JP2001247422A - Bacterium for killing larva of fly, agent for killing larva of fly, and method for killing larva of fly - Google Patents
Bacterium for killing larva of fly, agent for killing larva of fly, and method for killing larva of flyInfo
- Publication number
- JP2001247422A JP2001247422A JP2000057112A JP2000057112A JP2001247422A JP 2001247422 A JP2001247422 A JP 2001247422A JP 2000057112 A JP2000057112 A JP 2000057112A JP 2000057112 A JP2000057112 A JP 2000057112A JP 2001247422 A JP2001247422 A JP 2001247422A
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- JP
- Japan
- Prior art keywords
- fly
- killing
- bacillus subtilis
- bacillus
- fly larvae
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、養鶏場、養豚場、
牧場、その他家畜の糞を堆積する場所でハエが発生し、
病原菌の媒介をする等によって、不衛生な昆虫の筆頭に
挙げられるハエ、特にその成虫を撲滅するための、ハエ
幼虫の殺滅菌及びそれを含有する殺滅剤とハエ幼虫の殺
滅方法に関するものである。The present invention relates to a poultry farm, a pig farm,
Flies occur on ranches and other places where livestock dung is deposited,
For sterilization of fly larvae to eradicate flies, especially adult worms, which are the first of the unsanitary insects by transmitting pathogens, etc., and a killing agent containing the same and a method for killing fly larvae It is.
【0002】[0002]
【従来の技術】ハエを撲滅するために化学物質(殺虫剤)
が長年使用されてきた。そのために、ハエの幼虫並びに
成虫に耐性ができて、化学薬品の殺虫効果が薄れてき
た。しかも、最近では化学殺虫剤の使用が人体に与える
悪影響を指摘されることが多くなっている。特に化学物
質過敏症者にとっては極めて問題が大きい。そこで、特
開平6-72819号では放線菌又は放線菌培養物を有効成分
とする殺ハエ剤が提案されている。2. Description of the Related Art Chemical substances (pesticides) to eradicate flies
Have been used for many years. For this reason, the insects have become resistant to fly larvae and adults, and the insecticidal effect of chemicals has been weakened. In addition, recently, the use of chemical pesticides has been often pointed out to have an adverse effect on the human body. This is particularly problematic for those with chemical sensitivity. Therefore, JP-A-6-72819 proposes a fly killing agent containing actinomycetes or an actinomycete culture as an active ingredient.
【0003】[0003]
【発明が解決しようとする課題】放線菌又は放線菌培養
物を用いる例では、放線菌は分類上細菌類に編入されて
いるが、菌体の形態は一般の細菌とは著しく異なり、む
しろカビ類に似ている。繁殖速度は細菌より緩慢であ
る。そこで、ハエを撲滅するために生ごみや食品工場廃
棄物に使用した場合、殺ハエ効果が小さかったり、ハエ
幼虫のさなぎの段階に至るまで効かないので嫌悪感を早
期に避けることができない。また、使用する場所によっ
ては、菌種により人や家畜に放線菌症という病気を起こ
す場合もある。In the case of using an actinomycete or an actinomycete culture, the actinomycete is incorporated into bacteria in classification, but the morphology of the fungus is remarkably different from that of general bacteria. Similar to kind. Reproduction rate is slower than bacteria. Therefore, when used in food waste or food factory waste to eradicate flies, disgust cannot be avoided early because the effect of killing flies is small or it does not work up to the pupal stage of fly larvae. Also, depending on the place of use, actinomycosis may occur in humans and livestock depending on the bacterial species.
【0004】そこで、化学物質(殺虫剤)を用いることな
く、人畜に安全で、しかも、ハエを特に幼虫の段階で効
率よく撲滅することができる細菌を検討した。Therefore, a bacterium which is safe for humans and animals without using a chemical substance (pesticide) and which can efficiently eradicate flies especially at the stage of larva was studied.
