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THE NATURAL HISTORY OF HUMAN POLIOMYELITIS : I. DISTRIBUTION OF VIRUS IN NERVOUS AND NON-NERVOUS TISSUES.人类脊髓灰质炎的自然史:I. 病毒在神经组织和非神经组织中的分布。
J Exp Med. 1941 May 31;73(6):771-93. doi: 10.1084/jem.73.6.771.
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Early interactions between poliovirus and ERK cells: some observations on the nature and significance of the rejected particles.脊髓灰质炎病毒与ERK细胞的早期相互作用:关于被排斥颗粒的性质和意义的一些观察
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Translocation of bacteriophage across the intestinal wall of the rat.
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The adsorption and early fate of purified poliovirus in HeLa cells.纯化脊髓灰质炎病毒在HeLa细胞中的吸附及早期转归
Virology. 1961 Apr;13:439-47. doi: 10.1016/0042-6822(61)90275-6.
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On the size of the toxic particle passing the intestinal barrier in botulism.关于肉毒中毒中通过肠道屏障的有毒颗粒大小
J Exp Med. 1960 Jun 1;111(6):745-59. doi: 10.1084/jem.111.6.745.
6
The dissemination of Salmonella typhi, S. paratyphi A and S. paratyphi B through the organs of the white mouse by oral infection.通过口服感染,伤寒沙门氏菌、甲型副伤寒沙门氏菌和乙型副伤寒沙门氏菌在小白鼠各器官中的传播。
J Hyg (Lond). 1960 Sep;58(3):307-19. doi: 10.1017/s0022172400038420.
7
Fate of bacteriophage particles introduced into mice by various routes.通过各种途径引入小鼠体内的噬菌体颗粒的命运。
Proc Soc Exp Biol Med. 1958 Jul;98(3):577-80. doi: 10.3181/00379727-98-24112.
8
Pathogenesis of poliomyelitis; reappraisal in the light of new data.脊髓灰质炎的发病机制;根据新数据重新评估。
Science. 1956 Jun 29;123(3209):1151-7. doi: 10.1126/science.123.3209.1151.
9
Viremia in experimental poliomyelitis. I. General aspects of infection after intravascular inoculation with strains of high and of low invasiveness.实验性脊髓灰质炎中的病毒血症。I. 经血管接种高侵袭性和低侵袭性毒株后的感染总体情况。
Am J Hyg. 1954 Nov;60(3):339-57.
10
Determinants of reovirus interaction with the intestinal M cells and absorptive cells of murine intestine.呼肠孤病毒与小鼠肠道M细胞及吸收细胞相互作用的决定因素。
Gastroenterology. 1983 Aug;85(2):291-300.

在猪回肠外植体中引发感染的柯萨奇病毒与细胞的相互作用。

Coxsackievirus-cell interactions that initiate infection in porcine ileal explants.

作者信息

Heinz B A, Cliver D O

机构信息

Food Research Institute, University of Wisconsin, Madison 53706.

出版信息

Arch Virol. 1988;101(1-2):35-47. doi: 10.1007/BF01314650.

DOI:10.1007/BF01314650
PMID:2843148
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7087173/
Abstract

Coxsackievirus B5 (CB5) labeled with tritiated uridine was used to trace the interaction of the virus with explant cultures of porcine ileum. Similarly labeled human poliovirus 1 (PO 1), which is not specifically retained by porcine tissue, was used as a control. The explant procedure employed could maintain ileal tissue in a differentiated state for up to 48 hours. Porcine ileum was acquired from both young (4-6 week-old) and adult (9-11 month-old) animals. Inoculated explants of either absorptive or lymphoid tissue were incubated at temperatures selected to permit either viral adsorption or penetration and elution to occur. Retention of radioactive virus was quantitated by liquid scintillation counting and localized by autoradiography. Only in absorptive tissue explants from young animals did adsorption of CB5 at 6 degrees C exceed penetration at 37 degrees C. This suggested that incubation at 6 degrees C may not be an appropriate condition for studying enterovirus adsorption in explants. CB5 penetrated most efficiently into lymphoid tissue explants from young animals, indicating that these tissues could discriminate between CB5 and PO 1. In explants from adults, CB5 penetrated equally well into lymphoid and absorptive tissues. Virus penetrated into the absorptive epithelial cells and, possibly, the lamina propria near the villous tips. Low efficiency of penetration, and the non-critical function of these target cells, may help account for the characteristic lack of gastrointestinal symptoms in enterovirus infections.

摘要

用氚标记尿苷的柯萨奇病毒B5(CB5)来追踪该病毒与猪回肠外植体培养物的相互作用。同样用氚标记的人脊髓灰质炎病毒1型(PO 1)作为对照,它不会被猪组织特异性保留。所采用的外植体操作程序可使回肠组织在分化状态下维持长达48小时。猪回肠取自幼年(4 - 6周龄)和成年(9 - 11月龄)动物。将接种后的吸收性或淋巴组织外植体在选定的温度下孵育,以允许病毒吸附、穿透和洗脱发生。通过液体闪烁计数对放射性病毒的保留情况进行定量,并通过放射自显影进行定位。仅在幼年动物的吸收性组织外植体中,6℃时CB5的吸附超过37℃时的穿透。这表明6℃孵育可能不是研究外植体中肠道病毒吸附的合适条件。CB5最有效地穿透到幼年动物的淋巴组织外植体中,表明这些组织能够区分CB5和PO 1。在成年动物的外植体中,CB5穿透到淋巴组织和吸收性组织的效率相同。病毒穿透到吸收性上皮细胞中,并且可能穿透到绒毛尖端附近的固有层。穿透效率低以及这些靶细胞的非关键功能,可能有助于解释肠道病毒感染中典型的缺乏胃肠道症状的现象。