Free Standard AU & NZ Shipping For All Book Orders Over $80!
Register      Login
Crop and Pasture Science Crop and Pasture Science Society
Plant sciences, sustainable farming systems and food quality
RESEARCH ARTICLE

Non-target site mechanism of metribuzin tolerance in induced tolerant mutants of narrow-leafed lupin (Lupinus angustifolius L.)

Gang Pan A B , Ping Si A D , Qin Yu C , Jumin Tu B and Stephen Powles C
+ Author Affiliations
- Author Affiliations

A Centre for Legumes in Mediterranean Agriculture (CLIMA), Faculty of Natural and Agricultural Sciences, The University of Western Australia, Crawley, WA 6009, Australia.

B Department of Agronomy, College of Agriculture and Biotechnology, Zhejiang University, Hangzhou, 310029, China.

C Australian Herbicide Resistance Initiative (AHRI), School of Plant Biology, The University of Western Australia, Crawley, WA 6009, Australia.

D Corresponding author. Email: ping.si@uwa.edu.au

Crop and Pasture Science 63(5) 452-458 https://doi.org/10.1071/CP12065
Submitted: 24 February 2012  Accepted: 28 June 2012   Published: 25 July 2012

Abstract

Narrow-leafed lupin (Lupinus angustifolius L.) is an important grain legume crop in Australia. Metribuzin is an important herbicide used to control weeds in lupin crops. This study investigated metribuzin tolerance mechanism in narrow-leafed lupin by comparing two induced mutants (Tanjil-AZ-33 and Tanjil-AZ-55) of higher metribuzin tolerance with the susceptible wild type. Sequencing of the highly conserved region of the chloroplast psbA gene (target site) revealed that the sequences of the wild type and the mutants were identical and therefore metribuzin tolerance is not target site based. Photosynthetic activity was measured and the leaf photosynthesis of the two tolerant mutants was initially inhibited after metribuzin treatment, but recovered within 2.5 days whereas that of the susceptible plants remained inhibited. The photosynthetic measurements confirmed the target site chloroplast was susceptible and the tolerance mechanism is non-target site based. Investigation with known cytochrome P450 monooxygenase inhibitors (omethoate, malathion and phorate) showed that tolerance could be reversed in both mutants, indicating the tolerance mechanism in two tolerant mutants may involve cytochrome P450 enzymes. Interestingly, the inhibitor tridiphane reversed metribuzin tolerance of only one of the two tolerant mutants, indicating diversity in metribuzin tolerance mechanisms in narrow-leafed lupin. These results signify that further investigation of metribuzin metabolism in these plants is warranted. In conclusion, metribuzin tolerance mechanism in lupin mutants is non-target site based, likely involving P450-mediated metribuzin metabolism.

Additional keywords: cytochrome P450 inhibitor, Lupinus angustifolius L., metribuzin tolerance, photosynthesis, psbA gene sequence.


References

Boydston RA, Slife FW (1986) Alteration of atrazine uptake and metabolism by tridiphane in giant foxtail and corn (Zea mays). Weed Science 34, 850–858.

Brown HM, Neighbors SM (1987) Soybean metabolism of chlorimuron-ethyl: physiological basis for soybean selectivity. Pesticide Biochemistry and Physiology 29, 112–120.
Soybean metabolism of chlorimuron-ethyl: physiological basis for soybean selectivity.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaL1cXjtlGnsQ%3D%3D&md5=fbff1de158632c6c6abdcb6f54df6003CAS |

Christianson ML (1991) Fun with mutants: applying genetic methods to problems of weed physiology. Weed Science 39, 489–496.

Christopher JT, Preston C, Powles SB (1994) Malathion antagonized metabolism-based chlorsulfuron resistance in Lolium rigidum. Pesticide Biochemistry and Physiology 49, 172–182.
Malathion antagonized metabolism-based chlorsulfuron resistance in Lolium rigidum.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK2cXlslejsrc%3D&md5=cb5d684405b4b27d2130b4b291010816CAS |

Davis DG, Olson PA, Swanson HR, Frear DS (1991) Metabolism of the herbicide metribuzin by an N-glucosyltransferase from tomato cell cultures. Plant Science 74, 73–80.
Metabolism of the herbicide metribuzin by an N-glucosyltransferase from tomato cell cultures.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK3MXit1entLc%3D&md5=738a45991fe8bb1f9df0d58d3af5e4cfCAS |

Ezra G, Dekker JH, Stephenson GR (1985) Tridiphane as a synergist for herbicides in corn (Zea mays) and Proso millet (Panicum milliaceum). Weed Science 33, 287–290.

