Dubey J P
J Protozool. 1979 Aug;26(3):433-43. doi: 10.1111/j.1550-7408.1979.tb04650.x.
The endogenous development of Isospora rivolta (Grassi) was studied in cats fed oocysts, and was compared with the endogenous cycle after feeding them mice infected with I. rivolta. For the mouse-induced cycle, 14 newborn cats were killed 12 to 240 h after having been fed mesenteric lymph nodes and spleens ofmice. Asexual and sexual development occurred throughout the small intestine, in epithelial cells of the villi and glands of Lieberkühn. The number of asexual generations was not determined with certainty, but there were at least 3 structurally different meronts. Type I meronts appeared at 12-48 h postinoculation (HPT). They were 8.5(6-13) x 5.1(3-6) micrometer, contained 2-8 merozoites, and divide by binary division or endodyogeny. Type II meronts were multinucleate merozoite-shaped meronts within a single parasitophorous vacuole. They were found at 48-172 HPI and measured 12.6(9-18) x 9.8(9-13) micrometer. Individual multinucleate merozoite-shaped meronts were 7-13 x 3-5 micrometer in sections and contained 2-30 slender (5.5 x 1.0 micrometer) merozoites. Type III meronts occurred at 72-192 HPI and gamonts at 72-96 HPI. Mature microgamonts measured 11.3(9-15) x 8.0(6-9) micrometer in sections and up to 21.5 x 14 micrometer in smears, and contained up to 70 microgametes. Macrogamonts measured 13.3(11-18) x 9.0(5-13) micrometer in sections and 18 x 16 micrometer in smears, and contained up to 70 microgametes. Macrogamonts measured 13.3(11-18) x 9.0(5-13) micrometer. Sporulation was completed within 24 h at 22-26 C. For the study of the oocyst-induced cycle in cats, 18 newborn cats were killed between 6 and 192 HPI. The endogenous development was essentially similar to the mouse-induced cycle, but merogony and gametogony occurred 12-48 h later than in the latter cycle. Isospora rivolta was pathogenic for newborn but not for weaned cats. Newborn cats fed 10(6) sporocysts or infected mice usually developed diarrhea 3-4 days after inoculation. Microscopically, desquamation of the tips of the villi and cryptitis were seen in the ilium and cecum in association with meronts and gamonts. For the study of the development of I. rivolta in mice, mice were killed from day 1 to 23 months after having been fed 10(5)-10(6) sporocysts, and their tissues were examined for the parasites microscopically, and by feeding to cats. The following conclusions were drawn. (A) Isospora rivolta most freqeuntly invaded the mesenteric lymph nodes ofmice and remained there for 23 months at least. Ii also invaded the spleen, liver, and skeletal muscles of mice. This species could not be passed from mouse to mouse. Sporozoites increased in size from approximately 6.8 x 4.9 micrometer on day 1 to approximately 13.4 x 6.9 micrometer on day 31 postinoculation. Division was not seen. Prepatent period was 4-7 days and patent periods ranged from 2 to several weeks.
用卵囊感染猫,研究了里氏等孢球虫(格拉西)的内源性发育,并将其与用感染里氏等孢球虫的小鼠喂食猫后的内源性发育周期进行了比较。对于小鼠诱导的发育周期,在给14只新生猫喂食感染里氏等孢球虫小鼠的肠系膜淋巴结和脾脏后12至240小时处死。无性和有性发育发生在整个小肠,在绒毛上皮细胞和利伯屈恩腺中。无性世代的数量尚未确定,但至少有3种结构不同的裂殖体。I型裂殖体在接种后12 - 48小时出现。它们大小为8.5(6 - 13)×5.1(3 - 6)微米,含2 - 8个裂殖子,通过二分裂或内二分裂进行分裂。II型裂殖体是单个寄生泡内的多核裂殖子形裂殖体。它们在接种后48 - 172小时被发现,大小为12.6(9 - 18)×9.8(9 - 13)微米。在切片中,单个多核裂殖子形裂殖体大小为7 - 13×3 - 5微米,含2 - 30个细长(5.5×1.0微米)的裂殖子。III型裂殖体在接种后72 - 192小时出现,配子体在接种后72 - 96小时出现。成熟的小配子体在切片中大小为11.3(9 - 15)×8.0(6 - 9)微米,涂片上可达21.5×14微米,含多达70个小配子。大配子体在切片中大小为13.3(11 - 18)×9.0(5 - 13)微米,涂片上为18×16微米,含多达70个小配子。大配子体大小为13.3(11 - 18)×9.0(5 - 13)微米。在22 - 26℃下,24小时内完成孢子化。为研究猫体内卵囊诱导的发育周期,在接种后6至192小时处死18只新生猫。内源性发育与小鼠诱导的发育周期基本相似,但裂体增殖和配子生殖比后者晚12 - 48小时发生。里氏等孢球虫对新生猫有致病性,但对断奶猫无致病性。喂食10⁶个孢子囊或感染小鼠的新生猫通常在接种后3 - 4天出现腹泻。显微镜下,在回肠和盲肠可见绒毛顶端的脱屑和隐窝炎,伴有裂殖体和配子体。为研究里氏等孢球虫在小鼠体内的发育,给小鼠喂食10⁵ - 10⁶个孢子囊后,在第1天至23个月处死小鼠,对其组织进行显微镜检查以及喂给猫来检测寄生虫。得出以下结论。(A)里氏等孢球虫最常侵入小鼠的肠系膜淋巴结,至少在那里停留23个月。它也侵入小鼠的脾脏、肝脏和骨骼肌。该物种不能在小鼠之间传播。接种后第1天,子孢子大小约为6.8×4.9微米,到第31天增大到约13.4×6.9微米。未见分裂。潜隐期为4 - 7天,排虫期为2至数周。