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Iranian Journal of Public Health logoLink to Iranian Journal of Public Health
. 2012 Sep 1;41(9):10–17.

Molecular Epidemiology of Human Intestinal Amoebas in Iran

H Hooshyar 1,*, P Rostamkhani 1, M Rezaian 2
PMCID: PMC3494209  PMID: 23193500

Abstract

Many microscopic-based epidemiological surveys on the prevalence of human intestinal pathogenic and non-pathogenic protozoa including intestinal amoeba performed in Iran show a high prevalence of human intestinal amoeba in different parts of Iran. Such epidemiological studies on amoebiasis are confusing, mainly due to recently appreciated distinction between the Entamoeba histolytica, E. dispar and E. moshkovskii. Differential diagnosis can be done by some methods such as PCR-based methods, monoclonal antibodies and the analysis of isoenzyme typing, however the molecular study of these protozoa in Iran is low. Based on molecular studies, it seems that E. dispar is predominant species especially in the central and northern areas of Iran and amoebiasis due to E. histolytica is a rare infection in the country. It is suggested that infection with E. moshkovskii may be common among Iranians. Considering the importance of molecular epidemiology of amoeba in Iran and also the current data, the present study reviews the data currently available on the molecular distribution of intestinal human amoeba in Iran.

Keywords: Amoeba, Entamoeba, Molecular epidemiology, Iran

Introduction

Cases of transmissions for over 18 different human intestinal protozoa have been reported in Iran. Reports on some of these protozoa such as Microspora spp, Cyclospora cayetanensis, Sarcocyctis hominis, Balantidium coli and Entameoba moshkovskii are as case reports but others including pathogen and non-pathogenic species are more common and prevalent. Human intestinal amoeba contain many species, eight of which (Entamoeba histolytica, E. dispar, E. moshkovskii, E. polecki, E. coli, E. hartmanni, Iodamoeba butschlii and Endolimax nana) reside in the human intestinal lumen (1). It is well known that E. histolytica is the only pathological species in humans, that causes about 50 million cases of infections with an annual death rate of over 100,000 worldwide (2). The other human intestinal amoeba are considered non-pathogenic and rarely cause intestinal disease in humans (3,4).

Progress in the molecular epidemiology of protozoa infection has been driven by developments in the laboratory techniques, such as PCR and other molecular biological tools. Application of this method to the epidemiology of human intestinal protozoa (e.g. amoeba) revolutionised the knowledge and concept of epidemiology of parasitic infection. Molecular data on the epidemiology of intestinal protozoa, especially pathogenic amoeba, are important for planning the prevention and control programs.

Up to present, many microscopic-based epidemiological studies on the prevalence of human intestinal pathogenic and non-pathogenic protozoa, including intestinal amoeba, have been performed in different parts of the Iran (57). Although several studies (5,79) showed the high prevalence of human intestinal amoeba in different parts of Iran, however only a few molecular studies on these protozoa were performed in Iran. This is important due to the recent appreciation on the distinction between E. histolytica, E. dispar and E. moshkovskii and signifying that making differential diagnosis cannot be done by microscopy-based methods.

This review performed to determine and provide an overview of the present information on the molecular epidemiology of human intestinal amoeba in Iran.

Material and Methods

Manual and electronic searches in international and national databases and journals were conducted to find the relevant data reporting molecular studies on human intestinal amoeba in Iran. Searching were performed through in the international database such as PubMed (www.ncbi.nlm.nih.gov), Scirus (www.scirus.com), ISI Web of Science (www.isiknowledge.com), Scopus (www.scopus.com), EMBASE (www.embase.com), Science Direct(www.sciencedirect.com), and Google Scholar (scholar.google.com). National database searched were including: Iranmedex (www.iranmedex.com), IranDoc (www.irandoc.ac.ir), Magiran (www.magiran.com) and Scientific Information Database (www.sid.ir). The search covered the articles published up to the 2011.

