Amoebic liver abscess other diagnostic studies: Difference between revisions

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==Overview==
==Overview==
 
Other diagnostic studies include microscopic techniques, [[Culture media|culture]] methods, [[Isoenzyme|isoenzyme analysis]], [[antibody]] detection tests, [[antigen detection test]]s, immunochromatographic assays and [[DNA]] based diagnostic tests.<ref name="pmid14987356">{{cite journal| author=Huston CD, Haque R, Petri WA| title=Molecular-based diagnosis of Entamoeba histolytica infection. | journal=Expert Rev Mol Med | year= 1999 | volume= 1999 | issue=  | pages= 1-11 | pmid=14987356 | doi=doi:10.1017/S1462399499000599 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=14987356  }} </ref><ref name="pmid14557296">{{cite journal| author=Tanyuksel M, Petri WA| title=Laboratory diagnosis of amebiasis. | journal=Clin Microbiol Rev | year= 2003 | volume= 16 | issue= 4 | pages= 713-29 | pmid=14557296 | doi= | pmc=207118 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=14557296  }} </ref><ref name="pmid619763">{{cite journal| author=Krogstad DJ, Spencer HC, Healy GR, Gleason NN, Sexton DJ, Herron CA| title=Amebiasis: epidemiologic studies in the United States, 1971-1974. | journal=Ann Intern Med | year= 1978 | volume= 88 | issue= 1 | pages= 89-97 | pmid=619763 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=619763  }} </ref><ref name="pmid12097242">{{cite journal| author=Clark CG, Diamond LS| title=Methods for cultivation of luminal parasitic protists of clinical importance. | journal=Clin Microbiol Rev | year= 2002 | volume= 15 | issue= 3 | pages= 329-41 | pmid=12097242 | doi= | pmc=118080 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=12097242  }} </ref><ref name="pmid12097242">{{cite journal| author=Clark CG, Diamond LS| title=Methods for cultivation of luminal parasitic protists of clinical importance. | journal=Clin Microbiol Rev | year= 2002 | volume= 15 | issue= 3 | pages= 329-41 | pmid=12097242 | doi= | pmc=118080 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=12097242  }} </ref>


==Other Diagnostic Tests==
==Other Diagnostic Tests==
'''Needle aspiration'''
'''Needle aspiration'''


