Table 1.
Gene delivery method | Episomal arrays formed? | Relative frequency of spontaneous chromosomal integration | Heritable transgenesis achieved? | Stable transgenic lines derived? | Technical advantages | Technical disadvantages | Key references |
---|---|---|---|---|---|---|---|
Gonadal microinjection | Yes | Low | Yes | Yes | C. elegans methods easily adapted to Strongyloides and Parastrongyloides | Specialized equipment required; learning curve for microinjection technique | Li et al. 2006; Grant et al. 2006a; Junio et al. 2008 |
Microparticle bombardment | Yes | High | ? | No | DNA transfer protocols are rapid and easy. Potential to transfect large numbers of parasites in a single bombardment | Specialized equipment required. Risk of physical damage to bombarded parasites. Selectable co-transformation markers not yet available | Jackstadt et al. 1999; Davis et al. 1999; Higazi et al. 2002; Praitis et al. 2001, 2006 |
Chemical transformation | Unkown | Unknown | Yes | No | DNA transfer is easy | Maximum gene transfer efficiency in Brugia requires administration during larval moulting | Xu et al. 2011 |