JP7123380B2 - Acaricidal composition - Google Patents
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- JP7123380B2 JP7123380B2 JP2018112461A JP2018112461A JP7123380B2 JP 7123380 B2 JP7123380 B2 JP 7123380B2 JP 2018112461 A JP2018112461 A JP 2018112461A JP 2018112461 A JP2018112461 A JP 2018112461A JP 7123380 B2 JP7123380 B2 JP 7123380B2
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
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Description
この発明は、殺ダニ用組成物、殺ダニ方法及び防ダニ方法に関する。 The present invention relates to an acaricidal composition, acaricidal method and an acaricidal method.
従来、植物の生長に悪影響を与える害虫の駆除、防除に関する組成物や方法は種々検討、提案されている。特許文献1には、殺ダニ能を有するトリコデルマ(Trichoderma)属に属する真菌が提案されている。特許文献2には、白金粒子と白金粒子以外の金属粒子とを含む殺ダニ組成物や、その組成物を使用した防ダニ部材、防ダニ方法が提案されている。
Conventionally, various studies and proposals have been made on compositions and methods for exterminating and controlling insect pests that adversely affect plant growth.
上記の特許文献の他、トリコデルマ属以外の微生物による殺ダニに関する技術が求められている。 In addition to the above-mentioned patent documents, there is a need for techniques related to acaricidal use of microorganisms other than the genus Trichoderma.
ここで、特許文献3には、コリモナス(Collimonas)属に属する細菌を用いた植物病原菌の増殖抑制方法が提案されているが、このコリモナス属に属する細菌が殺ダニに寄与するか否かは確認されていない。
Here,
そこで、この発明は、コリモナス属細菌の新たな用途を提供することを目的とする。 Accordingly, an object of the present invention is to provide a new use of bacteria belonging to the genus Corymonas.
請求項1の発明は、コリモナス(Collimonas)属に属し、受託番号がNITE P-1104の菌株である細菌を含む殺ダニ用組成物である。
The invention of
この発明によれば、コリモナス属細菌の新たな用途を提供することができる。 INDUSTRIAL APPLICABILITY According to the present invention, it is possible to provide new uses for bacteria belonging to the genus Colymonas.
以下、添付図面を参照して、本発明の実施形態の一例を説明する。 An example of an embodiment of the present invention will be described below with reference to the accompanying drawings.
[殺ダニ組成物]
本実施形態の殺ダニ組成物は、コリモナス(Collimonas)属に属する細菌を含む組成物である。この組成物は、紛体、液体、等種々の形態とすることができる。紛体の形態としては、前記コリモナス属に属する細菌を鉱物微細粉に担持させて、これを公知の粉剤、水和剤へ製剤された形態を例示できる。また、液体の形態としては、前記コリモナス属に属する細菌の培養液が公知の液剤へ製剤された形態を例示できる。
[Acaricidal composition]
The acaricidal composition of the present embodiment is a composition containing bacteria belonging to the genus Collimonas. The composition can be in various forms such as powder and liquid. Examples of the form of the powder include a form in which the bacteria belonging to the genus Corymonas are supported on a fine mineral powder, and the powder is formulated into known powders and wettable powders. In addition, examples of the liquid form include a form in which the culture solution of bacteria belonging to the genus Colymonas is formulated into a known liquid preparation.
本実施形態で使用しているコリモナス属に属する細菌は、平成23年6月9日付けで独立行政法人製品評価技術基盤機構特許微生物寄託センター(日本国千葉県木更津市かずさ鎌足2-5-8)に受託番号NITE P-1104として寄託されているコリモナス属細菌D-25株(以下、「D-25株」という)である。D-25株の菌学的性質を表1~表3に示す。
[殺ダニ及び防ダニ試験]
D-25株による殺ダニ及び防ダニ試験を実施例1、実施例2に示す。
[Acaricidal and acaricidal test]
Acaricidal and acaricidal tests with the D-25 strain are shown in Examples 1 and 2.
(コリモナス属細菌の準備)
D-25株を1/10TSBにて5日間振とう培養した。培養後、培養液の生菌数を3点スポットにより測定した。
(Preparation of Corymonas bacterium)
The D-25 strain was cultured with shaking in 1/10 TSB for 5 days. After culturing, the number of viable cells in the culture medium was measured by 3-point spotting.