*Needle aspiration is used to differentiate between amoebic and pyogenic liver abscess
*Needle aspiration is used to differentiate between [[amoebic liver abscess|amoebic]] and [[pyogenic liver abscess]].
*The ultrasound and CT are used to guide percutaneous aspiration and drainage.
*The [[ultrasound]] and [[CT]] are used to guide percutaneous aspiration and drainage.
*The aspirated fluid is odorless unless secondarily infected
*The aspirated fluid is odorless unless secondarily infected.
*The pathognomonic of the aspirate is the reddish-brown anchovy paste appearance, which indicates that the abscess has been present for weeks.  
*The pathognomonic of the [[aspirate]] is the reddish-brown anchovy paste appearance, which indicates that the [[abscess]] has been present for weeks.  
*The trophozoites are present only in the wall of the abscess. Rest of abscess is composed of lysed leukocytes.  
*The [[trophozoites]] are present only in the wall of the [[abscess]]. Rest of [[abscess]] is composed of lysed [[leukocytes]].
*The aspirated fluid is sent for [[gram stain]] and [[culture]].
*Common complications associated with aspiration of liver abscess include [[infection]], [[bleeding]], accidental puncture of [[echinococcal cyst]], and [[Peritonitis|amoebic peritonitis]].  
{| class="wikitable"
{| class="wikitable"
!Laboratory Method  
!Laboratory Method  
! colspan="3" |Findings
! colspan="3" |Findings
|-
|-
| rowspan="2" |Microscopy
| rowspan="2" |[[Microscopy]]
| colspan="3" |
| colspan="3" |
* Microscopic techniques include  1. Wet preparation 2. Concentration 3. Permanently stained smears<ref name="pmid14987356">{{cite journal| author=Huston CD, Haque R, Petri WA| title=Molecular-based diagnosis of Entamoeba histolytica infection. | journal=Expert Rev Mol Med | year= 1999 | volume= 1999 | issue=  | pages= 1-11 | pmid=14987356 | doi=doi:10.1017/S1462399499000599 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=14987356  }} </ref>
*Microscopic techniques include  1. Wet preparation 2. Concentration 3. Permanently stained smears<ref name="pmid14987356">{{cite journal| author=Huston CD, Haque R, Petri WA| title=Molecular-based diagnosis of Entamoeba histolytica infection. | journal=Expert Rev Mol Med | year= 1999 | volume= 1999 | issue=  | pages= 1-11 | pmid=14987356 | doi=doi:10.1017/S1462399499000599 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=14987356  }} </ref>
* Less reliable method than culture or antigen detection test<ref name="pmid14557296">{{cite journal| author=Tanyuksel M, Petri WA| title=Laboratory diagnosis of amebiasis. | journal=Clin Microbiol Rev | year= 2003 | volume= 16 | issue= 4 | pages= 713-29 | pmid=14557296 | doi= | pmc=207118 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=14557296  }} </ref><ref name="pmid619763">{{cite journal| author=Krogstad DJ, Spencer HC, Healy GR, Gleason NN, Sexton DJ, Herron CA| title=Amebiasis: epidemiologic studies in the United States, 1971-1974. | journal=Ann Intern Med | year= 1978 | volume= 88 | issue= 1 | pages= 89-97 | pmid=619763 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=619763  }} </ref>
*Less reliable method than culture or [[antigen]] detection test<ref name="pmid14557296">{{cite journal| author=Tanyuksel M, Petri WA| title=Laboratory diagnosis of amebiasis. | journal=Clin Microbiol Rev | year= 2003 | volume= 16 | issue= 4 | pages= 713-29 | pmid=14557296 | doi= | pmc=207118 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=14557296  }} </ref><ref name="pmid619763">{{cite journal| author=Krogstad DJ, Spencer HC, Healy GR, Gleason NN, Sexton DJ, Herron CA| title=Amebiasis: epidemiologic studies in the United States, 1971-1974. | journal=Ann Intern Med | year= 1978 | volume= 88 | issue= 1 | pages= 89-97 | pmid=619763 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=619763  }} </ref>
* Minimum three stool samples are examined for ova and parasites within 10days of sample collection as  organisms  are excreted intermittently<ref name="pmid8863036">{{cite journal| author=Li E, Stanley SL| title=Protozoa. Amebiasis. | journal=Gastroenterol Clin North Am | year= 1996 | volume= 25 | issue= 3 | pages= 471-92 | pmid=8863036 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=8863036  }} </ref>
*Minimum three stool samples are examined for [[ova]] and [[parasites]] within 10days of sample collection as  [[organisms]] are excreted intermittently<ref name="pmid8863036">{{cite journal| author=Li E, Stanley SL| title=Protozoa. Amebiasis. | journal=Gastroenterol Clin North Am | year= 1996 | volume= 25 | issue= 3 | pages= 471-92 | pmid=8863036 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=8863036  }} </ref>
* Presence of RBCs in trophozoites is diagnostic of Entamoeba histolytica
*Presence of [[RBC|RBCs]] in [[trophozoites]] is diagnostic of ''[[Entamoeba histolytica]]''
* The specificity of the test is low as the trophozoites containing RBCs are not present in all cases and E dispar may also contain RBCs in trophozoites<ref name="pmid8163695">{{cite journal| author=González-Ruiz A, Haque R, Aguirre A, Castañón G, Hall A, Guhl F et al.| title=Value of microscopy in the diagnosis of dysentery associated with invasive Entamoeba histolytica. | journal=J Clin Pathol | year= 1994 | volume= 47 | issue= 3 | pages= 236-9 | pmid=8163695 | doi= | pmc=501902 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=8163695  }} </ref><ref name="pmid2894495">{{cite journal| author=Strachan WD, Chiodini PL, Spice WM, Moody AH, Ackers JP| title=Immunological differentiation of pathogenic and non-pathogenic isolates of Entamoeba histolytica. | journal=Lancet | year= 1988 | volume= 1 | issue= 8585 | pages= 561-3 | pmid=2894495 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=2894495  }} </ref>
*The [[specificity]] of the test is low as the [[trophozoites]] containing [[RBC|RBCs]] are not present in all cases and ''[[Entamoeba|E dispar]]'' may also contain [[RBC|RBCs]] in [[trophozoites]].<ref name="pmid8163695">{{cite journal| author=González-Ruiz A, Haque R, Aguirre A, Castañón G, Hall A, Guhl F et al.| title=Value of microscopy in the diagnosis of dysentery associated with invasive Entamoeba histolytica. | journal=J Clin Pathol | year= 1994 | volume= 47 | issue= 3 | pages= 236-9 | pmid=8163695 | doi= | pmc=501902 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=8163695  }} </ref><ref name="pmid2894495">{{cite journal| author=Strachan WD, Chiodini PL, Spice WM, Moody AH, Ackers JP| title=Immunological differentiation of pathogenic and non-pathogenic isolates of Entamoeba histolytica. | journal=Lancet | year= 1988 | volume= 1 | issue= 8585 | pages= 561-3 | pmid=2894495 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=2894495 }} </ref>