In an attempt to identify all related studies, a combination of relevant keywords and MeSH terms including the names of each human intestinal amoeba e.g. “Entamoeba”, “Intestinal Amoeba” and the following keywords: “Iran”, “Molecular” or “genum” were used in search strategy. The searching strategy in Iranian databases was the English and Persian transcription with key words related to the study.

To maximize the sensitivity of search, references of selected articles were checked. Moreover the manual search was carried out in the soft and/or hard copies of articles published in scientific journals, reports of research projects and post-graduate theses, as well as the abstracts of scientific articles related to this topic presented at scientific congresses by Iranian researchers.

Results

Entamoeba histolytica and Entamoeba dispar

Entamoeba histolytica and E. dispar are two genetically distinct but morphologically identical species. These two species could be differentiated by some methods such as specific DNA probe, PCR-based methods, monoclonal antibodies and analysis of the isoenzyme typing (10). On the basis of biochemical, immunological and genetic data, a formal re-description of E. histolytica was published in 1993 separated this species from the harmless commensal E. dispar (11). E. histolytica is a potentially pathogenic species, while the E. dispar is non-pathogenic one. Hence the differentiation of the two species is important in clinical diagnosis and treatment and also from an epidemiological point of view.

Given the criteria mentioned, the epidemiology of amoebiasis has changed since the separation of E. histolytica and E. dispar species. Nowadays it is accepted that E. dispar is the predominant species and much more common than the E. histolytica worldwide (12). However in some regions (e.g. Japan, Mexico, India, South Africa, some Central and South American, and Asian Pacific countries) local prevalence of E. histolytica is especially more common among the male homosexuals (13).

Identification and use of molecular tools for accurate differential diagnosis of Entamoeba spp. such as E. histolytica, E. dispar and E. moshkovskii displays a satisfactory change in the epidemiology of amoebiasis.

In Iran a number of epidemiological studies have been carried out on E. histolytica/E. dispar complex using the routine microscopy stool examination with no separation between them. A prevalence rate of >1% to 30% for E. histolytica/E. dispar complex was reported in different parts of Iran (5). A preliminary comparative study of 15 isolates of E. histolytica/E. dispar isolated from Hamadan, by PCR technique showed that all the isolates were E. dispar (14). A field study on the distribution of E. histolytica/E. dispar cyst passers in northern, central, and southern Iran showed the prevalence of infection with E histolytica/E. dispar was 0.78%, 3.9% and 4.6% for central, northern and southern part of Iran, respectively. The minimum prevalence rate was 0.6% in Tehran, Yazd and Ardekan (central Iran), while the highest rate (8.3%) was seen in rural areas of Ahwaz (southern Iran).This study showed that ratio of E. histolytica/E. dispar was higher in southern (tropical and subtropical regions) than the other regions (15).

Data on differential diagnosis of E. histolytica and E. dispar by molecular methods in different regions of Iran showed that a total number of 92.1% isolates were E. dispar and the remaining 7.9% were E. histolytica or mixed infection (16). This study demonstrated that E. dispar is the predominant species found among the “cyst passers” in Iran (16). The ratio of infection rate with two species in cyst passer in different areas were as follow: In central area (semi temperate zone) 3.5% of isolate were identified as E. histolytica, 93% of isolate were E. histolytica and 3.5% of individuals were infected by both species.

In northern (temperate region) 5.9% of isolates were E. histolytica and 94.1% of isolates E. dispar. In southern (tropical and subtropical region) 7.4% of isolates were E. histolytica and 88.9% E. dispar. 3.7% of person in this area had a mixed infection with two species (16). In Tehran and Karaj, the two major metropolitan areas of central Iran differential diagnosis of 49 isolates of E. histolytica/E. dispar using PCR-RFLP revealed that 46 (93.9%) of isolates were E. dispar, while only 2 (4.1%) E. histolytica. One person (2%) had a mixed infection (10). Another study on 21 isolates of E. histolytica/E. dispar complex in fresh stool by PCR in Tehran showed that 95.45% of isolates were E. dispar and only one isolate (4.55%) was found to be E. histolytica (17). This finding is similar with previous study in this area.

