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Molecular identification of Hartmannella vermiformis and Vannella persistens from man-made recreational water environments, Tehran, Iran

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Abstract

A survey was conducted on man-made recreational water located in different regions of Tehran, Iran to detect the free-living amoebae present in ponds and fountains of parks and squares. Fifty water samples from 22 municipal districts of Tehran were screened for free-living amoebae and identified by morphological characters and polymerase chain reaction amplification. Amoebae detected were identified as Hartmannella vermiformis (12 %) and Vannella persistens (4 %), which are the first reports of these two amoebas in recreational water environments of Iran. Since, H. vermiformis, which is highly similar to strains serving as hosts for Legionella pneumophila, is a common component of the microbial community in fresh surface water. Although Vannella spp. is not proved to be pathogenic itself, they are capable of harboring pathogenic intracellular organisms. Due to some reports related to pathogenicity of these amoebas, the particular hazard related to these microorganisms should be taken into account in the encounter with drinking and washing in these waters. We recommend control strategies based on physical removal rather than on disinfection to be adopted where necessary.

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References

  • Centeno M, Rivera F, Cerva L, Tsutsumi V, Gallegos E, Calderon A, Ortiz R, Bonilla P, Ramirez E, Suarez G (1996) Hartmannella vermiformis isolated from the cerebrospinal fluid of a young male patient with meningoencephalitis and bronchopneumonia. Arch Med Res 27:579–586

    PubMed  CAS  Google Scholar 

  • Ettinger MR, Webb SR, Harris SA, Mclninch SP, Garman GC, Brown BL (2003) Distribution of free-living amoebae in James River, Virginia, USA. Parasitol Res 89:6–15

    Article  PubMed  Google Scholar 

  • Hofmann R, Michel R, Schmid EN, Muller K-D (1998) Natural infection with microsporidian organisms (KW19) in Vannella spp. (Gymnamoebia) isolated from a domestic tap-water supply. Parasitol Res 84:164–166

    Article  Google Scholar 

  • Inoue T, Asar S, Tahara K, Hayashi K, Kiritoshi A, Shimomura Y (1998) Acanthamoeba keratitis with symbiosis of Hartmannella amoeba. Am J Ophthalmol 125:721–723

    Article  PubMed  CAS  Google Scholar 

  • Khan NA (2006) Acanthamoeba: biology and increasing importance in human health. FEMS Microbiol Rev 30:564–595

    Article  PubMed  Google Scholar 

  • Kinnear FB (2003) Cytopathogenicity of Acanthamoeba, Vahlkampfia and Hartmannella: quantitive and qualitative in vitro studies on keratocytes. J Infect 46:228–237

    Article  PubMed  CAS  Google Scholar 

  • Kong HH, Chung DI (1996) PCR and RFLP variation of conserved region of small subunit ribosomal DNA among Acanthamoeba isolates assigned to either A. castellanii or A. polyphaga. Korean J Parasitol 34:127–134

    Article  PubMed  CAS  Google Scholar 

  • Kuiper MW, Valster RM, Wullings BA, Boonstra H, Smidt H, Kooij DV (2006) Quantitative detection of the free-living amoeba Hartmannella vermiformis in surface water by using real-time PCR. Appl Environ Microbiol 72:750–756

    Article  Google Scholar 

  • Liang SY, Ji DR, Hsia KT, Hung CC, Sheng WH, Hsu BM, Chen JS, Wu MH, Lai CH, Ji DD (2010) Isolation and identification of Acanthamoeba species related to amebic encephalitis and non-pathogenic free-living amoeba species from rice field. J Appl Microbiol 109:1422–1429

    Article  PubMed  CAS  Google Scholar 

  • Maghsood AH, Sissons J, Rezaeian M, Nolder D, Warhurst D, Khan NA (2005) Acanthamoeba genotype T4 from the UK and Iran and isolation of the T2 genotype from clinical isolates. J Med Microbiol 54:755–759

    Article  PubMed  CAS  Google Scholar 

  • Michel R, Hoffman R, Giese A, Muller KD (1995) Untersuchung vondrei Grundwasserwerken auf Vorkommen von Acanthamoeben, Naeglerien und anderen freilebenden Amoben. Acta Hydrochim Hydrobiol 23:202–211

    Article  CAS  Google Scholar 

  • Michel R, Schmid EN, Boker T, Hager DG, Muller KD, Hoffmann R, Sertz HM (2000) Vannella sp. harboring Microsporidia-like organisms isolated from the contact lens and inflamed eye of a female keratitis patient. Parasitol Res 86:514–520

    Article  PubMed  CAS  Google Scholar 

  • Nazar M, Haghighi A, Niyyati M, Eftekhar M, Tahvildar-biderouni F, Taghipour N, Abadi A, Nazemalhosseini Mojarad E, Athari A (2011) Genotyping of Acanthamoeba amoebae isolated from water in recreational areas of Tehran, Iran. J Water Health 9:603–608