*Freezing a fresh fecal specimen at -20°C before extraction of [[DNA]] will not effect the [[sensitivity]] of the molecular assays.<ref name="pmid17229864">{{cite journal| author=Fotedar R, Stark D, Beebe N, Marriott D, Ellis J, Harkness J| title=PCR detection of Entamoeba histolytica, Entamoeba dispar, and Entamoeba moshkovskii in stool samples from Sydney, Australia. | journal=J Clin Microbiol | year= 2007 | volume= 45 | issue= 3 | pages= 1035-7 | pmid=17229864 | doi=10.1128/JCM.02144-06 | pmc=1829108 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=17229864  }} </ref><ref name="pmid16126570">{{cite journal| author=Lebbad M, Svärd SG| title=PCR differentiation of Entamoeba histolytica and Entamoeba dispar from patients with amoeba infection initially diagnosed by microscopy. | journal=Scand J Infect Dis | year= 2005 | volume= 37 | issue= 9 | pages= 680-5 | pmid=16126570 | doi=10.1080/00365540510037812 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=16126570  }} </ref><ref name="pmid11463120">{{cite journal| author=Núñez YO, Fernández MA, Torres-Núñez D, Silva JA, Montano I, Maestre JL et al.| title=Multiplex polymerase chain reaction amplification and differentiation of Entamoeba histolytica and Entamoeba dispar DNA from stool samples. | journal=Am J Trop Med Hyg | year= 2001 | volume= 64 | issue= 5-6 | pages= 293-7 | pmid=11463120 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=11463120 }} </ref>
|-
|-
|'''Wet (Saline) preparation'''
|'''Wet (Saline) preparation'''
* Very insensitive method (<10%) Procedure
*Very insensitive method (<10%) Procedure
* The sample is a fresh specimen that should be examined within 1 hr of collection
*The sample is a fresh specimen that should be examined within 1 hr of collection
* The test is positive when RBCs in trophozoites are detected
*The test is positive when [[RBC|RBCs]] in [[trophozoites]] are detected
* It is not used in patients without acute dysentery as trophozoites will not contain RBCs  
*It is not used in patients without acute [[dysentery]] as [[trophozoites]] will not contain [[RBC|RBCs]]
|'''Concentration Technique'''
|'''Concentration Technique'''
* It is helpful in detecting cysts in the stool sample in asymptomatic carriers
* It is helpful in detecting [[cysts]] in the stool sample in asymptomatic carriers
|'''Permanently stained smears'''
|'''Permanently stained smears'''
* This is an important method for identification and recovery of Entamoeba species
*This is an important method for identification and recovery of ''[[Entamoeba|Entamoeba species]]
|-
|-
|Culture Methods
|Culture Methods
| colspan="3" |
| colspan="3" |
* The specimens for the culture of E histolytica include fecal specimens, rectal biopsy specimens or liver abscess aspirates.
*The specimens for the culture of ''[[Entamoeba|E histolytica]] include [[feces|fecal]] specimens, [[biopsy|rectal biopsy]] specimens or [[liver abscess]] aspirates.''
*There are two culture techniques. They are [[Xenical|xenic]] and [[axenic]] systems.<ref name="pmid12097242">{{cite journal| author=Clark CG, Diamond LS| title=Methods for cultivation of luminal parasitic protists of clinical importance. | journal=Clin Microbiol Rev | year= 2002 | volume= 15 | issue= 3 | pages= 329-41 | pmid=12097242 | doi= | pmc=118080 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=12097242  }} </ref>
*Culture of ''[[Entamoeba|E histolytica]]'' is less sensitive than [[microscopy]] as a detection method.
*Parasite cultures are expensive, labor intensive and difficult to maintain in the diagnostic laboratory.
'''Disadvantage'''
*Culture is not recommended as the routine diagnostic test due to overgrowth of other organisms like [[bacteria]] and [[fungi]] in the [[culture media]].
|-
|-
|Isoenzyme analysis
|[[Isoenzyme]] analysis
|
| colspan="3" |
|
*[[Isoenzyme|Isoenzyme analysis]] is useful in the differentiation of ''[[Entamoeba|Entamoeba species]].<ref name="pmid2889435">{{cite journal| author=Sargeaunt PG, Jackson TF, Wiffen S, Bhojnani R, Williams JE, Felmingham D et al.| title=The reliability of Entamoeba histolytica zymodemes in clinical laboratory diagnosis. | journal=Arch Invest Med (Mex) | year= 1987 | volume= 18 | issue= 2 | pages= 69-75 | pmid=2889435 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=2889435  }} </ref><ref name="pmid1825198">{{cite journal| author=Blanc D, Sargeaunt PG| title=Entamoeba histolytica zymodemes: exhibition of gamma and delta bands only of glucose phosphate isomerase and phosphoglucomutase may be influenced by starch content in the medium. | journal=Exp Parasitol | year= 1991 | volume= 72 | issue= 1 | pages= 87-90 | pmid=1825198 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=1825198  }} </ref><ref name="pmid9033111">{{cite journal| author=Jackson TF, Suparsad S| title=Zymodeme stability of Entamoeba histolytica and E. dispar. | journal=Arch Med Res | year= 1997 | volume= 28 Spec No | issue=  | pages= 304-5 | pmid=9033111 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=9033111  }} </ref>
|
*There are three [[isoenzyme]]s (zymodyme) for ''[[Entamoeba|E histolytica]] and one for [[Entamoeba|E dispar]]''.
*This techniques helps in differentiation of ''[[Entamoeba|E histolytica]]'' and ''[[Entamoeba|E dispar]]'' and is considered [[Gold standard (test)|gold standard]] for diagnosing [[Entamoeba|amoebic]] [[infection]] prior to development of newer DNA-based techniques.
'''Disadvantages'''
*Difficult to perform test, time-consuming procedure, and not always successful.
*The [[isoenzyme]] analysis is negative for many [[microscopy]] positive stool samples.<ref name="pmid8163695">{{cite journal| author=González-Ruiz A, Haque R, Aguirre A, Castañón G, Hall A, Guhl F et al.| title=Value of microscopy in the diagnosis of dysentery associated with invasive Entamoeba histolytica. | journal=J Clin Pathol | year= 1994 | volume= 47 | issue= 3 | pages= 236-9 | pmid=8163695 | doi= | pmc=501902 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=8163695  }} </ref><ref name="pmid9041357">{{cite journal| author=Haque R, Faruque AS, Hahn P, Lyerly DM, Petri WA| title=Entamoeba histolytica and Entamoeba dispar infection in children in Bangladesh. | journal=J Infect Dis | year= 1997 | volume= 175 | issue= 3 | pages= 734-6 | pmid=9041357 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=9041357  }} </ref><ref name="pmid8567882">{{cite journal| author=Haque R, Neville LM, Hahn P, Petri WA| title=Rapid diagnosis of Entamoeba infection by using Entamoeba and Entamoeba histolytica stool antigen detection kits. | journal=J Clin Microbiol | year= 1995 | volume= 33 | issue= 10 | pages= 2558-61 | pmid=8567882 | doi= | pmc=228528 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=8567882  }} </ref><ref name="pmid2894495">{{cite journal| author=Strachan WD, Chiodini PL, Spice WM, Moody AH, Ackers JP| title=Immunological differentiation of pathogenic and non-pathogenic isolates of Entamoeba histolytica. | journal=Lancet | year= 1988 | volume= 1 | issue= 8585 | pages= 561-3 | pmid=2894495 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=2894495  }} </ref>