【0005】[0005]
【課題を解決するための手段】上記課題を検討した結
果、枯草菌を主菌とするハエ幼虫の殺滅可能な菌を見出
した。この枯草菌はバチルスサブチルス(Bacillus subt
ilis)とバチルスステアロサーモフィルス(Bacillus ste
arothermophilus)又はこれらの混合菌であり、本発明者
が特許微生物寄託センターへ寄託している枯草菌AT−
3株(受託番号FERM P-16073、以下AT−3株と略記)を
構成する。Bacillus subtilis AT−3は発育の至適温
度が37℃で、Bacillus stearothermophilus AT−3株
は至適温度が55℃である。分類学上は2種ともバチルス
(Bacillus)属の細菌である。このような2種の細菌種の
混合により相乗作用をもたらすものと考えられる。これ
によって排除対象とする昆虫は、確認されただけでも少
なくともハエ、ゴキブリ、イエダニ等である。このバチ
ルスサブチルスを含む菌を鶏糞で培養して発酵鶏糞から
なるハエ幼虫の殺滅剤とした。As a result of studying the above-mentioned problems, a bacterium capable of killing fly larvae mainly comprising Bacillus subtilis was found. This Bacillus subtilis is Bacillus subt.
ilis) and Bacillus stearothermophilus (Bacillus ste
arothermophilus) or a mixed bacterium thereof, and the B. subtilis AT-
3 strains (accession number FERM P-16073, hereinafter abbreviated as AT-3 strain). Bacillus subtilis AT-3 has an optimum growth temperature of 37 ° C, and Bacillus stearothermophilus AT-3 has an optimum temperature of 55 ° C. Both taxonomically Bacillus
(Bacillus). It is believed that the mixing of such two bacterial species produces a synergistic effect. As a result, insects to be excluded are at least flies, cockroaches, house dust mites and the like even if they are confirmed. The bacterium containing this Bacillus subtilis was cultured in chicken dung and used as a killer for fly larvae composed of fermented chicken dung.
【0006】ハエ幼虫の殺滅方法は、堆積畜糞に対して
上記バチルスサブチルスを含む菌を散布することを特徴
とする。また、堆積畜糞に対してとバチルスサブチルス
とバチルスステアロサーモフィルスを含む菌を散布し
て、バチルスサブチルスにより低温から常温域でハエの
幼虫を殺すと共に、バチルスステアロサーモフィルスに
より高温域で熱によりハエの幼虫を殺すことを特徴とす
るハエ幼虫の殺滅方法を開発した。[0006] The method of killing fly larvae is characterized by spraying the bacteria containing Bacillus subtilis on the deposited feces. In addition, the bacteria containing Bacillus subtilis and Bacillus stearothermophilus are sprayed on the deposited feces to kill fly larvae at low to normal temperatures with Bacillus subtilis, and at high temperatures with Bacillus stearothermophilus. A method for killing fly larvae, characterized by killing fly larvae by heat, was developed.
【0007】[0007]
【発明の実施の形態】バチルスサブチルス単体の培養 バチルスサブチルスをブレインハートインフィジョンブ
イヨン培地で37℃,72時間培養してバチルスサブチルス
原液とした。これを大量増殖するため下記表1に示す組
成で更に37℃,72時間培養した。DESCRIPTION OF THE PREFERRED EMBODIMENTS Culture of Bacillus subtilis alone Bacillus subtilis was cultured in a brain heart infusion broth at 37 ° C. for 72 hours to obtain a stock solution of Bacillus subtilis. This was further cultured at 37 ° C. for 72 hours with the composition shown in Table 1 below in order to multiply this mass.
【0008】[0008]
【表1】 [Table 1]
【0009】バチルスステアロサモフィルス単体の培養 バチルスステアロサモフィルスをブレインハートインフ
ィジョンブイヨン培地で55℃,48時間培養してバチルス
ステアロサモフィルス原液とした。これを大量増殖する
ため下記表2に示す組成で更に55℃,72時間培養した。Cultivation of Bacillus stearosamophilus alone Bacillus stearosamophilus was cultured in a brain heart infusion broth at 55 ° C. for 48 hours to obtain a stock solution of Bacillus stearosamophilus. This was further cultured at 55 ° C. for 72 hours with the composition shown in Table 2 below in order to propagate it in large quantities.
