Campbell E M, Pert C C, Bowman A S
School of Biological Sciences (Zoology), University of Aberdeen, Tillydrone Avenue, Aberdeen AB24 2TZ, UK.
Parasitology. 2009 Jul;136(8):867-74. doi: 10.1017/S0031182009990357. Epub 2009 Jun 3.
Harnessing the full utility of extensive gene sequences recently available for the economically important sea louse, Lepeophtheirus salmonis, requires the adaptation of modern molecular biology approaches to this non-model organism. Using a putative microsomal prostaglandin E synthase type-2 (PGES2) as a candidate gene, we investigated gene-knockdown by double-stranded RNA interference (dsRNAi) in the small free-living and the larger parasitic stages of L. salmonis. dsRNA was administered to nauplius and copepodid stages by immersion for 7 h. Pre-adult and adults received dsRNA by intra-haemocoelic injection. The extent, speed and persistence of the knockdown effects were determined by RT-PCR. LsPGES2 was abundantly expressed in all life stages, including the non-parasitic stages. Administration of dsRNA to nauplius and copepodids by immersion had no effect on mortality rates and moulting through to copepodids was observed. Dramatic knockdown of LsPGES2 was observed within 7 h and persisted for at least 48 h. Injection of dsRNA had no effect on mortality in pre-adults and adults, but knockdown of LsPGES2 was apparent within 24 h, reaching 95% over the 72 h and was persistent for at least 120 h. The methods developed resulted in rapid and persistent knockdown in L. salmonis suitable for studies in the different stadia.
要充分利用最近获得的经济上重要的海虱——鲑居尾孢虫(Lepeophtheirus salmonis)的大量基因序列,需要将现代分子生物学方法应用于这种非模式生物。我们以一种假定的微粒体前列腺素E合酶2型(PGES2)作为候选基因,研究了双链RNA干扰(dsRNAi)在鲑居尾孢虫自由生活的小阶段和较大的寄生阶段的基因敲除情况。通过浸泡7小时将dsRNA施用于无节幼体和桡足幼体阶段。成年前期和成虫通过血腔注射接受dsRNA。通过RT-PCR确定敲除效果的程度、速度和持续性。LsPGES2在包括非寄生阶段在内的所有生命阶段都大量表达。通过浸泡将dsRNA施用于无节幼体和桡足幼体对死亡率没有影响,并且观察到它们蜕皮至桡足幼体。在7小时内观察到LsPGES2显著敲除,并持续至少48小时。注射dsRNA对成年前期和成虫的死亡率没有影响,但LsPGES2的敲除在24小时内明显,在72小时内达到95%,并持续至少120小时。所开发的方法在鲑居尾孢虫中实现了快速且持久的敲除,适用于不同发育阶段的研究。