|-
|-
|Antibody Detection Tests
|[[Antibody]] Detection Tests
|
| colspan="3" |
|
*[[Antibody]] detection tests are useful in the case of [[amoebic liver abscess]] as patients do not have detectable [[parasites]] in [[fece]]s.
|
*The [[sensitivity]] of the test is 100% in patients with [[amoebic liver abscess]]. The techniques include [[ELISA|enzyme-linked immunosorbent assay (ELISA)]], [[Hemagglutination assay|indirect hemagglutination (IHA)]], [[latex agglutination test]], [[immunoelectrophoresis]], [[counterimmunoelectrophoresis|counterimmunoelectrophoresis(CIE)]], the amoebic gel diffusion test, [[immunodiffusion]], [[complement fixation]], and [[immunofluorescence assay|indirect immunofluorescence assay (IFA)]].
'''[[ELISA]]'''
*Useful in the diagnosis of asymptomatic and symptomatic amoebiasis after [[feces|fecal]] examination.
*Useful in amoebic liver abscess and in the evaluation of intestinal and extraintestinal infections where [[organisms]] cannot be detected in [[fece]]s but amoebiasis is suspected.<ref name="pmid8565416">{{cite journal| author=Rosenblatt JE, Sloan LM, Bestrom JE| title=Evaluation of an enzyme-linked immunoassay for the detection in serum of antibodies to Entamoeba histolytica. | journal=Diagn Microbiol Infect Dis | year= 1995 | volume= 22 | issue= 3 | pages= 275-8 | pmid=8565416 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=8565416  }} </ref>
*Easy to perform in the clinical laboratory.
*The presence of [[IgM]] antibodies indicates current infection and [[IgG]] antibodies persists for years after ''[[entamoeba histolytica|E histolytica]] infection.<ref name="pmid9749639">{{cite journal| author=Abd-Alla MD, Jackson TG, Ravdin JI| title=Serum [[IgM]] antibody response to the galactose-inhibitable adherence lectin of ''[[Entameoba histolytica]]''. | journal=Am J Trop Med Hyg | year= 1998 | volume= 59 | issue= 3 | pages= 431-4 | pmid=9749639 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=9749639  }} </ref>
*Presence of antilectin [[antibody|antibodies]] are frequently used for the diagnosis of patients with amoebic liver abscess.<ref name="pmid2388003">{{cite journal| author=Ravdin JI, Jackson TF, Petri WA, Murphy CF, Ungar BL, Gathiram V et al.| title=Association of serum antibodies to adherence lectin with invasive amebiasis and asymptomatic infection with pathogenic Entamoeba histolytica. | journal=J Infect Dis | year= 1990 | volume= 162 | issue= 3 | pages= 768-72 | pmid=2388003 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=2388003  }} </ref>
*The sensitivity is 95%. It is a useful test for the diagnostic clinical laboratory as this test does not have cross reaction with other non-Entamoeba histolytica species.<ref name="pmid9738064">{{cite journal| author=Braga LL, Mendonca Y, Paiva CA, Sales A, Cavalcante AL, Mann BJ| title=Seropositivity for and intestinal colonization with Entamoeba histolytica and entamoeba dispar in individuals in northeastern Brazil. | journal=J Clin Microbiol | year= 1998 | volume= 36 | issue= 10 | pages= 3044-5 | pmid=9738064 | doi= | pmc=105108 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=9738064  }} </ref><ref name="pmid14964807">{{cite journal| author=Goncalves ML, da Silva VL, de Andrade CM, Reinhard K, da Rocha GC, Le Bailly M et al.| title=Amoebiasis distribution in the past: first steps using an immunoassay technique. | journal=Trans R Soc Trop Med Hyg | year= 2004 | volume= 98 | issue= 2 | pages= 88-91 | pmid=14964807 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=14964807  }} </ref><ref name="pmid6287685">{{cite journal| author=Grundy MS| title=Preliminary observations using a multi-layer ELISA method for the detection of Entamoeba histolytica trophozoite antigens in stool samples. | journal=Trans R Soc Trop Med Hyg | year= 1982 | volume= 76 | issue= 3 | pages= 396-400 | pmid=6287685 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=6287685  }} </ref><ref name="pmid10864262">{{cite journal| author=Shamsuzzaman SM, Haque R, Hasin SK, Hashiguchi Y| title=Evaluation of indirect fluorescent antibody test and enzyme-linked immunosorbent assay for diagnosis of hepatic amebiasis in Bangladesh. | journal=J Parasitol | year= 2000 | volume= 86 | issue= 3 | pages= 611-5 | pmid=10864262 | doi=10.1645/0022-3395(2000)086[0611:EOIFAT]2.0.CO;2 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=10864262  }} </ref><ref name="pmid14557296">{{cite journal| author=Tanyuksel M, Petri WA| title=Laboratory diagnosis of amebiasis. | journal=Clin Microbiol Rev | year= 2003 | volume= 16 | issue= 4 | pages= 713-29 | pmid=14557296 | doi= | pmc=207118 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=14557296  }} </ref>
|-
|-
|Antigen Detection Tests
|Antigen Detection Tests
|
| colspan="3" |
|
*The antigen detection tests use [[monoclonal antibodies]] against the Gal/GalNAc-specific lectin of [[Entamoeba|E. histolytica]] or against serine-rich antigen of [[Entamoeba|E. histolytica]].
|
*This test is useful in differentiation of disease causing ''[[Entamoeba|E histolytica]] as there are antigenic differences in the [[lectins]] of ''[[Entamoeba|E histolytica]]'' and ''[[Entamoeba|E dispar]]''.
*The test has good [[sensitivity]] and [[specificity]] for the detection of ''[[Entamoeba|E histolytica]] antigen in stool specimens of patients with [[colitis|amoebic colitis]] and asymptomatic intestinal infection.<ref name="pmid9466756">{{cite journal| author=Haque R, Ali IK, Akther S, Petri WA| title=Comparison of PCR, isoenzyme analysis, and antigen detection for diagnosis of Entamoeba histolytica infection. | journal=J Clin Microbiol | year= 1998 | volume= 36 | issue= 2 | pages= 449-52 | pmid=9466756 | doi= | pmc=104557 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=9466756  }} </ref><ref name="pmid9041357">{{cite journal| author=Haque R, Faruque AS, Hahn P, Lyerly DM, Petri WA| title=Entamoeba histolytica and Entamoeba dispar infection in children in Bangladesh. | journal=J Infect Dis | year= 1997 | volume= 175 | issue= 3 | pages= 734-6 | pmid=9041357 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=9041357  }} </ref><ref name="pmid8567882">{{cite journal| author=Haque R, Neville LM, Hahn P, Petri WA| title=Rapid diagnosis of Entamoeba infection by using Entamoeba and Entamoeba histolytica stool antigen detection kits. | journal=J Clin Microbiol | year= 1995 | volume= 33 | issue= 10 | pages= 2558-61 | pmid=8567882 | doi= | pmc=228528 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=8567882  }} </ref>
