第五节--昆虫病原原生动物ppt课件.ppt
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1、第五节第五节 原生动物杀虫剂原生动物杀虫剂主要内容主要内容一、昆虫病原原生动物的特性一、昆虫病原原生动物的特性二、昆虫病原原生动物的种类二、昆虫病原原生动物的种类三、昆虫微孢子虫及其应用三、昆虫微孢子虫及其应用一、昆虫病原原生动物的特性一、昆虫病原原生动物的特性原生动物是一类体型最小、构造最简单的动物。原生动物是一类体型最小、构造最简单的动物。一般为单细胞,需用显微镜才能看到。它的细一般为单细胞,需用显微镜才能看到。它的细胞结构与高等动物细胞基本相同,具有细胞膜、胞结构与高等动物细胞基本相同,具有细胞膜、细胞质和一个或数个细胞核,它们是细胞质和一个或数个细胞核,它们是单细胞生单细胞生物物,没有
2、器官分化,然而它们在运动摄食、繁,没有器官分化,然而它们在运动摄食、繁殖和排泄等方面却有与多细胞动物几乎同样的殖和排泄等方面却有与多细胞动物几乎同样的生理机能。生理机能。原生动物的营养方式有三种:植物性营养、动原生动物的营养方式有三种:植物性营养、动物性营养和物性营养和腐生性营养腐生性营养。一、昆虫病原原生动物的特性一、昆虫病原原生动物的特性1. 单细胞真核生物单细胞真核生物2. 细胞内专性寄生物,不能在人工培养基细胞内专性寄生物,不能在人工培养基上生长,通常采用活寄主繁殖。上生长,通常采用活寄主繁殖。3. 侵染:原生动物的感染常发生在寄主幼侵染:原生动物的感染常发生在寄主幼虫期,经口摄入孢子
3、、孢囊或原生动物虫期,经口摄入孢子、孢囊或原生动物的其他发育阶段,也有些种类可附着在的其他发育阶段,也有些种类可附着在寄主卵表面或在卵内传播。寄主卵表面或在卵内传播。生活史生活史4. 病症:在自然情况下可引起慢性病,患病症:在自然情况下可引起慢性病,患病寄主极少表现出明显的病症,仅表现病寄主极少表现出明显的病症,仅表现出行动迟缓、食欲缺乏,生长发育不正出行动迟缓、食欲缺乏,生长发育不正常。在感病过程中,寄主未发育成熟即常。在感病过程中,寄主未发育成熟即死亡。有些种类则能引起细菌败血症,死亡。有些种类则能引起细菌败血症,导致寄主快速死亡。导致寄主快速死亡。二、昆虫病原原生动物的种类二、昆虫病原原
4、生动物的种类及生物学特性及生物学特性有毛根足门有毛根足门真孢子虫门真孢子虫门奇嵌孢虫门奇嵌孢虫门纤毛虫门纤毛虫门微孢子虫门SarcomastigophoraSarcomastigophora有毛根足有毛根足门门 细胞含一细胞核有性生殖为配子生殖运动胞器是鞭毛或伪足或两者皆有ApicomplexaApicomplexa 真孢子虫门真孢子虫门 生活史一定阶段存在顶复合器结构,并在某些阶段存在微孔无纤毛全部寄生AscetosporaAscetospora 奇嵌孢虫门奇嵌孢虫门孢子多细胞或单细胞,内含1个或多个孢质,无极囊或极丝主要为水生无脊椎动物的寄生虫纤毛虫门纤毛虫门 CiliophoraCili
5、ophora生活史一定阶段至少有纤毛或复合纤毛器,即使无纤毛时也存在表膜下纤毛系统,两型核无性生殖为横向二分裂,也有出芽和复分裂,有性生殖为接合生殖、自体受精和细胞受精通常有伸缩泡异养,大多数自由生活MicrosporaMicrospora 微孢子虫门微孢子虫门 孢子单细胞,壁无孔,含有单核或双核的孢质及简单或复杂的射出器,射出器有极管极管或极帽极帽,无线粒体全部寄生1.外膜2.中层膜3.内膜4.内质膜5.具二核6.后极泡7.极锚8.极体9.极丝10.极孔 Diagrammatic illustration of a cut away view through a microsporidian
6、 spore. Modified from Vavra, J. 1976. Structure of the Microsporidia. In L. A. Bulla and T. C. Cheng (Eds.), Comparative Pathobiology, Plenum Press, New York, 1:1-85 and from I. V. Issi (1986), Microsporidia as a phylum of parasitic protozoa, Acad. Sci. USSR “Protozoology” (Leningrad) 10:6-136. Abbr
7、eviations as above but including PB = posterior body, N = nucleus, VPL = Vesicular part of the polaroplast. (T. G. Andreadis) SEM of a germinated spore of Nosema algerae. (J. J. Becnel)SEM of meiospores of the microsporidium Parathelohania legeri from larvae of the mosquito Anopheles maculipennis (五
8、斑按蚊五斑按蚊). (J. J. Becnel)Light microscope interference contrast micrograph of a Vairimorpha species from the gypsy moth, Lymantria dispar. Uninucleate octospores. Note the presence of an interfacial envelope and that some packets contain fewer than 8 spores. (J. V. Maddox) Light microscope interferen