Similar observation that made by Rezaian and Hooshyar(2006),using PCR-RFLP on 21 isolates of E. histolytica/E. dispar in rural areas of Ahwaz and Hamidieh (south of Iran) showed that 19 samples (90.48%) were positive for E. dispar; one (4.76%) positive for E. histolytica and another sample (4.76%) showed mixed infection(5). A local prevalence study in urban and rural areas of Gonbad City (north of Iran) using PCR method showed that 16 samples isolated were E. dispar and none of them showed the E. histolytica pattern (18). A study by PCR/gel electrophoresis, by Haghighi et al. (2009) on eight microscopical-positive E. histolytica/E. dispar samples in Zahedan identified, six of them as E. dispar whereas E. histolytica was not detected there at all (19). A comparative study of stool antigen detection kit and PCR for the diagnosis of Entamoeba sp. infection in asymptomatic cyst passers from western (Luristan), northwestern (West Azerbaijan), and northeastern (Golestan) part of Iran, showed that all of the 88 samples containing E. histolytica/E. dispar cysts were negative for E. histolytica (20).

All of these studies showed that E. dispar is the predominant species in Iran and amoebiasis due to E. histolytica is a rare infection in Iran (Table 1). Hooshyar et al. (2004) showed that E. dispar is much more frequent than E. histolytica, and also that the E. histolytica/E. dispar ratio is 1:12. Field-based studies in other countries have found the similar ratios: 1:8.5 (Philippines), 1:2.7 and 1:8 (Bangladesh) and 1:46 (Ivory Coast) (16).

Table 1:

Prevalence of E. histolytica and E. dispar In Iran

Method of Diagnosis Year Region of study (Iran) No of cases Prevalence rate (%) Reference Arthurs (No.)
E. his E. dis Mixed
PCR based Methods 2001 Hamadan 15 - 100 - Fallah M et al. (14)
2001 Tehran 8 - 100 - Hooshyar et al. (22)
1999–2001 Different regions of Iran 101 4/9 92/1 3 Hooshyar et al. (16)
Central region 3/5 97 3/5 Hooshyar et al. (16)
Northern region 5/9 94/1 - Hooshyar et al. (16)
Southern region 7/4 88/9 3/7 Hooshyar et al. (16)
1999–2001 Tehran& Karaj 49 4/1 93/9 2 Hooshyar et al. (10)
2003 Ahwaz & Hamidieh 21 4/8 90/5 4/7 Rezaian andHooshyar (5)
2006 Gonbad 16 - 100 - Nazemalhoseini et al. (18)
2006–2007 Tehran 21 4/55 95/45 - Nazemalhoseini et al. (17)
2008 Zahedan 8 - 100 - Haghighi et al. (19)
2004–2008 Tehran, Zahedan, Gonbad 53 3.54 91/37 - Nazemalhosseini et al. (27)
2010 Khorramabad 16 - 93/75 - Kheirandish et al.(28)
2011 Chelgerd 10 90 10 - Pesthechian et al.(21)
Stool antigen detection & PCR 2006 Lurestan, West Azarbayijan and Golestan 88 - 100 - Solaymani-Mohammadi et al.(20)
Zymodem analysis 2001 Tehran 8 - 100 - Hooshyar et al. (23,24)
2002–2005 South Iran 23 26 74 - Sahebani et al. (25)
2006 Tehran and Kazerun 2 - 100 - Haghighi A (29.24)

The only molecular study on amoeba in Iran revealed that E. histolytica was more prevalent than E. dispar is a new study that published by Pestechian et al. (2011).In this study From 655 stool samples in Chelgard City (Chaharmahal and Bakhtisry), 11 E. histolytica/E .dispar observed. By PCR 10 of them were E. histolytica and 1 E. dispar (21). This finding is unlike the previous reported data in other parts of Iran and need to more study in this region.

