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一种检测水和污水中人类轮状病毒方法的开发。

Development of a method for detection of human rotavirus in water and sewage.

作者信息

Smith E M, Gerba C P

出版信息

Appl Environ Microbiol. 1982 Jun;43(6):1440-50. doi: 10.1128/aem.43.6.1440-1450.1982.

Abstract

The simian rotavirus SA11 was used to develop a simple, reliable, and efficient method to concentrate rotavirus from tap water, treated sewage, and raw sewage by absorption to and elution from Filterite fiberglass-epoxy filters. SA11 adsorbed optimally to Filterite filters from water containing 0.5 mM AlCl3 at pH 3.5. Filter-bound virus was eluted with 0.05 M glycine-NaOH supplemented with 10% tryptose phosphate broth at pH 10. SA11 was quantitated by plaque assay, whereas human rotavirus was detected by immunofluorescence. The method was applied to detect rotavirus in raw and treated sewage at two Houston, Tex., sewage treatment plants. The sewage isolates were identified as rotavirus, probably a human strain, based on several criteria. The sewage isolates were detectable by an immunofluorescence test, using anti-SA11 serum which would detect the simian, human bovine, and porcine rotaviruses. No reaction was noted by immunofluorescence with the reoviruses or several common enteroviruses. The sewage isolates were neutralized by convalescent sera from a human adult and infant who had been infected by rotavirus as well as by a hyperimmune serum prepared in guinea pigs against purified human rotavirus. Preimmune or preillness sera did not react with the isolates by neutralization or immunofluorescence. The natural isolates were sensitive to pH 11 and other inactivating agents, similar to SA11. The buoyant density of the sewage isolates in CsCl gradients was 1.36 g/cm3, which is the value usually reported for complete, infectious rotavirus particles. The double-shelled particle diameter was 67.1 +/- 2.4 nm. Finally, electron micrographs of cell lysates inoculated with the sewage isolate showed particles displaying characteristic rotavirus morphology.

摘要

猿猴轮状病毒SA11被用于开发一种简单、可靠且高效的方法,通过吸附到Filterite玻璃纤维 - 环氧树脂滤器上并从其上洗脱,从自来水、处理后的污水和原污水中浓缩轮状病毒。SA11在pH 3.5、含有0.5 mM AlCl3的水中能最佳地吸附到Filterite滤器上。用pH 10、补充有10%胰蛋白胨磷酸盐肉汤的0.05 M甘氨酸 - 氢氧化钠洗脱结合在滤器上的病毒。SA11通过蚀斑试验进行定量,而人轮状病毒则通过免疫荧光检测。该方法被应用于检测得克萨斯州休斯顿市两家污水处理厂的原污水和处理后污水中的轮状病毒。基于多项标准,污水分离株被鉴定为轮状病毒,可能是一种人类毒株。使用能检测猿猴、人类、牛和猪轮状病毒的抗SA11血清,通过免疫荧光试验可检测到污水分离株。用呼肠孤病毒或几种常见肠道病毒进行免疫荧光试验未发现反应。污水分离株能被一名感染过轮状病毒的成人和婴儿的恢复期血清以及在豚鼠中制备的针对纯化人轮状病毒的超免疫血清中和。免疫前或发病前血清通过中和试验或免疫荧光试验与分离株无反应。天然分离株对pH 11和其他灭活剂敏感,与SA11相似。在CsCl梯度中污水分离株的浮力密度为1.36 g/cm³,这是通常报道的完整感染性轮状病毒颗粒的值。双层颗粒直径为67.1±2.4 nm。最后,接种了污水分离株的细胞裂解物的电子显微镜照片显示出具有特征性轮状病毒形态的颗粒。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d6f/244252/dee5e720b8bc/aem00187-0230-a.jpg

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