Details

Autor(en) / Beteiligte

• Yang, Xin
• Xie, Wen
• Wang, Shao-li
• Wu, Qing-jun
• Pan, Hui-peng
• Li, Ru-mei
• Yang, Ni-na
• Liu, Bai-ming
• Xu, Bao-yun
• Zhou, Xiaomao
• Zhang, You-jun

Titel

Two cytochrome P450 genes are involved in imidacloprid resistance in field populations of the whitefly, Bemisia tabaci, in China

Ist Teil von

• Pesticide biochemistry and physiology, 2013-11, Vol.107 (3), p.343-350

Ort / Verlag

United States: Elsevier Inc

Erscheinungsjahr

2013

Quelle

MEDLINE

Beschreibungen/Notizen

• •Bemisia tabaci Q has a wider distribution in China and has developed substantial resistance to imidacloprid in China.•The gene of CYP6CM1 is involved in imidacloprid resistance not only in laboratory populations but also in field populations.•A new gene of cytochrome P450 gene, CYP4C64 is associated with imidacloprid resistance in B. tabaci Q. The sweet potato whitefly, Bemisia tabaci (Gennadius) (Hemiptera:Aleyrodidae), is an invasive and damaging pest of field crops worldwide. The neonicotinoid insecticide imidacloprid has been widely used to control this pest. We assessed the species composition (B vs. Q), imidacloprid resistance, and association between imidacloprid resistance and the expression of five P450 genes for 14–17 B. tabaci populations in 12 provinces in China. Fifteen of 17 populations contained only B. tabaci Q, and two populations contained both B and Q. Seven of 17 populations exhibited moderate to high resistance to imidacloprid, and eight populations exhibited low resistance to imidacloprid, compared with the most susceptible field WHHB population. In a study of 14 of the populations, resistance level was correlated with the expression of the P450 genes CYP6CM1 and CYP4C64 but not with the expression of CYP6CX1, CYP6CX4, or CYP6DZ7. This study indicates that B. tabaci Q has a wider distribution in China than previously reported. Resistance to imidacloprid in field populations of B. tabaci is associated with the increased expression of two cytochrome P450 genes (CYP6CM1 and CYP4C64).