Isoenzyme electrophoresis in starch gel used to distinguish between the E. histolytica and E. dispar. The chosen isoenzymes were malic enzyme (ME), phosphoglucomutase (PGM), glucose phosphate isomerase (GPI) and hexokinase (HK). A zymodeme is defined as a group of amoeba strains that share the same electrophoretic patterns and mobility for these enzymes (22).

By simultaneous the examination of the characteristic banding pattern of PGM and GPI, it was the possible to classify the amoeba in to one of more than 20 zymodemes (12). Twenty-one out of totally of 23 different zymodemes described from human isolates. Eight zymodems pattern proved to be those of the E. histolytica (zymodems: II, VI, VII, X, XI, XII, XIV and XX), while the rest were belong to E. dispar. Prior to the development of DNA-based techniques, isoenzyme (zymodeme) analysis of cultured amoebae was considered the gold standard for the diagnosis of amoebic infection and differential diagnosis of amoeba species.

Study on zymodems pattern of 8 isolates of E. dispar from Hooshyar et al. (2001) study and two E. dispar isolates from Tehran and Kazeroon (AS2IR and AS16IR) by Haghighi (2006) in Japan showed that all of them were zymodem I (23, 24).

Isoenzyme analysis of 23 isolate of Entamoeba in south of Iran, cultured in Robinson's medium by Sahebani et al. (2002–2005) showed that six samples (26%) were diagnosed as Entamoeba histolytica and 17 samples (74%) as E. dispar. Zymodemes of E. histolytica were II and XIV and, zymodemes of E. dispar were I, XVI, XVII and XVIII (25). Based on these results we suggested that zymodeme I of E. dispar similar to other subtropical countries is the predominant zymodem of E. disar in Iran.

Diagnosis of the extra intestinal amoebiasis is important and is most often made by serological methods or detection of the organism at the time of biopsy or autopsy (4). Molecular methods such as PCR are increasingly useful tools for the diagnosis of extra intestinal amoebiasis and can provide rapid diagnosis. The first case of Entamoeba histolytica encephalitis diagnosed by PCR of the cerebrospinal fluid of an Iranian patient was done by Solaymani-mohammadi et al. (20). The patient who was born in the Sistan-Baluchestan province of the southeastern Iran, immigrated to the United States, and 4 months prior to the presentation of disease had visited Iran for 3 months. Finally the patient was treated successfully with metronidazole(26).

Entamoeba moshkovskii

Entamoeba moshkovskii also is not distinguishable from E. dispar and E. histolytica in its cyst or throphozoite forms. For making differential diagnosis nowadays some PCR based methods are available. This organism is considered primarily a free-living amoeba and has been found to be common in sewage, clean and waste-contaminated water worldwide (12). E. moshkovskii is osmotolerant, can be cultured at room temperature, and is resistant to some antiamoebic drugs (e.g. emetine), all characteristics that distinguish it from E. histolytica and E. dispar(30,31,32). Up to present E. moshkovskii has rarely been shown to infect humans (33), however a recent study reported a high prevalence (21.1%) of E. moshkovskii has been reported in young children from Bangladesh (34). Also E. moshkovskii was recently detected in patients between 31 and 50 years of age presented with gastrointestinal symptoms in Australia (35).

To date, human isolates of this species has been reported from many studies all over the world such as South Africa 13% (36), Australia 24.7% (35), India 1.9%(37). These and other studied showed that, at least in some parts of the world, E. moshkovskii may be a true human parasite. In Iran, a low prevalence of infection with E. moshkovskii of 1.1% was recorded in a healthy person (20). A recent study in Iran reported that out of 3,825 stool samples examined using single-round PCR assay 2(3.5%), 53(91.4%) and 2( 3.5%) were reported positive for E. histolytica, E. dispar and E. moshkovskii, respectively. One person (1.73%) had mixed infection of E. dispar and E. moshkovskii(27). In this study presence of E. moshkovskii was confirmed by sequencing. A latest one study in Iran showed that Out of 16 person infected with E. histolytica/E. dispar/E. moshkovskii cysts by microscopic examination in Khorramabad, single-round PCR showed from sixteen samples that were microscopically positive, 1 (6.25%) was E. moshkovskii, and 15 (93.75%) were E. dispar(28). Considering of this study we suggest that infection with E. moshkovskii may be common among the Iranians. This is an important point in molecular epidemiology of the amoeba in Iran.