(ダニの準備)
試験ではハダニ(Tetranychus urticae)(住化テクノサービス(株)より購入)を使用した。ペーパータオルを敷いたプラスチック容器にインゲン(Phaseolus vulgaris)の葉を数枚敷き、インゲンの葉に前記ハダニを移した。その上にインゲンの葉を数枚置き、不織布で蓋をして所定の湿度に保ちながら前記ハダニを飼育した。
(preparing ticks)
Spider mites (Tetranychus urticae) (purchased from Sumika Techno Service Co., Ltd.) were used in the test. A plastic container lined with paper towels was lined with several leaves of bean (Phaseolus vulgaris), and the spider mites were transferred to the bean leaves. Several leaves of green bean were placed on it, covered with a non-woven fabric, and the spider mites were reared while maintaining a predetermined humidity.
水分を含んだペーパータオルを敷いたインセクトブリーディングディッシュを試験に使用する容器とした。試験は下記の2種類の処理区で行った。 An insect breeding dish lined with wet paper towels was used as the container used for the test. The test was conducted in the following two types of treatment plots.
・処理区1.前処理区(pretreat)
試験に使用するインゲンの葉をD-25株の培養液に5秒間浸漬し、その後、前記インゲンの葉をインセクトブリーディングディッシュに移し、溶液を乾燥させた。乾燥後、ハダニを10匹以上/葉となるように前記インゲンの葉に移した。前記ハダニを移した後、24時間ごとに前記ハダニの生存数及び産卵数を測定した。
・
The bean leaves used for the test were immersed in the D-25 strain culture solution for 5 seconds, after which the bean leaves were transferred to an insect bleeding dish and the solution was dried. After drying, spider mites were transferred to the bean leaves at a rate of 10 or more/leaf. The number of surviving spider mites and the number of eggs laid were determined every 24 hours after transfer of the mites.
・処理区2.浸漬区(dipped)
試験に使用するインゲンの葉にハダニを10匹以上/葉となるように移した。前記ハダニを移した後、前記インゲンの葉をD-25株の培養液に5秒間浸漬し、その後、前記インゲンの葉をインセクトブリーディングディッシュに移し、溶液を乾燥させた。乾燥後、24時間ごとに前記ハダニの生存数及び産卵数を測定した。
・
Green bean leaves used for testing were infested with spider mites at a rate of 10 or more/leaf. After transferring the spider mites, the bean leaves were immersed in the D-25 strain culture solution for 5 seconds, after which the bean leaves were transferred to an insect bleeding dish and the solution was allowed to dry. After drying, the number of surviving spider mites and the number of eggs laid were measured every 24 hours.
また、インゲンの葉を蒸留水に浸漬し、その後、前記インゲンの葉をインセクトブリーディングディッシュに移し、ハダニを移した。これをコントロールとした。なお、インゲンの葉からハダニが逃げないように、水分を含んだ脱脂綿でインゲンの葉を囲んだ。 Bean leaves were also immersed in distilled water and then transferred to an insect bleeding dish to transfer spider mites. This was used as a control. In order to prevent spider mites from escaping from the green bean leaves, the green bean leaves were surrounded by absorbent cotton containing moisture.
上記処理区及びコントロールをそれぞれ3セット準備して試験を行った。その結果を図1~図4に示す。 Three sets were prepared for each of the above treated sections and controls, and the test was conducted. The results are shown in FIGS. 1 to 4. FIG.
(蒸留水の処理区について)
図1~図4に示すように、コントロールとして準備した蒸留水の処理区では、96時間経過後においてもハダニの生存率が80%以上であった。産卵数については、96時間経過後合計258個で、全体個数で割ると6個/個体の産卵数が認められた。
(Regarding distilled water treatment area)
As shown in FIGS. 1 to 4, the survival rate of spider mites was 80% or more even after 96 hours in the distilled water treated area prepared as a control. The number of eggs laid was 258 in total after 96 hours, and when divided by the total number of eggs, the number of eggs laid was 6 per individual.
(前処理区について)
図1~図4に示すように、前処理区では、48-72時間の間にハダニの生存率が大きく低下した。その後は横ばいとなり、96時間経過後では生存率が30%となった。産卵数については、96時間経過後合計175個で、全体個数で割ると4.5個/個体の産卵数であった。
ハダニの生存率は、蒸留水の処理区と比べて低い値であったが、産卵数に有意な差は表れなかった。
(Regarding the pretreatment area)
As shown in FIGS. 1 to 4, the survival rate of spider mites was greatly reduced between 48 and 72 hours in the pretreatment plots. After that, it leveled off, and the survival rate was 30% after 96 hours. The number of eggs laid was 175 in total after 96 hours, which was 4.5 eggs/individual when divided by the total number of eggs.
