Evenhuis Jason P, Welch Tim, Booth Natha
USDA-ARS, National Center for Cool and Cold Water Aquaculture, 11861 Leetown Rd, Kearneysville, West Virginia 25430, USA.
Dis Aquat Organ. 2013 Jul 9;105(1):75-9. doi: 10.3354/dao02610.
Edwardsiella ictaluri is the etiologic agent of enteric septicemia of catfish, which causes substantial losses in catfish aquaculture. To determine pathogen-host interactions, previous studies have used the green fluorescence protein (GFP) gene. Here, the pEI2 plasmid of E. ictaluri isolate I49 was tagged using a Tn10-GFP-kan cassette to create the green fluorescence-expressing derivative I49-gfp. The Tn10-GFP-kan insertion site was mapped by plasmid sequencing to 663 bp upstream of open reading frame 2 and appeared to be at a neutral site in the plasmid. Purification of the pEI2::GFPKan plasmid and mobilization into E. coli resulted in GFP expression. The isolated pEI2::GFPkan plasmid was used to retransform the wild type I49 isolate (ensuring a single Tn10-GFP-kan insertion) and an independent E. ictaluri isolate, S97-73-3. The wild type and the green fluorescent-tagged strains were compared for modulation of pathogenicity in channel catfish Ictalurus punctatus by immersion challenge. A significant reduction in mortalities occurred for the I49GFPkan strain as compared to its isogenic parent, but no difference was observed between the S97-73-3GFPkan strain and the S97-73-3 wild type. This GFP-tagged plasmid will be useful for determining the effects that the pEI2::GFPkan plasmid has on virulence and host-pathogen interactions between E. ictaluri isolates.
鮰爱德华氏菌是鲶鱼肠道败血症的病原体,在鲶鱼养殖中造成重大损失。为了确定病原体与宿主的相互作用,先前的研究使用了绿色荧光蛋白(GFP)基因。在此,使用Tn10-GFP-kan盒对鮰爱德华氏菌分离株I49的pEI2质粒进行标记,以创建绿色荧光表达衍生物I49-gfp。通过质粒测序将Tn10-GFP-kan插入位点定位到开放阅读框2上游663 bp处,该位点似乎位于质粒的中性位点。纯化pEI2::GFPKan质粒并将其转入大肠杆菌后导致GFP表达。分离得到的pEI2::GFPkan质粒用于再次转化野生型I49分离株(确保单个Tn10-GFP-kan插入)和一个独立的鮰爱德华氏菌分离株S97-73-3。通过浸浴攻毒比较野生型和绿色荧光标记菌株在斑点叉尾鮰中的致病性调节情况。与同基因亲本相比,I49GFPkan菌株的死亡率显著降低,但S97-73-3GFPkan菌株与S97-73-3野生型之间未观察到差异。这种GFP标记质粒将有助于确定pEI2::GFPkan质粒对鮰爱德华氏菌分离株毒力及宿主-病原体相互作用的影响。