Despite using PCR for the detection of E. moshkhovskii in Iran, no attempt was done for its detection by culture methods.

Other intestinal amoeba

Various intestinal amoeba species (e.g. Entamoeba coli, Entamoeba hartmani, Iodamoeba butchlii and Endolimax nana) are frequently found in the stool of human in Iran. A prevalence rate between 1% to >70% was reported in different population around Iran (5, 1, 9). Although these amoebas spp. are considered to be harmless, care should be taken to avoid mistaken diagnosis with E. histolytica, the causative agents of amoebiasis. There is no reliable data on the molecular epidemiology of the nonpathogenic intestinal amoeba in Iran and all surveys previously done were based on the detection of cysts or trophozoites in stools by using light microscopy.

Discussion

Intestinal protozoan infections (e.g. Entamoeba species) are still a public health concern in Iran. There are no comprehensive data on the epidemiology of E. histolytica in Iran especially since the separation of E. histolytica and E. dispar species. The most probable explanation of this condition is due almost to the reliance of all surveys previously done on stool examination by microscopy, not only in Iran, but also in the other parts of the world, because the current epidemiology of amoebiasis is confusing, mainly due to the recently appreciated distinction between the E. histolytica, E. dispar and E. moshkovskii.

A majority of asymptomatic individuals with cysts detected in their stool were actually infected with non-pathogenic E. dispar, Based on molecular study, It seems that E. dispar is the predominant species in Iran and amoebiasis due to E. histolytica is a rare infection in Iran (16, 18, 20), but the definite and true prevalence rate of E. histolytica still has became a matter of speculation. Identification of the true prevalence of E. histolytica infection in the community is very important to predict the clinical burden of ameobiasis. Thus, the future molecular epidemiological study should be done to determine the true prevalence of E. histolytica and E. dispar, especially in the tropical area of Iran. Although previous studies revealed that Zymodemes of E. histolytica were II and XIV and, zymodemes of E. dispar were I, XVI, XVII and XVIII in Iran, subsequent studies suggested that only four zymodems are valuable for isolate typing (Zymodem II, XIV and XIX for E. histolytica and only zymodem I in E. dispar)(12,38,39).The others zymodemes appear to be of bacterial rather than amoebal origin. The remaining zymodemes are due to interaction with bacterial enzymes that present in xenic cultures(40).However zymodems typing have a very important method in recognition of E. dispar as a separate species.

According to the results of the study on E. moshkovskii in Iran we suggest that human infection with this species may be common among Iranians. This may be considered as an important point in the molecular epidemiology of amoeba in Iran.

It has been well established that differential diagnosis of some harmless human amoeba such as E. hartmanni and other intestinal amoeba may be difficult and controversial. So, molecular diagnostic tools can be useful for the accurate diagnosis of infection with these protozoa.

Based on our knowledge of human intestinal protozoa epidemiology, water and waste water has an important role in transmission of amoeba to human, so these amoebas are considered as the waterborne parasites. Investigating the occurrence of Entamoeba species in surface and waste water and also the molecular identification of them in Iran is necessary.

Ethical considerations

Ethical issues (Including plagiarism, Informed Consent, misconduct, data fabrication and/or falsification, double publication and/or submission, redundancy, etc) have been completely observed by the authors.

Acknowledgments

The authors are grateful to all authors who provided the material for this review and also appreciation to Dr Ardjmand A for his helpful suggestion on this manuscript.

The authors declare that there is no conflict of interests.

