Literature DB >> 25765560

Validation of cell-free culture using scanning electron microscopy (SEM) and gene expression studies.

R Yang1, Y Elankumaran1, N Hijjawi2, U Ryan3.   

Abstract

A cell-free culture system for Cryptosporidium parvum was analysed using scanning electron microscopy (SEM) to characterise life cycle stages and compare gene expression in cell-free culture and cell culture using HCT-8 cells. Cryptosporidium parvum samples were harvested at 2 h, 8 h, 14 h, 26 h, 50 h, 74 h, 98 h, 122 h and 170 h, chemically fixed and specimens were observed using a Zeiss 1555 scanning electron microscope. The presence of sporozoites, trophozoites and type I merozoites were identified by SEM. Gene expression in cell culture and cell-free culture was studied using reverse transcriptase quantitative PCR (RT-qPCR) of the sporozoite surface antigen protein (cp15), the glycoprotein 900 (gp900), the Cryptosporidium oocyst wall protein (COWP) and 18S ribosomal RNA (rRNA) genes in both cell free and conventional cell culture. In cell culture, cp15 expression peaked at 74 h, gp900 expression peaked at 74 h and 98 h and COWP expression peaked at 50 h. In cell-free culture, CP15 expression peaked at 98 h, gp900 expression peaked at 74 h and COWP expression peaked at 122 h. The present study is the first to compare gene expression of C. parvum in cell culture and cell-free culture and to characterise life cycle stages of C. parvum in cell-free culture using SEM. Findings from this study showed that gene expression patterns in cell culture and cell-free culture were similar but in cell-free culture, gene expression was delayed for CP15 and COWP in cell free culture compared with the cell culture system and was lower. Although three life cycle stageswere conclusively identified, improvements in SEM methodology should lead to the detection of more life cycle stages.
Copyright © 2015 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  18S rRNA; COWP; Cryptosporidium; RT-qPCR; SEM; cp15; gp900; mRNA expression

Mesh:

Substances:

Year:  2015        PMID: 25765560     DOI: 10.1016/j.exppara.2015.03.002

Source DB:  PubMed          Journal:  Exp Parasitol        ISSN: 0014-4894            Impact factor:   2.011


  4 in total

1.  Quantitative analysis of Cryptosporidium growth in in vitro culture--the impact of parasite density on the success of infection.

Authors:  Anna Paziewska-Harris; Martin Singer; Gerard Schoone; Henk Schallig
Journal:  Parasitol Res       Date:  2015-10-05       Impact factor: 2.289

2.  Glycoproteins and Gal-GalNAc cause Cryptosporidium to switch from an invasive sporozoite to a replicative trophozoite.

Authors:  Adam Edwinson; Giovanni Widmer; John McEvoy
Journal:  Int J Parasitol       Date:  2015-09-30       Impact factor: 3.981

Review 3.  Organoids and Bioengineered Intestinal Models: Potential Solutions to the Cryptosporidium Culturing Dilemma.

Authors:  Samantha Gunasekera; Alireza Zahedi; Mark O'Dea; Brendon King; Paul Monis; Benjamin Thierry; Jillian M Carr; Una Ryan
Journal:  Microorganisms       Date:  2020-05-11

Review 4.  Past and future trends of Cryptosporidium in vitro research.

Authors:  Alexander J Bones; Lyne Jossé; Charlotte More; Christopher N Miller; Martin Michaelis; Anastasios D Tsaousis
Journal:  Exp Parasitol       Date:  2018-12-03       Impact factor: 2.011

  4 in total

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