A cryopreservation procedure for the rumen protozoon Entodinium caudatum: estimation of its viability by fluorescence microscopy.

Abstract:

AIMS:To study the viability of a culture of the rumen protozoon Entodinium caudatum after a cryopreservation procedure by a fluorescence microscopy staining method. METHODS AND RESULTS:Fluorescence method is based on the different colour of cells depending on their membrane integrity. When the temperature effect was studied either by fluorescence or motility, the techniques were correlated (r = 0.727) and their slopes and intercepts were not different (P > 0.05). However, motility showed a higher variation coefficient (0.40 vs 0.12). There were no differences between cooling rates at cryopreservation (1 and 4 degrees C min-1) at 38, 15 or 5 degrees C, nor after thawing. CONCLUSIONS:Fluorescence staining is more accurate than motility for assessing protozoal viability. Viability after thawing was 0.50, and the number of viable cells per 250 microl straw was 320 and 420 for 1 and 4 degrees C min-1. SIGNIFICANCE AND IMPACT OF THE STUDY:This cryopreservation procedure seems to ensure culture recovery for E. caudatum.

journal_name

Lett Appl Microbiol

authors

de la Fuente G,Cebrián JA,Fondevila M

doi

10.1111/j.1472-765x.2003.01464.x

subject

Has Abstract

pub_date

2004-01-01 00:00:00

pages

164-8

issue

2

eissn

0266-8254

issn

1472-765X

pii

1464

journal_volume

38

pub_type

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