References

  • 1.Hooshyar H, Rezaian M. Amoebas. Tehran University of Medical Sciences Publication; Tehran: 2011. (In Persian). [Google Scholar]
  • 2.Tengku SA, Norhayati M. Public health and clinical importance of amoebiasis in Malaysia: A review. Trop Biomed. 2011;28(2):194–222. [PubMed] [Google Scholar]
  • 3.Clark CG, Diamond LS. Ribosomal RNA genes of ‘pathogenic’ and ‘nonpathogenic’ Entamoeba histolytica are distinct. Mol Bioch Parasitol. 1991;49:297–302. doi: 10.1016/0166-6851(91)90073-f. [DOI] [PubMed] [Google Scholar]
  • 4.John TD, Petri WA. Markell and voges Medical Parasitology. 9th ed. Sunders, Elsevier; Miissuri: 2006. [Google Scholar]
  • 5.Rezaian M, Hooshyar H. Differential diagnosis of Entamoeba histolytica from Entamoeba dispar and a study on the intestinal parasites in rural areas of Ahwaz and Hamidieh. J Sch Public Health Ins Public Health Res. 2006;4(4):33–38. [Persian]. [Google Scholar]
  • 6.Mohammad K, Zalie MR, Sirous S, Masjedi MR. Intestinal parasites in Iran. Iranian J Publ Health. 1995;24(3–4):9–26. [Google Scholar]
  • 7.Khousheh-Mehri G, Mobedi I, Kia EB, Kaviani A, Ahmadi SA, Mehdi-Miri SR, Yousefi H, Gholami E. Study on the intestinal parasites in mazandaran province (northern of Iran) Iranian J Publ Health. 2009;29(1–4):155–164. [Google Scholar]
  • 8.Bairami Kuzehkanani A, Rezaei S, Babaei Z, Niyyati M, Hashemi SN, Rezaeian M. Enteric Protozoan Parasites in Rural Areas of Bandar-Abbas, Southern Iran: Comparison of Past and Present Situation. Iranian J Publ Health. 2011;40(1):80–85. [PMC free article] [PubMed] [Google Scholar]
  • 9.Rezaiian M, Hooshyar H. The prevalence of intestinal parasitic infection in rural areas of Tonekabon, Iran. Iranian J Publ Health. 1996;25(3–4):47–58. [Google Scholar]
  • 10.Hooshyar H, Rezaian M, Kazemi B. Distribution and differential diagnosis of Entamoeba histolytica from Entamoeba dispar by the PCR-RFLP method in central Iran. Ann Saudi Med. 2003;23(6):363–366. doi: 10.5144/0256-4947.2003.363. [DOI] [PubMed] [Google Scholar]
  • 11.Diamond LS, Clark CG. A re-description of Entamoeba histolytica, Schaudinn 1903, (Emended Walker, 1911) separating it from Entamoeba dispar, Brumpt 1925. J Euka Microbiol. 1993;40:340–344. doi: 10.1111/j.1550-7408.1993.tb04926.x. [DOI] [PubMed] [Google Scholar]
  • 12.Jakson T. Epidemiology. In: Ravdin JI, editor. Amoebiasis. Imperial College press; London: 2000. pp. 52–53. [Google Scholar]
  • 13.Cecilia Ximénez a, Patricia Morán a, Liliana Rojas a, Alicia Valadez a, Alejandro Gómez b. Reassessment of the epidemiology of amebiasis: State of the art. Inf Genetics Evol. 2009;9:1023–1032. doi: 10.1016/j.meegid.2009.06.008. [DOI] [PubMed] [Google Scholar]
  • 14.Fallah M, Haghighi A, Tachibana H. Preliminary comparative study of Entamoeba histolytica and Entamoeba dispar by PCR technique in Iran. Med J Islamic Rep Iran. 2001;14(4):369–372. [Google Scholar]
  • 15.Hooshyar H, Rezaian M, Mahmoodi M, Farnia Sh, Solaymani-Mohammadi Sh. A Field Study of the Distribution of Entamoeba histolytica/E. dispar Cyst Passers in Northern, Central, and Southern Iran. Iranian J Publ Health. 2004;33(2):28–32. [Google Scholar]