Ferhatoglu Y, Avdiushko S, Barrett M (2005) The basis for the safening of clomazone by phorate insecticide in cotton and inhibitors of cytochrome P450s. Pesticide Biochemistry and Physiology 81, 59–70.
The basis for the safening of clomazone by phorate insecticide in cotton and inhibitors of cytochrome P450s.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2cXhtVOitbjL&md5=bcff23bfd7bc95c82b2bf8625bcf6418CAS |

Frear DS, Mansager ER, Swanson HR, Tanaka FS (1983) Metribuzin metabolism in tomato: isolation and identification of N-glucoside conjugates. Pesticide Biochemistry and Physiology 19, 270–281.
Metribuzin metabolism in tomato: isolation and identification of N-glucoside conjugates.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaL3sXktVWkt74%3D&md5=f4ee3d52086b6d4dc374a72cffb09ed7CAS |

Frear DS, Swanson HR, Mansager ER (1985) Alternate pathways of metribuzin metabolism in soybean: formation of N-glucoside and homoglutathione conjugates. Pesticide Biochemistry and Physiology 23, 56–65.
Alternate pathways of metribuzin metabolism in soybean: formation of N-glucoside and homoglutathione conjugates.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaL2MXhtVyjurs%3D&md5=548d8ace592d4d6374f2750c2a80c416CAS |

Gaul SO, Stephenson GR, Solomon KR (1995) Phytotoxic interaction of tridiphane and metribuzin in metribuzin sensitive and tolerant soybean (Glycine max) and tomato (Lycopersicon esculentum). Weed Science 43, 358–364.

Hammond RB (1986) Phytotoxic interactions among phorate, metribuzin, and certain soybean cultivars. Journal of Economic Entomology 79, 1338–1342.

Kleemann SGL, Gill GS (2007) Differential tolerance in wheat (Triticum aestivum L.) genotypes to metribuzin. Australian Journal of Agricultural Research 58, 452–456.
Differential tolerance in wheat (Triticum aestivum L.) genotypes to metribuzin.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXltFyitrk%3D&md5=914efc780b1746da12c8575ad0b9e9b7CAS |

Mengistu LW, Mueller-Warrant GW, Liston A, Barker RE (2000) PsbA mutation (valine219 to isoleucine) in Poa annua resistant to metribuzin and diuron. Pest Management Science 56, 209–217.
PsbA mutation (valine219 to isoleucine) in Poa annua resistant to metribuzin and diuron.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3cXhvFSis70%3D&md5=74b39755dd330dacb525775be9d7115cCAS |

Mengistu LW, Christoffers MJ, Lym RG (2005) A psbA mutation in Kochia scoparia (L) Schrad from railroad rights-of-way with resistance to diuron, tebuthiuron and metribuzin. Pest Management Science 61, 1035–1042.
A psbA mutation in Kochia scoparia (L) Schrad from railroad rights-of-way with resistance to diuron, tebuthiuron and metribuzin.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2MXhtFGmu7zO&md5=ea52fb87df09ed6f37d91cacf9414dc6CAS |

Moreland DE, Novitzky WP, Levi PE (1989) Selective inhibition of cytochrome P450 isozymes by the herbicide synergist tridiphane. Pesticide Biochemistry and Physiology 35, 42–49.
Selective inhibition of cytochrome P450 isozymes by the herbicide synergist tridiphane.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaL1MXmt1Ohs7c%3D&md5=59ae69f5cba95cb0d88c2539fe6b9d49CAS |

Mougin C, Polge N, Scalla R, Cabanne F (1991) Interactions of various agrochemicals with cytochrome P-450-dependent monooxygenases of wheat cells. Pesticide Biochemistry and Physiology 40, 1–11.
Interactions of various agrochemicals with cytochrome P-450-dependent monooxygenases of wheat cells.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK3MXksVChsrk%3D&md5=fc487df2a2a424312cc66014a1801e23CAS |

Oettmeier W (1999) Herbicide resistance and supersensitivity in photosystem II. Cellular and Molecular Life Sciences 55, 1255–1277.
Herbicide resistance and supersensitivity in photosystem II.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK1MXlslOit7o%3D&md5=d7ec857c2883ecc7d238c5777d90c83dCAS |

Park KW, Mallory-Smith CA (2006) PsbA mutation (Asn266 to Thr) in Senecio vulgaris L. confers resistance to several PS II-inhibiting herbicides. Pest Management Science 62, 880–885.
PsbA mutation (Asn266 to Thr) in Senecio vulgaris L. confers resistance to several PS II-inhibiting herbicides.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD28XpsVOlsro%3D&md5=3bfd56efb19cc0e883ee07f732b9f980CAS |