【0010】[0010]
【表2】 [Table 2]
【0011】バチルスサブチルスとバチルスステアロサ
モフィルスの混合株の調整 生鶏糞7トンにビール酵母30Kgとブドウ糖3Kgを配合し
た混合物に上記バチルスサブチルス原液45Lとバチルス
ステアロサモフィルス原液30Lを加え攪拌機に温風送り
込む装置を備えた48立方メートルの発酵機に投入し、72
時間37〜40℃に保ち、その後55℃で72時間発酵させたの
ち、取り出して製品とした。Preparation of a mixed strain of Bacillus subtilis and Bacillus stearosamophilus A mixture of 7 tons of raw chicken manure and 30 kg of brewer's yeast and 3 kg of glucose was mixed with 45 L of the above stock solution of Bacillus subtilis and 30 L of Bacillus stearosamophilus stock solution and stirred. Into a 48 cubic meter fermenter equipped with
The temperature was maintained at 37 to 40 ° C., and then fermented at 55 ° C. for 72 hours.
【0012】ハエ幼虫の殺滅例3 ハエ幼虫をシャーレに入れ、上記バチルスサブチルス単
体原液及びバチルスステアロサモフィルス原液をそれぞ
れ別個のシャーレ中にハエ幼虫の身体が濡れる程度に散
布した。その結果、バチルスサブチルス単体原液の場合
常温でハエ幼虫が全滅した。バチルスステアロサモフィ
ルス原液では50℃に保った高温でハエ幼虫が全滅した。Killing example 3 of fly larvae A fly larva was placed in a petri dish, and the above-mentioned undiluted solution of Bacillus subtilis alone and undiluted solution of Bacillus stearosamofilus were sprayed in separate Petri dishes to such an extent that the body of the fly larva became wet. As a result, the fly larva was completely annihilated at room temperature in the case of the undiluted solution of Bacillus subtilis. In the stock solution of Bacillus stearosamophilus, fly larvae were completely annihilated at a high temperature maintained at 50 ° C.
【0013】ハエ幼虫の殺滅例4 上記バチルスサブチルスとバチルスステアロサモフィル
スの混合株を堆積した牛糞約1平方メートルにつき約1
〜1.5Kg散布した。この結果、幼虫は死滅した。30日毎
に散布することによってハエの発生を殆ど抑えることが
できた。Example 4 of killing of fly larvae About one square meter of cow dung on which a mixed strain of Bacillus subtilis and Bacillus stearosamofilus was deposited.
~ 1.5Kg was sprayed. As a result, the larva died. By spraying every 30 days, the occurrence of flies could be almost suppressed.
【0014】AT−3株の培養 鶏糞を常温で堆積して約2週間放置したものの頂上へ白
いチーズ状の菌糸の塊を成長させた。これをブイヨンに
より培養器中で37℃,2日間培養した。ブイヨンの組成
は下記表3の通りである。Culture of AT-3 strain Chicken manure was deposited at room temperature and allowed to stand for about 2 weeks, but a white cheese-like mass of hyphae was grown on the top. This was cultured in a culture vessel at 37 ° C. for 2 days using bouillon. The composition of the bouillon is shown in Table 3 below.
【0015】[0015]
【表3】 [Table 3]
【0016】形成したコロニーからブイヨン培養を複数
回繰返した後、以下の試験を行なった。After repeating the cultivation of broth from the formed colonies a plurality of times, the following test was carried out.
【0017】ハエ幼虫の殺滅例1 ハエが最も発生しやすい夏、残飯、魚、野菜その他家庭
ゴミの堆積を行った。少し腐敗が始まった頃にハエが集
まり始めたので、AT−3株培養原液をゴミ50Kg当たり
1L均一に散布した。その結果、ハエが幼虫の段階で死
滅し、成虫の発生がなかった。Killing example 1 of fly larvae In the summer when flies are most likely to occur, leftovers, fish, vegetables and other household waste were deposited. Since flies began to collect when rot started a little, the AT-3 strain stock solution was sprayed uniformly at 1 L per 50 kg of trash. As a result, the fly died at the larval stage, and no adult emerged.