9、ce contrast micrograph of environ-mental spores of a Nosema species from the gypsy moth, Lymantria dispar. Fresh preparation, unstained. (J. V. Maddox)LM interference contrast micrograph of environmental spores of a Caudospora sp.(尾孢虫属) from a black fly larva (Prosimulium sp. 原蚋原蚋). Fresh preparatio
10、n, unstained. (J. V. Maddox)LM phase contrast micrograph of environmental spores of Edhazardia aedis from the mosquito Aedes aegypti. (T. G. Andreadis)LM phase contrast micrograph of a germinated uninucleate spore of Edhazardia aedis that is responsible for horizontal transmission. (J. J. Becnel)LM
11、interference contrast micrograph of the uninucleate, pyriform spore of Edhazardia aedis in an India ink preparation demonstrating the mucoca-lyx surrounding the spore. (J. J. Becnel) LM phase contrast micrograph of Thelohania (泰罗汉孢虫属) solenopsae from Solenopsis invicta. Both octospores and free spor
12、es are present. (J. J. Becnel)Light microscope phase contrast micrograph of spores of Ovavesicula popillae from the Japanese beetle, Popillia japonica. (T. G. Andreadis) LM phase contrast micrograph of Nosema lymantriae primary spores in the midgut epithelium. Fresh preparation, no stain. Primary sp
13、ores are responsible for transmitting the infection from one cell to another. Fresh preparation, unstained. (L. F. Solter)LM bright field micrograph of Nosema trichoplusiae from the cabbage looper, Trichoplusia ni. Spores were fixed in methanol and stained in aqueous Giemsa. (J. V. Maddox)LM bright
14、field micrograph of Nosema trichoplusiae from the cabbage looper, Trichoplusia ni. Spores were fixed in methanol and stained in aqueous Giemsa. (J. V. Maddox) LM bright field micrograph of Endoreticulatus (内网虫属) schubergi from the lawn webworm, Crambus trisectus (草草螟螟). Spores were fixed in methanol
15、 and stained in aqueous Giemsa. (J. V. maddox)LM bright micrograph of Nosema muscidifuracis in an infected cell of the hymenopteran parasitoid of the fly, Muscidifurax raptor. The cytoplasm contains sporoblasts, immature spores, and mature spores. Fixed in methanol and stained in aqueous Giemsa. (J.
16、 J. Becnel)Merogonic Cycle TEM of a diplokaryotic meront of Amblyospora connecticus from the mosquito Aedes cantator. (T. G. Andreadis)TEM of Vairimorpha necatrix from the armyworm, Pseudaletia unipuncta. Meront in midgut epithelial cell, 24 hours post infection. This meront could be uninucleate or
17、binucleate, depending on the plane of the section. (J. V. Maddox)LM bright field micrograph of Nosema bambycis in the silkworm Bombyx mori (家蚕家蚕). Binary fission of a meront in B. mori tissue culture. Giemsa stain. (R. Ishihara)Sporogonic Cycle TEM of the moniliform sporogonial plasmodium of Endoret
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