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Effect of inoculum age and physical parameters on in vitro culture of the entomopathogenic nematode Steinernema feltiae

Published online by Cambridge University Press:  21 November 2016

L.G. Leite ,
D.I. Shapiro-Ilan ,
S. Hazir  and
M.A. Jackson
L.G. Leite*
Affiliation:
Instituto Biologico, APTA, CP 70, Campinas, SP 13001-970, Brazil
D.I. Shapiro-Ilan*
Affiliation:
USDA-ARS, SEFTNRL, Byron, GA 31008, USA
S. Hazir
Affiliation:
Adnan Menderes University, Faculty of Arts and Sciences, Department of Biology, Aydin-Turkey
M.A. Jackson
Affiliation:
USDA-ARS, NCAUR, Peoria, IL, 61604, USA
*
*E-mails: [email protected] and [email protected]
*E-mails: [email protected] and [email protected]
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Abstract

Entomopathogenic nematodes (EPNs) of the families Steinernematidae and Heterorhabditidae have a symbiotic association with bacteria which makes them virulent against insects. EPNs have been mass produced using in vivo and in vitro methods, including both solid and liquid fermentation. This study assessed the effect of nematode inoculum age on the production of Steinernema feltiae in liquid, solid and biphasic processes. Several physical parameters were also assessed: the effect of medium viscosity, flask size and aeration speed on the recovery and yield of infective juveniles (IJs). Inoculum age treatments included inoculum liquid cultures that were 7, 14, 21 and 28 days old. Nematodes from the same inoculum were added to one liquid medium (liquid culture), one solid medium with bacteria previously grown in sponge (solid culture) and a variation of the solid medium (a biphasic culture), in which the bacteria were first grown in liquid and, then, soaked into the sponges, with the purpose of providing a more homogeneous bacterial culture before nematode inoculation. Experiments were conducted in Erlenmeyer flasks. Eight treatments were established involving combinations of three variables: two media (with and without 0.2% agar), two flask sizes (250 and 150 ml) and two agitation speeds (180 and 280 rpm). The study showed increases in nematode yield for liquid cultures, but not for solid or biphasic cultures, with the advance of the inoculum age up to 28 days of growth. Furthermore, the addition of 0.2% agar to the liquid medium and increasing the aeration rate by using larger flasks with higher agitation speed may increase nematode recovery and final yield. The experiments were conducted using shake flasks but the results may also be applicable for bioreactors.

Type
Research Papers
Information
Journal of Helminthology , Volume 91 , Issue 6 , November 2017 , pp. 686 - 695
Creative Commons
This is a work of the U.S. Government and is not subject to copyright protection in the United States.
Copyright
Copyright © Cambridge University Press 2016

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