【0018】ハエ幼虫の殺滅例2 本発明者が特許微生物寄託センターへ寄託している枯草
菌AT−3株(受託番号 FERM P-16073) を上記例同様な
培養減液とし、これを堆肥場での堆肥150Kg当たり2L均
一に散布した。その結果、ハエが幼虫の段階で死滅し、
成虫の発生がなかった。Killing Example 2 of Fly Larvae A Bacillus subtilis AT-3 strain (Accession No. FERM P-16073) deposited by the present inventor at the Patent Microorganisms Depositary Center was used as a culture solution similar to the above example, and this was used as a compost. Spread 2L uniformly per 150Kg of compost in the field. As a result, the fly dies at the larval stage,
There was no adult outbreak.
【0019】[0019]
【発明の効果】本発明によって、化学殺虫剤を用いな
い、人畜に安全で、しかも、ハエを効率よく撲滅するこ
とができることとなった。Industrial Applicability According to the present invention, it is possible to safely eliminate human flies and eliminate flies efficiently without using a chemical insecticide.
【0020】人畜並びに環境を清潔にするので、畜産、
養鶏、養豚、肥料製造等の産業の振興と衛生向上に寄与
すること大である。Livestock and livestock,
It is a major contribution to the promotion of industries such as poultry raising, swine raising, and fertilizer production and improvement of hygiene.
Claims (5)
ルスを含む菌からなるハエ幼虫の殺滅剤。An insecticide for fly larvae comprising a bacterium containing Bacillus subtilis, a bacterium belonging to the genus Bacillus.
物寄託センター寄託のAT−3株(受託番号 FERM P-160
73)であるハエ幼虫の殺滅剤。2. A bacterium containing Bacillus subtilis is an AT-3 strain (Accession No. FERM P-160) deposited at the Patent Microorganisms Depositary.
73) is an insecticide for fly larvae.
又は2記載の菌で鶏糞で培養して生成した発酵鶏糞から
なるハエ幼虫の殺滅剤。3. A bacterium containing Bacillus subtilis.
Or an insecticide for fly larvae consisting of fermented chicken dung produced by culturing chicken dung with the fungus of 2 above.
バチルスサブチルスを含む菌を散布することを特徴とす
るハエ幼虫の殺滅方法。4. A method for killing fly larvae, which comprises spraying the bacteria containing Bacillus subtilis according to claim 1 on sediment.
バチルスサブチルスとバチルスステアロサーモフィルス
を含む菌を散布して、バチルスサブチルスにより低温か
ら常温域でハエの幼虫を殺すと共に、バチルスステアロ
サーモフィルスにより高温域で熱によりハエの幼虫を殺
すことを特徴とするハエ幼虫の殺滅方法。5. Spraying the bacteria containing the Bacillus subtilis and Bacillus stearothermophilus according to any one of claims 1 to 3 against the deposited feces, and killing the fly larvae at a low to normal temperature range with the Bacillus subtilis. A method for killing fly larvae, wherein the fly larvae are killed by heat in a high temperature range by using Bacillus stearothermophilus.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2000057112A JP2001247422A (en) | 2000-03-02 | 2000-03-02 | Bacterium for killing larva of fly, agent for killing larva of fly, and method for killing larva of fly |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2000057112A JP2001247422A (en) | 2000-03-02 | 2000-03-02 | Bacterium for killing larva of fly, agent for killing larva of fly, and method for killing larva of fly |
Publications (1)
Publication Number | Publication Date |
---|---|
JP2001247422A true JP2001247422A (en) | 2001-09-11 |
Family
ID=18577962
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2000057112A Pending JP2001247422A (en) | 2000-03-02 | 2000-03-02 | Bacterium for killing larva of fly, agent for killing larva of fly, and method for killing larva of fly |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2001247422A (en) |
-
2000
- 2000-03-02 JP JP2000057112A patent/JP2001247422A/en active Pending
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