  • 16.Hooshyar H, Rezaian M, Kazemi B, Jeddi-Tehrani M, Solaymani-Mohammadi Sh. The distribution of Entamoeba histolytica and Entamoeba dispar in northern, central, and southern Iran. Parasitol Res. 2004;94:96–100. doi: 10.1007/s00436-004-1175-8. [DOI] [PubMed] [Google Scholar]
  • 17.Nazemalhosseini Mojarad E, Nochi Z, Sahebekhtiari N, Rostami Nejad M, Dabiri H, Haghighi A. Characterization of Entamoeba histolytica and Entamoeba dispar in fresh stool by PCR. Gastro Hepath. 2010;3(1):37–41. [Google Scholar]
  • 18.Nazemalhoseini Mojarad E, Haghighi A, Azimi Rad M, Mesgarian F, Rostami Nejad M, Zali MR. Prevalence of Entamoeba histolytica and Entamoeba dispar in Gonbad City, 2006. Iranian J Parasitol. 2007;2(2):48–52. [Google Scholar]
  • 19.Fotedar R, Stark D, Beebe N, Marriott D, Ellis J, Harkness J. Laboratory diagnosis techniques for Entamoeba species. Clin Microbiol Rev. 2007;20(3):511–531. doi: 10.1128/CMR.00004-07. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Haghighi A, Salimi Khorashad A, Nazemalhosseini Mojarad E, Kazemi B, Rostami Nejad M, Rasti S. Frequency of enteric protozoan parasites among patients with gastrointestinal complaints in medical centers of Zahedan, Iran. Trans Royal Soc Trop Med Hyg. 2009;103(5):452–54. doi: 10.1016/j.trstmh.2008.11.004. [DOI] [PubMed] [Google Scholar]
  • 21.Pestehchian N, Nazary M, Haghighi A, Salehi A, Yosefi H. Frequency of Entamoeba histolytica and Entamoeba dispar prevalence among patients with gastrointestinal complaints inchelgerd city, southwest of Iran. J Res Med Sci. 2011;16(11):1436–1440. [PMC free article] [PubMed] [Google Scholar]
  • 22.Solaymani-Mohammadi Sh, Rezaian M, Babaei Z, Rajabpour A, Meamar AR, Pourbabai A, Petri WA. Comparison of a Stool Antigen Detection Kit and PCR for Diagnosis of Entamoeba histolytica and Entamoeba dispar Infections in Asymptomatic Cyst Passers in Iran. J Clin Microbiol. 2006;44(6):2258–2261. doi: 10.1128/JCM.00530-06. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Hooshyar H, Rezaian M, Kazemi B, Haghighi A. Differentiation of Entamoeba histolytica and Entamoeba dispar by PCR-RFLP (Isolate of Tehran, Iran) Yakhteh Med J. 2002;4(13):11–15. [Google Scholar]
  • 24.Haghighi A. Amoeba and Amoebiasis. Armaghanghalam press; Khonsar: 2011. [Google Scholar]
  • 25.Sahebani N, Akhlaghi L, Urmazdi H, Hatam Gh, Motazedian MH. Examination and separation of zymodemes of Entamoeba histolytica and Entamoeba dispar in the south of Iran. Iranian South Med J. 2005;7(2):107–112. [Google Scholar]
  • 26.Solaymani-Mohammadi Sh, Maggie M, Lam J, Zunt R, Petri Entamoeba histolytica encephalitis diagnosed by PCR of cerebrospinal fluid. Trans R Soc Trop Med Hyg. 2007;101(3):311–3. doi: 10.1016/j.trstmh.2006.05.004. [DOI] [PubMed] [Google Scholar]
  • 27.Nazemalhosseini Mojarad E, Nochi Z, Sahebekhtiari N, Rostami Nejad M, Dabirri H, Zali M, Kazemi B, Haghighi A. Discrimination of Entamoeba moshkovskii in patients with gastrointestinal disorders by single rounded PCR. Japanese J Infect Dis. 2010;63:136–138. [PubMed] [Google Scholar]