Powles SB, Yu Q (2010) Evolution in action: plants resistant to herbicides. Annual Review of Plant Biology 61, 317–347.
Evolution in action: plants resistant to herbicides.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3cXnslSjsLo%3D&md5=54e3f366a8472130b376be5a76da3182CAS |

Reith ME, Straus NA (1987) Nucleotide sequence of the chloroplast gene responsible for triazine resistance in canola. Theoretical and Applied Genetics 73, 357–363.
Nucleotide sequence of the chloroplast gene responsible for triazine resistance in canola.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaL2sXitVylsbg%3D&md5=d09e9d6c65eedcd808bb5e9805e6d465CAS |

Schwenger-Erger C, Thiemann J, Barz W, Johanningmeier U, Naber D (1993) Metribuzin resistance in photoautotrophic Chenopodium rubrum cell cultures: characterization of double and triple mutations in the psbA gene. FEBS Letters 329, 43–46.
Metribuzin resistance in photoautotrophic Chenopodium rubrum cell cultures: characterization of double and triple mutations in the psbA gene.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK3sXlsFehsrY%3D&md5=c1b7e0e6f46f8da99b534a1d95958f9cCAS |

Schwenger-Erger C, Böhnisch N, Barz W (1999) A new psbA mutation yielding an amino-acid exchange at the lumen-exposed site of the D1 protein. Zeitschrift fur Naturforschung C 54, 909–914.

Shimabukuro RH (1971) Glutathione conjugation: an enzymatic basis for atrazine resistance in corn. Plant Physiology 47, 10–14.
Glutathione conjugation: an enzymatic basis for atrazine resistance in corn.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaE3MXpvVKgsg%3D%3D&md5=e6fca6bfb0223ba950f31a1cda9a5844CAS |

Si P, Sweetingham MW, Buirchell B, Bowran D, Piper T (2006) Genotypic variation on metribuzin tolerance in narrow-leafed lupin (Lupinus angustifolius L.). Australian Journal of Experimental Agriculture 46, 85–91.
Genotypic variation on metribuzin tolerance in narrow-leafed lupin (Lupinus angustifolius L.).Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD28XhtFyqsLw%3D&md5=c5ae4acd758a50fe524886e01936a7e3CAS |

Si P, Buirchell B, Sweetingham MW (2009) Improved metribuzin tolerance in narrow-leafed lupin (Lupinus angustifolius L.) by induced mutation and field selection. Field Crops Research 113, 282–286.
Improved metribuzin tolerance in narrow-leafed lupin (Lupinus angustifolius L.) by induced mutation and field selection.Crossref | GoogleScholarGoogle Scholar |

Si P, Pan G, Sweetingham M (2011) Semi-dominant genes confer additive tolerance to metribuzin in narrow-leafed lupin (Lupinus angustifolius L.) mutants. Euphytica 177, 411–418.
Semi-dominant genes confer additive tolerance to metribuzin in narrow-leafed lupin (Lupinus angustifolius L.) mutants.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3cXhs1Wms7fE&md5=fc5939fefe053c723316a5c5afaf3dd0CAS |

Siminszky B (2006) Plant cytochrome P450-mediated herbicide metabolism. Phytochemistry Reviews 5, 445–458.
Plant cytochrome P450-mediated herbicide metabolism.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXhvVOisLo%3D&md5=562e25ca728d939c20c412a6a92e3a5cCAS |

Simoneaux BJ, Gould TJ (2008) Plant uptake and metabolism of triazine herbicides. In ‘The triazine herbicides, 50 years revolutionizing agriculture’. (Eds HM LeBaron, JE McFarland, OC Burnside) pp. 73–99. (Elsevier Science: Amsterdam)

Vila-Aiub MM, Neve P, Powles SB (2009) Fitness costs associated with evolved herbicide resistance alleles in plants. New Phytologist 184, 751–767.
Fitness costs associated with evolved herbicide resistance alleles in plants.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1MXhsFOls7%2FF&md5=da1e8da938eb494a9e4c19e135889232CAS |

Waldrop DD, Banks PA (1983) Interaction of herbicides with insecticides in soybeans (Glycine max). Weed Science 31, 730–734.

Yuan JS, Tranel PJ, Stewart CN (2006) Non-target-site herbicide resistance: a family business. Trends in Plant Science 12, 7–13.