*[[Antigen]] detection using [[ELISA]] is is both rapid and technically simple to perform. Hence used in developing countries where amoebiasis is most prevalent.
'''Disadvantage'''
*[[Antigen]]s detected are denatured by fixation of the stool sample. Hence the test is limited to frozen or fresh samples.
|-
|-
|Immunochromatographic Assays
|Immunochromatographic Assays
|
| colspan="3" |
|
*The triage parasite panel (TPP) is used for detection of antigens specific for ''[[Entamoeba|E. histolytica]]/''[[Entamoeba|E. dispar]], [[Giardia lamblia]], and [[Cryptosporidium parvum]] simultaneously.<ref name="pmid16624654">{{cite journal| author=Leiva B, Lebbad M, Winiecka-Krusnell J, Altamirano I, Tellez A, Linder E| title=Overdiagnosis of Entamoeba histolytica and Entamoeba dispar in Nicaragua: a microscopic, triage parasite panel and PCR study. | journal=Arch Med Res | year= 2006 | volume= 37 | issue= 4 | pages= 529-34 | pmid=16624654 | doi=10.1016/j.arcmed.2005.10.009 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=16624654  }} </ref><ref name="pmid10449494">{{cite journal| author=Pillai DR, Kain KC| title=Immunochromatographic strip-based detection of Entamoeba histolytica-E. dispar and Giardia lamblia coproantigen. | journal=J Clin Microbiol | year= 1999 | volume= 37 | issue= 9 | pages= 3017-9 | pmid=10449494 | doi= | pmc=85440 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=10449494  }} </ref>
|
*The [[antigens]] specific for these organisms are used by using specific [[antibodies]] and immobilized on a membrane.
*This test is highly [[Sensitivity|sensitive]] and [[Specificity|specific]].
*This test can be performed within 15 min with fresh or frozen, unfixed human fecal specimens.
'''Disadvantage'''
*This test does not differentiate between ''[[Entamoeba|E histolytica]]'' and ''[[Entamoeba|E dispar]]. Hence not a method of choice for the diagnostic laboratory.
*Stool samples are transported to the laboratory as soon as possible as the test is performed on the fresh or fresh-frozen unpreserved [[stool]] samples.<ref name="pmid10970380">{{cite journal| author=Garcia LS, Shimizu RY, Bernard CN| title=Detection of Giardia lamblia, Entamoeba histolytica/Entamoeba dispar, and Cryptosporidium parvum antigens in human fecal specimens using the triage parasite panel enzyme immunoassay. | journal=J Clin Microbiol | year= 2000 | volume= 38 | issue= 9 | pages= 3337-40 | pmid=10970380 | doi= | pmc=87383 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=10970380  }} </ref><ref name="pmid11136793">{{cite journal| author=Sharp SE, Suarez CA, Duran Y, Poppiti RJ| title=Evaluation of the Triage Micro Parasite Panel for detection of Giardia lamblia, Entamoeba histolytica/Entamoeba dispar, and Cryptosporidium parvum in patient stool specimens. | journal=J Clin Microbiol | year= 2001 | volume= 39 | issue= 1 | pages= 332-4 | pmid=11136793 | doi=10.1128/JCM.39.1.332-334.2001 | pmc=87724 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=11136793  }} </ref>
|}
|}
DNA-Based Diagnostic Tests
===DNA-Based Diagnostic Tests===
*These tests are limited to developed countries in research and clinical laboratories.
*[[feces|Fecal]] specimens for [[DNA|DNA analysis]] may be preserved by refrigeration or in a [[formalin]], SAF or PVA fixative. [[Formalin]] preserves [[cysts]], and [[Polyvinyl alcohol|PVA]] and SAF preserves [[trophozoites]] and [[cysts]] in wet mounts.<ref name="pmid10492774">{{cite journal| author=Ramos F, Zurabian R, Morán P, Ramiro M, Gómez A, Clark CG et al.| title=The effect of formalin fixation on the polymerase chain reaction characterization of Entamoeba histolytica. | journal=Trans R Soc Trop Med Hyg | year= 1999 | volume= 93 | issue= 3 | pages= 335-6 | pmid=10492774 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=10492774  }} </ref><ref name="pmid9196177">{{cite journal| author=Troll H, Marti H, Weiss N| title=Simple differential detection of Entamoeba histolytica and Entamoeba dispar in fresh stool specimens by sodium acetate-acetic acid-formalin concentration and PCR. | journal=J Clin Microbiol | year= 1997 | volume= 35 | issue= 7 | pages= 1701-5 | pmid=9196177 | doi= | pmc=229825 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=9196177  }} </ref>
*The sample medium which is used to transport amoebic DNA is [[ethanol]] and the reagent used for the preservation of fecal samples is 10% buffered formalin solution.<ref name=entamoeba>https://www.cdc.gov/dpdx/reference.html Accessed on February 10, 2017</ref>
*The following are the methods used for [[DNA extraction]] from fecal samples.
{| class="wikitable"
{| class="wikitable"
!Laboratory Methods
!Laboratory Methods
Line 67: Line 99:
|Manual Methods
|Manual Methods
|
|
'''QIAamp tissue kit'''
*QIAamp tissue kit spin columns are used for isolation of [[DNA]] using  2% polyvinylpolypyrrolidone and the purification of [[DNA]] from [[microscopy]] positive samples which improve [[sensitivity]] of the [[PCR]]. This is the most widely used method for the [[DNA]] extraction.<ref name="pmid10898137">{{cite journal| author=Verweij JJ, Blotkamp J, Brienen EA, Aguirre A, Polderman AM| title=Differentiation of Entamoeba histolytica and Entamoeba dispar cysts using polymerase chain reaction on DNA isolated from faeces with spin columns. | journal=Eur J Clin Microbiol Infect Dis | year= 2000 | volume= 19 | issue= 5 | pages= 358-61 | pmid=10898137 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=10898137  }} </ref><ref name="pmid11070218">{{cite journal| author=Verweij JJ, van Lieshout L, Blotkamp C, Brienen EA, van Duivenvoorden S, van Esbroeck M et al.| title=Differentiation of Entamoeba histolytica and Entamoeba dispar using PCR-SHELA and comparison of antibody response. | journal=Arch Med Res | year= 2000 | volume= 31 | issue= 4 Suppl | pages= S44-6 | pmid=11070218 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=11070218  }} </ref>
*Other kits which are used for [[DNA extraction]] include the genomic DNA Prep Plus kit and the XTRAX DNA extraction kit.<ref name="pmid10884867">{{cite journal| author=Evangelopoulos A, Spanakos G, Patsoula E, Vakalis N, Legakis N| title=A nested, multiplex, PCR assay for the simultaneous detection and differentiation of Entamoeba histolytica and Entamoeba dispar in faeces. | journal=Ann Trop Med Parasitol | year= 2000 | volume= 94 | issue= 3 | pages= 233-40 | pmid=10884867 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=10884867  }} </ref><ref name="pmid9374591">{{cite journal| author=Myjak P, Kur J, Pietkiewicz H| title=Usefulness of new DNA extraction procedure for PCR technique in species identification of Entamoeba isolates. | journal=Wiad Parazytol | year= 1997 | volume= 43 | issue= 2 | pages= 163-70 | pmid=9374591 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=9374591  }} </ref>
