Laboratory Growth and Genetic Manipulation of Eimeria tenella.

Authors:
Pastor-Fernández I, Pegg E, Macdonald SE, Tomley FM, Blake DP, Marugán-Hernández V
In:
Source: Curr Protoc Microbiol
Publication Date: (2019)
Issue: 53(1): e81
Research Area:
Parasitology
Gene Expression
Basic Research
Cells used in publication:
Eimeria Tenella
Species: unicellular
Tissue Origin:
Platform:
4D-Nucleofector® X-Unit
Experiment

Due to the availability of new and improved nucleofection systems, optimal conditions for E. tenella transfection using the AMAXA™ 4D-Nucleofector™ System, the 16-well Nucleocuvette™ Strips, and a range of transfection buffers have been standardised  (Table 2). The combination of P3 buffer and program EO-114 successfully generated transfected sporozoites. Besides, the use of a 16-well strip system provided ideal conditions for screening multiple constructs and transfection conditions at the same  time, using relatively small numbers of parasites.

Abstract

Eimeria is a genus of apicomplexan parasites that contains a large number of species, most of which are absolutely host-specific. Seven species have been recognized to infect chickens. Infection of susceptible chickens results in an intestinal disease called coccidiosis, characterized by mucoid or hemorrhagic enteritis, which is associated with impaired feed conversion or mortality in severe cases. Intensive farming practices have increased the significance of coccidiosis since parasite transmission is favored by high-density housing of large numbers of susceptible chickens. Routine chemoprophylaxis and/or vaccination with live parasite vaccines provides effective control of Eimeria, although the emergence of drug resistance and the relative cost and production capacity of current vaccine lines can prove limiting. As pressure to reduce drug use in livestock production intensifies, novel vaccination strategies are needed. Development of effective protocols supporting genetic complementation of Eimeria species has until recently been hampered by their inability to replicate efficiently in vitro. Now, the availability of such protocols has raised the prospect of generating transgenic parasite lines that function as vaccine vectors to express and deliver heterologous antigens. For example, this technology has the potential to streamline the production of live anticoccidial vaccines through the generation of parasite lines that co-express immunoprotective antigens derived from multiple Eimeria species. In this paper we describe detailed protocols for genetic manipulation, laboratory growth, and in vivo propagation of Eimeria tenella parasites, which will encourage future work from other researchers to expand biological understanding of Eimeria through reverse genetics.