Literature DB >> 12902292

Identification and characterization of two subpopulations of Encephalitozoon intestinalis.

Rebecca M Hoffman1, Marilyn M Marshall, David M Polchert, B Helen Jost.   

Abstract

Microsporidia are obligate intracellular protozoa that have been shown to be pathogenic to most living creatures. The development of in vitro cell culture propagation methods has provided researchers with large numbers of spores and facilitated the study of these organisms. Here, we describe heterogeneity within cell culture-propagated Encephalitozoon intestinalis suspensions. Flow cytometer histograms depicting the log side scatter and forward-angle light scatter of spores from nine suspensions produced over 12 months consistently showed two populations differing in size. The suspensions were composed primarily of the smaller-spore subpopulation (76.4% +/- 5.1%). The presence of two subpopulations was confirmed by microscopic examination and image analysis (P < 0.001). Small subpopulation spores were noninfectious in rabbit kidney (RK13) cell culture infectivity assays, while the large spores were infectious when inocula included > or = 25 spores. The small spores stained brilliantly with fluorescein isothiocyanate-conjugated monoclonal antibody against Encephalitozoon genus spore wall antigen, while the large spores stained poorly. There was no difference in staining intensities using commercial (MicroSporFA) and experimental polyclonal antibodies. Vital-dye (DAPI [4',6'-diamidino-2-phenylindole], propidium iodide, or SYTOX Green) staining showed the spores of the small subpopulation to be permeable to all vital dyes tested, while spores of the large subpopulation were not permeable in the absence of ethanol pretreatment. PCR using primers directed to the 16S rRNA or beta-tubulin genes and subsequent sequence analysis confirmed both subpopulations as E. intestinalis. Our data suggest that existing cell culture propagation methods produce two types of spores differing in infectivity, and the presence of these noninfective spores in purified spore suspensions should be considered when designing disinfection and drug treatment studies.

Entities:  

Mesh:

Substances:

Year:  2003        PMID: 12902292      PMCID: PMC169097          DOI: 10.1128/AEM.69.8.4966-4970.2003

Source DB:  PubMed          Journal:  Appl Environ Microbiol        ISSN: 0099-2240            Impact factor:   4.792


  20 in total

1.  Monoclonal antibody enabling the diagnosis of Encephalitozoon intestinalis in fecal specimens: importance of the mode of selection of hybridomas.

Authors:  M Thellier; S Biligui; I Desportes-Livage; I Accoceberry; A Datry
Journal:  J Eukaryot Microbiol       Date:  2001       Impact factor: 3.346

Review 2.  Laboratory identification of the microsporidia.

Authors:  Lynne S Garcia
Journal:  J Clin Microbiol       Date:  2002-06       Impact factor: 5.948

3.  Low- and medium-pressure UV inactivation of microsporidia Encephalitozoon intestinalis.

Authors:  Debra E Huffman; Angela Gennaccaro; Joan B Rose; Bertrand W Dussert
Journal:  Water Res       Date:  2002-07       Impact factor: 11.236

4.  A spore counting method and cell culture model for chlorine disinfection studies of Encephalitozoon syn. Septata intestinalis.

Authors:  D M Wolk; C H Johnson; E W Rice; M M Marshall; K F Grahn; C B Plummer; C R Sterling
Journal:  Appl Environ Microbiol       Date:  2000-04       Impact factor: 4.792

5.  Developmental expression of two spore wall proteins during maturation of the microsporidian Encephalitozoon intestinalis.

Authors:  J R Hayman; S F Hayes; J Amon; T E Nash
Journal:  Infect Immun       Date:  2001-11       Impact factor: 3.441

6.  Chlorine inactivation of spores of Encephalitozoon spp.

Authors:  C H Johnson; M M Marshall; L A DeMaria; J M Moffet; D G Korich
Journal:  Appl Environ Microbiol       Date:  2003-02       Impact factor: 4.792

7.  Flow cytometric analysis of microsporidia belonging to the genus Encephalitozoon.

Authors:  D M Moss; G P Croppo; S Wallace; G S Visvesvara
Journal:  J Clin Microbiol       Date:  1999-02       Impact factor: 5.948

Review 8.  Utility of microsporidian rRNA in diagnosis and phylogeny: a review.

Authors:  L M Weiss; X Zhu; A Cali; H B Tanowitz; M Wittner
Journal:  Folia Parasitol (Praha)       Date:  1994       Impact factor: 2.122

9.  Comparison of UV inactivation of spores of three encephalitozoon species with that of spores of two DNA repair-deficient Bacillus subtilis biodosimetry strains.

Authors:  Marilyn M Marshall; Samuel Hayes; Jackie Moffett; Charles R Sterling; Wayne L Nicholson
Journal:  Appl Environ Microbiol       Date:  2003-01       Impact factor: 4.792

10.  Viability of Cryptosporidium parvum oocysts: correlation of in vitro excystation with inclusion or exclusion of fluorogenic vital dyes.

Authors:  A T Campbell; L J Robertson; H V Smith
Journal:  Appl Environ Microbiol       Date:  1992-11       Impact factor: 4.792

View more
  1 in total

1.  Cytometric approach for detection of Encephalitozoon intestinalis, an emergent agent.

Authors:  Joana Barbosa; Acácio Gonçalves Rodrigues; Cidália Pina-Vaz
Journal:  Clin Vaccine Immunol       Date:  2009-05-13
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.