|-
|-
|Automated Methods
|Automated Methods
|
|
'''MagNA Pure LC DNA isolation kit'''
*With this kit genomic [[DNA]] is lysed from organisms in buffer containing guanidine isothiocyanate and the lysed [[DNA]] binds to magnetic glass particles in chaotropic conditions.<ref name="pmid12409353">{{cite journal| author=Wolk DM, Schneider SK, Wengenack NL, Sloan LM, Rosenblatt JE| title=Real-time PCR method for detection of Encephalitozoon intestinalis from stool specimens. | journal=J Clin Microbiol | year= 2002 | volume= 40 | issue= 11 | pages= 3922-8 | pmid=12409353 | doi= | pmc=139654 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=12409353  }} </ref>
*The magnetic particles are washed to remove impurities and unbound substances.
*The washed [[DNA]] is removed from the magnetic particles under the conditions of elevated temperature and low salt concentration.
*This method is used for [[DNA extraction]] from [[microsporidia]] in fecal specimens.
*This method is not routinely used for [[DNA]] extraction.
|-
|-
|Conventional PCR
|Conventional PCR
|
|
*This is the method of choice in developed countries for epidemiological and clinical studies.<ref name="pmid16274714">{{cite journal| author=Calderaro A, Gorrini C, Bommezzadri S, Piccolo G, Dettori G, Chezzi C| title=Entamoeba histolytica and Entamoeba dispar: comparison of two PCR assays for diagnosis in a non-endemic setting. | journal=Trans R Soc Trop Med Hyg | year= 2006 | volume= 100 | issue= 5 | pages= 450-7 | pmid=16274714 | doi=10.1016/j.trstmh.2005.07.015 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=16274714  }} </ref><ref name="pmid16954247">{{cite journal| author=Hamzah Z, Petmitr S, Mungthin M, Leelayoova S, Chavalitshewinkoon-Petmitr P| title=Differential detection of Entamoeba histolytica, Entamoeba dispar, and Entamoeba moshkovskii by a single-round PCR assay. | journal=J Clin Microbiol | year= 2006 | volume= 44 | issue= 9 | pages= 3196-200 | pmid=16954247 | doi=10.1128/JCM.00778-06 | pmc=1594701 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=16954247  }} </ref><ref name="pmid16380331">{{cite journal| author=Haque R, Petri WA| title=Diagnosis of amebiasis in Bangladesh. | journal=Arch Med Res | year= 2006 | volume= 37 | issue= 2 | pages= 273-6 | pmid=16380331 | doi=10.1016/j.arcmed.2005.09.001 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=16380331  }} </ref><ref name="pmid11923344">{{cite journal| author=Zaki M, Meelu P, Sun W, Clark CG| title=Simultaneous differentiation and typing of Entamoeba histolytica and Entamoeba dispar. | journal=J Clin Microbiol | year= 2002 | volume= 40 | issue= 4 | pages= 1271-6 | pmid=11923344 | doi= | pmc=140395 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=11923344  }} </ref>
*This method helps in identifying [[Entamoeba histolytica]] in various clinical specimens like liver abscess aspirate, feces, and tissues.<ref name="pmid14557296">{{cite journal| author=Tanyuksel M, Petri WA| title=Laboratory diagnosis of amebiasis. | journal=Clin Microbiol Rev | year= 2003 | volume= 16 | issue= 4 | pages= 713-29 | pmid=14557296 | doi= | pmc=207118 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=14557296  }} </ref>
*[[Polymerase chain reaction|PCR]] is used for the detection and differentiation of various ''[[Entamoeba|Entamoeba species]]''.
*18SrDNA is used as a target for the differentiation of ''[[Entamoeba|E histolytica]] and ''[[Entamoeba| E dispar]]''.<ref name="pmid1685555">{{cite journal| author=Clark CG, Diamond LS| title=Ribosomal RNA genes of 'pathogenic' and 'nonpathogenic' Entamoeba histolytica are distinct. | journal=Mol Biochem Parasitol | year= 1991 | volume= 49 | issue= 2 | pages= 297-302 | pmid=1685555 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=1685555  }} </ref><ref name="pmid1364099">{{cite journal| author=Clark CG, Diamond LS| title=Differentiation of pathogenic Entamoeba histolytica from other intestinal protozoa by riboprinting. | journal=Arch Med Res | year= 1992 | volume= 23 | issue= 2 | pages= 15-6 | pmid=1364099 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=1364099  }} </ref><ref name="pmid1594290">{{cite journal| author=Cruz-Reyes JA, Spice WM, Rehman T, Gisborne E, Ackers JP| title=Ribosomal DNA sequences in the differentiation of pathogenic and non-pathogenic isolates of Entamoeba histolytica. | journal=Parasitology | year= 1992 | volume= 104 ( Pt 2) | issue=  | pages= 239-46 | pmid=1594290 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=1594290  }} </ref><ref name="pmid1923831">{{cite journal| author=Que X, Reed SL| title=Nucleotide sequence of a small subunit ribosomal RNA (16S-like rRNA) gene from Entamoeba histolytica: differentiation of pathogenic from nonpathogenic isolates. | journal=Nucleic Acids Res | year= 1991 | volume= 19 | issue= 19 | pages= 5438 | pmid=1923831 | doi= | pmc=328914 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=1923831  }} </ref>
*[[PCR]] methods are highly [[sensitivity|sensitive]] and [[specificity|specific]].<ref name="pmid8253158">{{cite journal| author=Clark CG, Diamond LS| title=Entamoeba histolytica: a method for isolate identification. | journal=Exp Parasitol | year= 1993 | volume= 77 | issue= 4 | pages= 450-5 | pmid=8253158 | doi=10.1006/expr.1993.1105 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=8253158  }} </ref><ref name="pmid9109261">{{cite journal| author=Clark CG, Diamond LS| title=Intraspecific variation and phylogenetic relationships in the genus Entamoeba as revealed by riboprinting. | journal=J Eukaryot Microbiol | year= 1997 | volume= 44 | issue= 2 | pages= 142-54 | pmid=9109261 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=9109261  }} </ref><ref name="pmid12474480">{{cite journal| author=Heckendorn F, N'Goran EK, Felger I, Vounatsou P, Yapi A, Oettli A et al.| title=Species-specific field testing of Entamoeba spp. in an area of high endemicity. | journal=Trans R Soc Trop Med Hyg | year= 2002 | volume= 96 | issue= 5 | pages= 521-8 | pmid=12474480 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=12474480  }} </ref><ref name="pmid9196177">{{cite journal| author=Troll H, Marti H, Weiss N| title=Simple differential detection of Entamoeba histolytica and Entamoeba dispar in fresh stool specimens by sodium acetate-acetic acid-formalin concentration and PCR. | journal=J Clin Microbiol | year= 1997 | volume= 35 | issue= 7 | pages= 1701-5 | pmid=9196177 | doi= | pmc=229825 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=9196177  }} </ref><ref name="pmid10898137">{{cite journal| author=Verweij JJ, Blotkamp J, Brienen EA, Aguirre A, Polderman AM| title=Differentiation of Entamoeba histolytica and Entamoeba dispar cysts using polymerase chain reaction on DNA isolated from faeces with spin columns. | journal=Eur J Clin Microbiol Infect Dis | year= 2000 | volume= 19 | issue= 5 | pages= 358-61 | pmid=10898137 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=10898137  }} </ref>
