Tabashnik Bruce E, Biggs Robert W, Higginson Dawn M, Henderson Scottie, Unnithan Devika C, Unnithan Gopalan C, Ellers-Kirk Christa, Sisterson Mark S, Dennehy Timothy J, Carrière Yves, Morin Shai
Department of Entomology, University of Arizona, Tucson, AZ 85721, USA.
J Econ Entomol. 2005 Jun;98(3):635-44. doi: 10.1603/0022-0493-98.3.635.
Two strains of pink bollworm, Pectinophora gossypiella (Saunders), each derived in 1997 from a different field population, were selected for resistance to Bacillus thuringiensis (Bt) toxin Cry1Ac in the laboratory. One strain (MOV97-R) originated from Mohave Valley in western Arizona; the other strain (SAF97-R) was from Safford in eastern Arizona. Relative to a susceptible laboratory strain, Cry1Ac resistance ratios were 1700 for MOV97-R and 520 for SAF97-R. For the two resistant strains, larval survival did not differ between non-Bt cotton and transgenic cotton producing CrylAc. In contrast, larval survival on Bt cotton was 0% for the two unselected parent strains from which the resistant strains were derived. Previously identified resistance (r) alleles of a cadherin gene (BtR) occurred in both resistant strains: r1 and r3 in MOV97-R, and r1 and r2 in SAF97-R. The frequency of individuals carrying two r alleles (rr) was 1.0 in the two resistant strains and 0.02 in each of the two unselected parent strains. Furthermore, in two hybrid strains with a mixture of susceptible (s) and r alleles at the BtR locus, all survivors on Bt cotton had two r alleles. The results show that resistance to Cry1Ac-producing Bt cotton is associated with recessive r alleles at the BtR locus in the strains of pink bollworm tested here. In conjunction with previous results from two other Bt-resistant strains of pink bollworm (APHIS-98R and AZP-R), results reported here identify the cadherin locus as the leading candidate for molecular monitoring of pink bollworm resistance to Bt cotton.
1997年从不同田间种群分离得到的两种棉红铃虫(Pectinophora gossypiella (Saunders))品系,在实验室中被选育出对苏云金芽孢杆菌(Bt)毒素Cry1Ac具有抗性。一个品系(MOV97-R)源自亚利桑那州西部的莫哈韦谷;另一个品系(SAF97-R)来自亚利桑那州东部的萨福德。相对于一个敏感的实验室品系,MOV97-R对Cry1Ac的抗性比率为1700,SAF97-R为520。对于这两个抗性品系,非Bt棉花和产生Cry1Ac的转基因棉花上幼虫的存活率没有差异。相比之下,这两个抗性品系所源自的未选育亲本品系,在Bt棉花上幼虫的存活率为0%。之前鉴定出的一个钙黏蛋白基因(BtR)的抗性(r)等位基因存在于这两个抗性品系中:MOV97-R中有r1和r3,SAF97-R中有r1和r2。在这两个抗性品系中,携带两个r等位基因(rr)的个体频率为1.0,而在两个未选育亲本品系中均为0.02。此外,在BtR位点具有敏感(s)和r等位基因混合物的两个杂交品系中,在Bt棉花上存活的所有个体都有两个r等位基因。结果表明,在这里测试的棉红铃虫品系中,对产生Cry1Ac的Bt棉花的抗性与BtR位点上的隐性r等位基因有关。结合之前另外两个棉红铃虫Bt抗性品系(APHIS-98R和AZP-R)的结果,本文报道的结果确定钙黏蛋白位点是对棉红铃虫对Bt棉花抗性进行分子监测的主要候选位点。