The survival rate of spider mites was lower than that of the distilled water treatment, but no significant difference was observed in the number of eggs laid.
(浸漬区について)
図1~図4に示すように、浸漬区では、48-72時間の間にハダニの生存率が50%を大きく下回る結果となり、96時間経過後では、生存率は12%程度まで低下した。産卵数についても、96時間経過後48個で、全体個数で割ると1.1個/個体の産卵数となり、蒸留水の処理区、前処理区に比べて極めて有意な差が表れた。
(Regarding the immersion area)
As shown in FIGS. 1 to 4, in the immersion plot, the survival rate of spider mites was far below 50% between 48 and 72 hours, and decreased to about 12% after 96 hours. The number of eggs laid was 48 after 96 hours, and when divided by the total number of eggs, the number of eggs laid was 1.1/individual.
実施例1で説明したD-25株の培養液を100倍に希釈した。イチゴ農家が所有するイチゴの葉をランダムに2枚選び、2cm角に切断したものをLeaf-1、Leaf-2として準備した。希釈したD-25株の培養液をそれぞれの葉に散布(2017年7月14日散布)してハダニの生存観察を行った。その結果を図5、図6に示す。 The D-25 strain culture described in Example 1 was diluted 100 times. Two strawberry leaves owned by a strawberry farmer were randomly selected and cut into 2 cm squares to prepare Leaf-1 and Leaf-2. A diluted culture solution of the D-25 strain was sprayed on each leaf (sprayed on July 14, 2017) to observe the survival of spider mites. The results are shown in FIGS. 5 and 6. FIG.
図5、図6に示すように、散布後-48時間の間にハダニの8-9割が死んでいることが確認された。また、成体のハダニは存在せず、幼体のみが確認された。さらに、卵も多くがしぼんでおり、確認された健常な卵は数個であった。 As shown in FIGS. 5 and 6, it was confirmed that 80-90% of spider mites died within 48 hours after spraying. In addition, there were no adult spider mites, and only juveniles were confirmed. Furthermore, many of the eggs were shriveled, and only a few healthy eggs were confirmed.
実施例1、2の実験結果から、コリモナス属細菌が従来公知の植物病原菌の防除能だけでなく、殺ダニ能及び防ダニ能を有することが確認された。 From the experimental results of Examples 1 and 2, it was confirmed that the bacteria of the genus Corymonas have not only the ability to control conventionally known plant pathogenic fungi, but also acaricidal and acaricidal abilities.
したがって、コリモナス属細菌を含む組成物をダニ及び/又はその生息地に対して施せば、殺ダニ効果を得ることができる。また、コリモナス属細菌を含む組成物を用いれば、植物に防ダニ機能を付与させることができる。特に、コリモナス属細菌がD-25株であれば、上記の効果が顕著に表れる。 Therefore, acaricidal effect can be obtained by applying a composition comprising a colimonas bacterium to mites and/or their habitats. In addition, by using a composition containing bacteria of the genus Corymonas, it is possible to impart an anti-mite function to plants. In particular, when the strain of the bacterium belonging to the genus Corymonas is the D-25 strain, the above effects are remarkably exhibited.
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2013038575A1 (en) | 2011-09-15 | 2013-03-21 | 一般社団法人新環境技術評議会 | Method for inhibiting proliferation of plant pathogenic microbe using collimonas bacterium |
| WO2014141362A1 (en) | 2013-03-11 | 2014-09-18 | 一般社団法人 新環境技術評議会 | Novel collimonas bacteria and method for controlling harmful plant pathogen using said bacteria |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2013038575A1 (en) | 2011-09-15 | 2013-03-21 | 一般社団法人新環境技術評議会 | Method for inhibiting proliferation of plant pathogenic microbe using collimonas bacterium |
| WO2014141362A1 (en) | 2013-03-11 | 2014-09-18 | 一般社団法人 新環境技術評議会 | Novel collimonas bacteria and method for controlling harmful plant pathogen using said bacteria |
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