|-
|-
|Real-Time PCR
|Real-Time PCR
|
|
*Real time PCR is used to differentiate ''[[Entamoeba|E histolytica]]'' from ''[[Entamoeba|E dispar]]''.<ref name="pmid12067606">{{cite journal| author=Klein D| title=Quantification using real-time PCR technology: applications and limitations. | journal=Trends Mol Med | year= 2002 | volume= 8 | issue= 6 | pages= 257-60 | pmid=12067606 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=12067606  }} </ref><ref name="pmid12454128">{{cite journal| author=Blessmann J, Buss H, Nu PA, Dinh BT, Ngo QT, Van AL et al.| title=Real-time PCR for detection and differentiation of Entamoeba histolytica and Entamoeba dispar in fecal samples. | journal=J Clin Microbiol | year= 2002 | volume= 40 | issue= 12 | pages= 4413-7 | pmid=12454128 | doi= | pmc=154634 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=12454128  }} </ref>
*This is an expensive procedure compared to [[antigen]] detection tests and fecal microscopy.
*Real-time [[PCR]] is used diagnose [[amoebiasis]] in developed countries in high risk groups such as [[homosexual]]s, travelers, and immigrants from regions from regions where ''[[Entamoeba| Entamoeba histolytica]]'' is endemic.
|-
|-
|Microarray Development
|Microarray Development
|
|
*[[DNA microarray]] method is rapid and [[Sensitivity|sensitive]] and involves four steps. They are extraction of genomic [[DNA]], amplification of targeted [[DNA]], hybridization of labeled [[DNA]] with [[Oligonucleotides|oligonucleotide probes]] immobilized on a [[DNA microarray|microarray]], and data analysis.<ref name="pmid15243091">{{cite journal| author=Wang Z, Vora GJ, Stenger DA| title=Detection and genotyping of Entamoeba histolytica, Entamoeba dispar, Giardia lamblia, and Cryptosporidium parvum by oligonucleotide microarray. | journal=J Clin Microbiol | year= 2004 | volume= 42 | issue= 7 | pages= 3262-71 | pmid=15243091 | doi=10.1128/JCM.42.7.3262-3271.2004 | pmc=446233 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=15243091  }} </ref>
*This method is used to differentiate between ''[[Entamoeba|E histolytica]]'' and ''[[Entamoeba|E dispar]]''.
*Microarray assays at this time are used as research tool and seldom used for the detection and differentiation of ''[[Entamoeba]]''.
|-
|-
|Typing Methods
|Typing Methods
|
|
*The nested [[PCR]] performed on [[DNA]] extracted from [[liver]] and stool samples helps in identifying the [[polymorphism]] exhibited in the SREHP gene. This is used for the genetic differentiation between strains of ''[[Entamoeba|E histolytica]]''  which cause [[intestinal]] or [[liver]] disease.<ref name="pmid11748961">{{cite journal| author=Ayeh-Kumi PF, Ali IM, Lockhart LA, Gilchrist CA, Petri WA, Haque R| title=Entamoeba histolytica: genetic diversity of clinical isolates from Bangladesh as demonstrated by polymorphisms in the serine-rich gene. | journal=Exp Parasitol | year= 2001 | volume= 99 | issue= 2 | pages= 80-8 | pmid=11748961 | doi=10.1006/expr.2001.4652 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=11748961  }} </ref>
*The strain specific gene (SSG), is also used to differentiate various strains of the [[parasite]].<ref name="pmid1890170">{{cite journal| author=Burch DJ, Li E, Reed S, Jackson TF, Stanley SL| title=Isolation of a strain-specific Entamoeba histolytica cDNA clone. | journal=J Clin Microbiol | year= 1991 | volume= 29 | issue= 4 | pages= 696-701 | pmid=1890170 | doi= | pmc=269855 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=1890170  }} </ref><ref name="pmid8253158">{{cite journal| author=Clark CG, Diamond LS| title=Entamoeba histolytica: a method for isolate identification. | journal=Exp Parasitol | year= 1993 | volume= 77 | issue= 4 | pages= 450-5 | pmid=8253158 | doi=10.1006/expr.1993.1105 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=8253158  }} </ref>
*Other DNA markers of ''[[Entamoeba|E histolytica]] include the chitinase gene, as a marker for studying ''[[Entamoeba|E dispar]]''.
<ref name="pmid12409379">{{cite journal| author=Haghighi A, Kobayashi S, Takeuchi T, Masuda G, Nozaki T| title=Remarkable genetic polymorphism among Entamoeba histolytica isolates from a limited geographic area. | journal=J Clin Microbiol | year= 2002 | volume= 40 | issue= 11 | pages= 4081-90 | pmid=12409379 | doi= | pmc=139687 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=12409379  }} </ref><ref name="pmid9106188">{{cite journal| author=de la Vega H, Specht CA, Semino CE, Robbins PW, Eichinger D, Caplivski D et al.| title=Cloning and expression of chitinases of Entamoebae. | journal=Mol Biochem Parasitol | year= 1997 | volume= 85 | issue= 2 | pages= 139-47 | pmid=9106188 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=9106188  }} </ref>
*Other typing methods include [[Microsatellite|microsatellite typing]]<ref name="pmid15777694">{{cite journal| author=Pinheiro SM, Maciel RF, Morais MA, Aca IS, Carvalho LB, Coimbra MR| title=Genetic characterization of Entamoeba dispar isolates in Northeast Brazil. | journal=Acta Trop | year= 2005 | volume= 94 | issue= 1 | pages= 35-40 | pmid=15777694 | doi=10.1016/j.actatropica.2005.01.012 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=15777694  }} </ref><ref name="pmid11230401">{{cite journal| author=Zaki M, Clark CG| title=Isolation and characterization of polymorphic DNA from Entamoeba histolytica. | journal=J Clin Microbiol | year= 2001 | volume= 39 | issue= 3 | pages= 897-905 | pmid=11230401 | doi=10.1128/JCM.39.3.897-905.2001 | pmc=87847 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=11230401  }} </ref> <ref name="pmid11923344">{{cite journal| author=Zaki M, Meelu P, Sun W, Clark CG| title=Simultaneous differentiation and typing of Entamoeba histolytica and Entamoeba dispar. | journal=J Clin Microbiol | year= 2002 | volume= 40 | issue= 4 | pages= 1271-6 | pmid=11923344 | doi= | pmc=140395 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=11923344  }} </ref> and riboprinting.<ref name="pmid9109261">{{cite journal| author=Clark CG, Diamond LS| title=Intraspecific variation and phylogenetic relationships in the genus Entamoeba as revealed by riboprinting. | journal=J Eukaryot Microbiol | year= 1997 | volume= 44 | issue= 2 | pages= 142-54 | pmid=9109261 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=9109261  }} </ref>
|}
|}