    Article  PubMed  CAS  Google Scholar 

  • Niyyati M, Lorenzo-Morales J, Rahimi F, Motevalli-Haghi A, Martín-Navarro CM, Farnia Sh, Valladares B, Rezaeian M (2009) Isolation and genotyping of potentially pathogenic Acanthamoeba strains from dust sources in Iran. Trans R Soc Trop Med Hyg 103:425–427

    Article  PubMed  CAS  Google Scholar 

  • Pernin P, Pélandakis M, Rouby Y, Faure A, Siclet F (1998) Comparative recoveries of Naegleria fowleri amoebae from seeded river water by filtration and centrifugation. Appl Environ Microbiol 64:955–959

    PubMed  CAS  Google Scholar 

  • Pussard M, Pons R (1977) Morphologie de la paroi kystique et taxonomie du genre Acanthamoeba. Protistologica 13:557–598

    Google Scholar 

  • Sambrook J, Russell DW (2001) Molecular cloning: a laboratory manual. Cold Spring Harbor Laboratory, Cold Spring Harbor

    Google Scholar 

  • Scheid P (2007) Mechanism of intrusion of a microspordian-like organism into the nucleus of host amoebae (Vannella sp.) isolated from a keratitis patient. Parasitol Res 101:1097–1102

    Article  PubMed  CAS  Google Scholar 

  • Schuster FL, Visvesvara GS (2004) Free-living amoebae as opportunistic and non-opportunistic pathogens of humans and animals. Int J Parasitol 34:1001–1027

    Article  PubMed  Google Scholar 

  • Smirnov AV, Brown S (2000) First isolation of a cyst-forming Vannella species, from soil—Vannella persistens n. sp. (Gymnamoebia, Vannellidae). Protistology 1:120–123

    Google Scholar 

  • Smirnov AV (2001) Vannella ebro n. sp. (Lobosea, Gymnamoebia), isolated from cyanobacterial mats in Spain. Eur J Parasitol 37:147–153

    Google Scholar 

  • Smirnov AV, Nassonovab ES, Chaoc E, Cavalier-Smith T (2007) Phylogeny, evolution, and taxonomy of vannellid amoebae. Protistology 158:295–324

    Article  CAS  Google Scholar 

  • Stockman LJ, Wright CJ, Visvesvara GS, Fields BS, Beach MJ (2011) Prevalence of Acanthamoeba spp. and other free-living amoebae in household water, Ohio, USA—1990-1992. Parasitol Res 108:621–627

    Article  PubMed  Google Scholar 

  • Tamura K, Peterson D, Peterson N, Stecher G, Nei M, Kumar S (2011) MEGA5: molecular evolutionary genetics analysis using maximum likelihood, evolutionary distance, and maximum parsimony methods. Mol Biol Evol 28:2731–2739

    Article  PubMed  CAS  Google Scholar 

  • Thompson JD, Higgins DG, Gibson TJ (1994) CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, positions-specific gap penalties and weight matrix choice. Nucl Acid Res 22:4673–4680

    Article  CAS  Google Scholar 

  • Tsvetkova N, Schild M, Panaiotov S, Kurdova-Mintcheva R, Gottstein B, Walochnik J, Aspock H, Lucas MS, Muller N (2004) The identification of free-living environmental isolates of amoebae from Bulgaria. Parasitol Res 92:405–413

    Article  PubMed  Google Scholar 

  • Visvesvara GS, Moura H, Schuster FL (2007) Pathogenic and opportunistic free-living amoebae: Acanthamoeba spp., Balamuthia mandrillaris, Naegleria fowleri, and Sappinia diploidea. FEMS Immun Med Microbiol 50:1–26

    Article  CAS  Google Scholar 

  • Weekers PHH, Gast RJ, Fuerst PA, Byers TJ (1994) Sequence variations in small-subunit ribosomal RNAs of Hartmannella vermiformis and their phylogenetic implications. Mol Biol Evol 11:684–690

    PubMed  CAS  Google Scholar 

Download references

Acknowledgments

We acknowledge the support for a Master’s degree from grant no. 12337 to M. Nazar. The authors are indebted to Dr.SJ. Seied-Tabaii, Dr. A. Keshavarz, and Dr. M. Niyati from the Department of Parasitology and Mycology and to M. Bandepour from the Cellular and Molecular Biology Research Center, Shahid Beheshti University of Medical Sciences for their technical assistance and to Dr. Mariano Hernandez, Department of Molecular Biology, University Institute of Tropical Diseases of Canary Islands, University of La Laguna, Tenerife, Spain in acquaintance with MEGA v.5.0 program.

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Correspondence to Mahdieh Nazar.

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Nazar, M., Haghighi, A., Taghipour, N. et al. Molecular identification of Hartmannella vermiformis and Vannella persistens from man-made recreational water environments, Tehran, Iran. Parasitol Res 111, 835–839 (2012). https://doi.org/10.1007/s00436-012-2906-x

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  • DOI: https://doi.org/10.1007/s00436-012-2906-x

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