| Autor: |
Romão TP; Department of Entomology, Centro de Pesquisas Aggeu Magalhães/Fundação Oswaldo Cruz, Recife-PE, Brazil., de Melo Chalegre KD, Key S, Ayres CF, Fontes de Oliveira CM, de-Melo-Neto OP, Silva-Filha MH |
| Jazyk: |
angličtina |
| Zdroj: |
The FEBS journal [FEBS J] 2006 Apr; Vol. 273 (7), pp. 1556-68. |
| DOI: |
10.1111/j.1742-4658.2006.05177.x |
| Abstrakt: |
The entomopathogen Bacillus sphaericus is an important tool for the vector control of Culex sp., and its effectiveness has been validated in field trials. The appearance of resistance to this bacterium, however, remains a threat to its use, and attempts have been made to understand the resistance mechanisms. Previous work showed that the resistance to B. sphaericus in a Culex quinquefasciatus colony is associated with the absence of the approximately 60-kDa binary toxin receptor in larvae midgut microvilli. Here, the gene encoding the C. quinquefasciatus toxin receptor, Cqm1, was cloned and sequenced from a susceptible colony. The deduced amino-acid sequence confirmed its identity as an alpha-glucosidase, and analysis of the corresponding gene sequence from resistant larvae implicated a 19-nucleotide deletion as the basis for resistance. This deletion changes the ORF and originates a premature stop codon, which prevents the synthesis of the full-length Cqm1. Expression of the truncated protein, however, was not detected when whole larvae extracts were probed with antibodies raised against an N-terminal 45-kDa recombinant fragment of Cqm1. It seems that the premature stop codon directs the mutated cqm1 to the nonsense-mediated decay pathway of mRNA degradation. In-gel assays confirmed that a single alpha-glucosidase protein is missing from the resistant colony. Further in vitro affinity assays showed that the recombinant fragment binds to the toxin, and mapped the binding site to the N-terminus of the receptor. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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