==References==
==References==
{{reflist|2}}
{{reflist|2}}
[[Category:Disease]]
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Latest revision as of 20:23, 29 July 2020

Liver abscess Main Page

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1];Associate Editor(s)-in-Chief: Yamuna Kondapally, M.B.B.S[2]

Overview

Other diagnostic studies include microscopic techniques, culture methods, isoenzyme analysis, antibody detection tests, antigen detection tests, immunochromatographic assays and DNA based diagnostic tests.[1][2][3][4][4]

Other Diagnostic Tests

Needle aspiration

Laboratory Method Findings
Microscopy
Wet (Saline) preparation
  • Very insensitive method (<10%) Procedure
  • The sample is a fresh specimen that should be examined within 1 hr of collection
  • The test is positive when RBCs in trophozoites are detected
  • It is not used in patients without acute dysentery as trophozoites will not contain RBCs
Concentration Technique
  • It is helpful in detecting cysts in the stool sample in asymptomatic carriers
Permanently stained smears
Culture Methods

Disadvantage

  • Culture is not recommended as the routine diagnostic test due to overgrowth of other organisms like bacteria and fungi in the culture media.
Isoenzyme analysis

Disadvantages

  • Difficult to perform test, time-consuming procedure, and not always successful.
  • The isoenzyme analysis is negative for many microscopy positive stool samples.[6][14][15][7]
Antibody Detection Tests

ELISA

  • Useful in the diagnosis of asymptomatic and symptomatic amoebiasis after fecal examination.
  • Useful in amoebic liver abscess and in the evaluation of intestinal and extraintestinal infections where organisms cannot be detected in feces but amoebiasis is suspected.[16]
  • Easy to perform in the clinical laboratory.
  • The presence of IgM antibodies indicates current infection and IgG antibodies persists for years after E histolytica infection.[17]
  • Presence of antilectin antibodies are frequently used for the diagnosis of patients with amoebic liver abscess.[18]
  • The sensitivity is 95%. It is a useful test for the diagnostic clinical laboratory as this test does not have cross reaction with other non-Entamoeba histolytica species.[19][20][21][22][2]
Antigen Detection Tests

Disadvantage

  • Antigens detected are denatured by fixation of the stool sample. Hence the test is limited to frozen or fresh samples.
Immunochromatographic Assays

Disadvantage

  • This test does not differentiate between E histolytica and E dispar. Hence not a method of choice for the diagnostic laboratory.
  • Stool samples are transported to the laboratory as soon as possible as the test is performed on the fresh or fresh-frozen unpreserved stool samples.[26][27]

DNA-Based Diagnostic Tests

  • These tests are limited to developed countries in research and clinical laboratories.
  • Fecal specimens for DNA analysis may be preserved by refrigeration or in a formalin, SAF or PVA fixative. Formalin preserves cysts, and PVA and SAF preserves trophozoites and cysts in wet mounts.[28][29]
  • The sample medium which is used to transport amoebic DNA is ethanol and the reagent used for the preservation of fecal samples is 10% buffered formalin solution.[30]
  • The following are the methods used for DNA extraction from fecal samples.
Laboratory Methods Findings
Manual Methods

QIAamp tissue kit

  • QIAamp tissue kit spin columns are used for isolation of DNA using 2% polyvinylpolypyrrolidone and the purification of DNA from microscopy positive samples which improve sensitivity of the PCR. This is the most widely used method for the DNA extraction.[31][32]
  • Other kits which are used for DNA extraction include the genomic DNA Prep Plus kit and the XTRAX DNA extraction kit.[33][34]
Automated Methods

MagNA Pure LC DNA isolation kit

  • With this kit genomic DNA is lysed from organisms in buffer containing guanidine isothiocyanate and the lysed DNA binds to magnetic glass particles in chaotropic conditions.[35]
  • The magnetic particles are washed to remove impurities and unbound substances.
  • The washed DNA is removed from the magnetic particles under the conditions of elevated temperature and low salt concentration.
  • This method is used for DNA extraction from microsporidia in fecal specimens.
  • This method is not routinely used for DNA extraction.
Conventional PCR
Real-Time PCR
Microarray Development
Typing Methods
  • The nested PCR performed on DNA extracted from liver and stool samples helps in identifying the polymorphism exhibited in the SREHP gene. This is used for the genetic differentiation between strains of E histolytica which cause intestinal or liver disease.[50]
  • The strain specific gene (SSG), is also used to differentiate various strains of the parasite.[51][44]
  • Other DNA markers of E histolytica include the chitinase gene, as a marker for studying E dispar.

[52][53]

References

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  2. 2.0 2.1 2.2 2.3 Tanyuksel M, Petri WA (2003). "Laboratory diagnosis of amebiasis". Clin Microbiol Rev. 16 (4): 713–29. PMC 207118. PMID 14557296.
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