Table 1.
Treatment | Calf | Origin | O. ostertagi | C. oncophora | EPG | ||
---|---|---|---|---|---|---|---|
Males | Females | Males | Females | ||||
Before IVM | A1 | TiHo | 2,070 | 3,230 | 6,470 | 5,270 | 750 |
B1 | Gråmunkehöga | 570 | 670 | 9,070 | 13,600 | 1,000 | |
C1 | Kolsta | 900 | 2,900 | 1,930 | 3,070 | 400 | |
After IVM | A2 | TiHo | 0 | 0 | 3,330 | 5,730 | 150 |
A3 | TiHo | 0 | 0 | 130 | 400 | <50 | |
B2 | Gråmunkehöga | 0 | 0 | 6,000 | 6,200 | 50 | |
B3 | Gråmunkehöga | 100 | 0 | 200 | 200 | <50 | |
C2 | Kolsta | 0 | 0 | 600 | 1,600 | <50 | |
C3 | Kolsta | 0 | 0 | 1,000 | 2,000 | <50 |
Calves were previously each inoculated with a mixture of 40,000 L3 of C. oncophora and O. ostertagi, representing isolates with different deworming history. Calves A1, A2 and A3 were inoculated with equal mixtures of laboratory-maintained C. oncophora and O. ostertagi from TiHo, whereas B1, B2, B3, C1, C2 and C3 were inoculated with cattle nematodes from two different farms in Uppland, Sweden, showing phenotypic clinical IVM resistance in previous field trials. Ten worms from each calf were immediately recovered and stored separately at −80 °C for RT-qPCR, and excessive worms were stored at −20 °C for AFLP analysis