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INU-HOTARUI (Scirpus juncoides var. ohwianus)
with GROUP B/2 resistance: (ALS INHIBITORS)
Inhibition of acetolactate synthase ALS (acetohydroxyacid synthase AHAS)

MUTATION: PROLINE 197 to LEUCINE

Inu-hotarui (Scirpus juncoides var. ohwianus) is a monocot plant in the cyperaceae family. A single amino acid substitution from Proline 197 to Leucine has led to resistance to ALS inhibitors as indicated in the table below.

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Inu-hotarui

Chemistry	Example	Resistance
Imidazolinones	Imazethapyr	Susceptible
Pyrimidinylthiobenzoates	Bispyribac-Na	Susceptible
Sulfonylureas	Chlorsulfuron	Resistant > 10 fold
Triazolopyrimidines	Chloransulam-methyl	Not Determined
Sulfonylaminocarbonyltriazolinone	Flucarbazone-Na	Not Determined

NOTES

REFERENCES

Uchino, A., S. Ogata, H. Kohara, S. Yoshida, T. Yoshioka, and H. Watanabe (2007). Molecular basis of diverse responses to acetolactate synthase-inhibiting herbicides in sulfonylurea-resistant biotypes of Schoenoplectus juncoides. Weed Biology and Management , 7 () : 89-96.

Sulfonylurea-resistant biotypes of Schoenoplectus juncoides were collected from Nakafurano, Shiwa, Matsuyama, and Yurihonjyo in Japan. All of the four biotypes showed resistance to bensulfuron-methyl and thifensulfuron-methyl in whole-plant experiments. The growth of the Nakafurano, Shiwa, and Matsuyama biotypes was inhibited by imazaquin-ammonium and bispyribac-sodium, whereas the Yurihonjyo biotype grew normally after treatment with these herbicides. The herbicide concentration required to inhibit the acetolactate synthase (ALS) enzyme by 50% (I50), obtained using in vivo ALS assays, indicated that the four biotypes were > 10-fold more resistant to thifensulfuron-methyl than a susceptible biotype. The Nakafurano, Shiwa, and Matsuyama biotypes exhibited no or little resistance to imazaquin-ammonium, whereas the Yurihonjyo biotype exhibited 6700-fold resistance to the herbicide. The Nakafurano and Shiwa biotypes exhibited no resistance to bispyribac-sodium, but the Matsuyama biotype exhibited 21-fold resistance and the Yurihonjyo biotype exhibited 260-fold resistance to the herbicide. Two S. juncoides ALS genes (ALS1 and ALS2) were isolated and each was found to contain one intron and to encode an ALS protein of 645 amino acids. Sequencing of the ALS genes revealed an amino acid substitution at Pro197 in either encoded protein (ALS1 or ALS2) in the biotypes from Nakafurano (Pro197?Ser197), Shiwa (Pro197?His197), and Matsuyama (Pro197?Leu197). The ALS2 of the biotype from Yurihonjyo was found to contain a Trp574?Leu574 substitution. The relationships between the responses to ALS-inhibiting herbicides and the amino acid substitutions, which are consistent with previous reports in other plants, indicate that the substitutions at Pro197 and Trp574 are the basis of the resistance to sulfonylureas in these S. juncoides biotypes.