  • 28.Kheirandish F, Badparva E, Haghighi A, Nazemalhosseini-Mojarad E, Kazemi B. Differential diagnosis of Entamoeba spp. In gastrointestinal disorder patients in Khorramabad, Iran. African J Microbiol Res. 2011;5(18):2863–2866. [Google Scholar]
  • 29.Haghighi A, Rezaeian M. Isolation of Zymodem I of Entamoeba dispar using isoenzyme analysis method in Iran. Iranian J Basic Med Sci. 2006;9(1):19–23. [Google Scholar]
  • 30.Entner N, Most H. Genetics of Entamoeba: characterization of two new parasitic strains that grow at room temperature (and at 37°C) J Protozool. 1965;12:10–3. doi: 10.1111/j.1550-7408.1965.tb01805.x. [DOI] [PubMed] [Google Scholar]
  • 31.Richards CS, Goldman M, Cannon LT. Cultivation of Entamoeba histolytica and Entamoeba histolytica-like strains at reduced temperature and behavior of the amoebae in diluted media. Am J Trop Med Hyg. 1966;5:648–55. doi: 10.4269/ajtmh.1966.15.648. [DOI] [PubMed] [Google Scholar]
  • 32.Clark CG, Diamond LS. The Laredo strain and other Entamoeba histolytica–like amoebae are Entamoeba moshkovskii. Mol Biochem Parasitol. 1991;46:11–8. doi: 10.1016/0166-6851(91)90194-b. [DOI] [PubMed] [Google Scholar]
  • 33.Haque R, Ali IK, Clark CG, Petri WA., Jr A case report of Entamoeba moshkovskii infection in a Bangladeshi child. Parasitol Int. 1998;47:201–202. [Google Scholar]
  • 34.Ali IK, Hossain MB, Roy S, Ayeh-Kumi PF, Petri WA, Jr, Haque R, Clark CG. Entamoeba moshkovskii infections in children, Bangladesh. Emerg Infect Dis. 2003;9:580–584. doi: 10.3201/eid0905.020548. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 35.Fotedar R, Stark D, Beebe N, Marriott D, Ellis J, Harkness J. PCR detection of Entamoeba histolytica, Entamoeba dispar and Entamoeba moshkovskii in stool samples from Sydney, Australia. J Clin Microbiol. 2007;45:1035–1037. doi: 10.1128/JCM.02144-06. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 36.Beck DL Dogan, Maro N, Sam V, Shao NE, Houpt ER. Highprevalence of Entamoeba moshkovskii in a Tanzanian HIV population. Acta Trop. 2008;107:48–49. doi: 10.1016/j.actatropica.2008.03.013. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37.Khainar K, Parija SC, Palaniappan R. Diagnosis of intestinal amoebiasis by using nested polymerase chain reaction-restriction fragment length polymorphism assay. J Gastroenterol. 2007;59:49–58. doi: 10.1007/s00535-007-2080-6. [DOI] [PubMed] [Google Scholar]
  • 38.Razmjoua E, Haghighi A, Rezaiana M, Kobayashi S, Tomoyoshi Nozaki T. Genetic diversity of glucose phosphate isomerase from Entamoeba histolytica. Parasitol Int. 2006;55(4):307–311. doi: 10.1016/j.parint.2006.08.001. [DOI] [PubMed] [Google Scholar]
  • 39.Razmjou E, Rezaian M, Haghighi Á, Kazemi B, Farzami B, Kobayashi S, Nozaki T. Comparison of the Recombinant Glucosephosphate Isomerase from Different Zymodemes of Entamoeba histolytica with Their Natural Counterparts by Isoenzyme Electrophoresis. Iranian J Publ Health. 2005;34(4):35–40. [Google Scholar]
  • 40.Ali IK, Clark CG, Petri WA. Molecular epidemiology of amoebiasis. Infect Genetic Evol. 2008;8:698–707. doi: 10.1016/j.meegid.2008.05.004. [DOI] [PMC free article] [PubMed] [Google Scholar]

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