.[7]

Prognosis

Significance of Amebiasis

In the majority of cases, amoebas remain in the gastrointestinal tract of the hosts. Severe ulceration of the gastrointestinal mucosal surfaces occurs in less than 16% of cases. In fewer cases, the parasite invades the soft tissues, most commonly the liver.[10] Only rarely are masses formed (amoebomas) that lead to intestinal obstruction.(Mistaken for Ca caecum and appendicular mass) Other local complications include bloody diarrhea, pericolic and pericaecal abscess.[citation needed]

Complications of hepatic amoebiasis includes subdiaphragmatic abscess, perforation of diaphragm to pericardium and pleural cavity, perforation to abdominal cavital (amoebic peritonitis) and perforation of skin (

amoebiasis cutis).[citation needed
]

Pulmonary amoebiasis can occur from liver lesions by spread through the blood or by perforation of pleural cavity and lung. It can cause lung abscess, pulmono pleural fistula, empyema lung and broncho pleural fistula. It can also reach the brain through blood vessels and cause amoebic brain abscess and amoebic meningoencephalitis. Cutaneous amoebiasis can also occur in skin around sites of colostomy wound, perianal region, region overlying visceral lesion and at the site of drainage of liver abscess.[citation needed]

Urogenital tract amoebiasis derived from intestinal lesion can cause amoebic vulvovaginitis (May's disease), rectovesicle fistula and rectovaginal fistula.[citation needed]

Entamoeba histolytica infection is associated with malnutrition and stunting of growth in children.[20]

Epidemiology

Amoebiasis caused about 55,000 deaths worldwide in 2010, down from 68,000 in 1990.[21][22] In older textbooks it is often stated that 10% of the world's population is infected with Entamoeba histolytica.[citation needed] Nevertheless, this means that there are up to 50 million true E. histolytica infections and approximately seventy thousand die each year, mostly from liver abscesses or other complications. Although usually considered a tropical parasite, the first case reported (in 1875) was actually in St Petersburg in Russia, near the Arctic Circle.[23] Infection is more common in warmer areas, but this is because of both poorer hygiene and the parasitic cysts surviving longer in warm moist conditions.[14]

History

Amoebiasis was first described by Fedor A. Lösch in 1875, in northern Russia.

WHO in 1997 that E. histolytica was two species, despite this having first been proposed in 1925.[2] In addition to the now-recognized E. dispar, evidence shows there are at least two other species of Entamoeba that look the same in humans: E. moshkovskii and Entamoeba bangladeshi.[2] The reason these species haven't been differentiated until recently is because of the reliance on appearance.[2]

outbreak of amoebiasis in the Republic of Georgia.[26] Between 26 May and 3 September 1998, 177 cases were reported, including 71 cases of intestinal amoebiasis and 106 probable cases of liver abscess.[citation needed
]

The Nicobarese people have attested to the medicinal properties found in Glochidion calocarpum, a plant common to India, saying that its bark and seed are most effective in curing abdominal disorders associated with amoebiasis.[27]

Society and culture

An outbreak of amoebic dysentery occurs in Diana Gabaldon's novel A Breath of Snow and Ashes.[28]

References

  1. ^ "Entamoebiasis". Medical Subject Headings. National Library of Medicine. Retrieved 9 April 2024.
  2. ^ .
  3. ^ a b c "General Information | Amebiasis | Parasites | CDC". www.cdc.gov. 29 December 2021. Retrieved 13 September 2022.
  4. ^
    S2CID 203849436
    .
  5. .
  6. .
  7. ^ .
  8. .
  9. ^ .
  10. ^ .
  11. .
  12. Bad Bug Book. United States Food and Drug Administration: Center for Food Safety & Applied Nutrition. 2007-12-28. Archived
    from the original on 9 July 2009. Retrieved 2009-07-13.
  13. ^ .
  14. ^ .
  15. ^ "safewateronline.com: Travelers' Diarrhea". Archived from the original on 6 June 2008. Retrieved 2020-06-28.
  16. PMID 31008019
    .
  17. .
  18. .
  19. ^ "FDA Bacteriological Analytical Manual". Archived from the original on 2008-04-06. Retrieved 2008-03-26.
  20. PMID 16730764
    .
  21. .
  22. .
  23. .
  24. .
  25. ^ "Water and Waste Systems". Archived from the original on 2017-01-19. Retrieved 2017-01-19.[unreliable medical source?]
  26. PMID 12631887
    .
  27. .
  28. ^ "Outlandish Observations". Retrieved 2020-11-24.[unreliable medical source?]

External links