t250RV1 were designed to amplify an 805 bp cDNA product, at an annealing temperature of 60 C. The chicken lysozyme gene was used to determine relative quantities of contaminating host cDNA. The for ward primer RW3F and reverse primer RW4R were designed to amplify a 280 bp host cDNA prod uct at an annealing temperature of 60 C. Semi quantitative PCR The predicted coding regions of each protease gene were examined for potential primer sites within 1 kb of each other where possible. Primers were designed as detailed in Table 5. PCRs were conducted on cDNA samples from E. tenella merozoites, gametocytes, unsporulated and sporulated oocysts. PCR were optimized to produce cDNA sized pro ducts. Negative controls of no DNA template and host cDNA were run alongside a positive genomic DNA control.

When genomic DNA products were not amplified, a repeat PCR was performed at longer annealing times to produce the often much larger genomic DNA product. A typical PCR was as follows, 1uL of standardized Dacomitinib cDNA sample, 0. 2 uM forward primer, 0. 2 uM reverse primer, 1 �� Accu Prime reaction mix, and AccuPrime Pfx DNA poly merase. Cycling conditions typically involved an initial denaturation at 95 C for 3 min, followed by 25 cycles of denaturation 95 C for 30 s, annealing at Tm 5 for 1 min, extension at 68 C for 1. 5 min. When products were to be sequenced, a final extension at 68 C for 10 min was performed at the end of the PCR reaction. PCRs were per formed at least twice and, generally, three times for each gene product by a different researcher each time.

All amplified products were gel purified using a QIAquickW Gel Extraction Kit according to the manufacturers instructions and sequenced. When cDNA pro ducts were amplified from different parasite stages, these were pooled and used in sequencing reactions. When cDNA products were not obtained, additional primers were designed and used. If a cDNA product was still unable to be amplified with the second primer pair, genomic DNA products were sequenced to confirm primer specificity. Sequences were analysed using DNASTAR Lasergene 9 Core suite. GAM56 processing assay A frozen sample of purified E. tenella gametocytes was resuspended in PBS to a final volume of 500 uL. Glass beads were added to the suspension and vortexed at full speed for three 1 min pulses with a 1 min pause on ice between each pulse.

After three vortex cycles, the sample was centrifuged and the lysate trans ferred to a clean tube. Equal aliquots of the gametocyte extract were immediately added to either 2 uL of 10�� protease inhibitor or PBS. A zero time sample was taken from the PBS control and immediately added to Laemmli sample buffer and frozen. The assay tubes were incubated at 37 C for 2, 4, 6, 8, 10, 12, 16 or 24 h, after which Laemmli sample buffer was added and samples stored at ?20 C for further assessment. SDS PAGE and immunoblotting were carried out as described previously. Briefly, gametocyte assay samples, resuspended in Laemmli sample