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[云南大理对小土蜗、斯氏萝卜螺和尖膀胱螺进行肝片吸虫的实验性感染]

[Experimental infection of Galba pervia, Radix swinhoei and Physa acuta with Fasciola hepatica in Dali, Yunnan].

作者信息

Fang Wen, Li Tian-mei, Li Ke-rong, Chen Feng, Liu Yu-hua

出版信息

Zhongguo Ji Sheng Chong Xue Yu Ji Sheng Chong Bing Za Zhi. 2014 Aug;32(4):285-8.

Abstract

OBJECTIVE

To determine the intermediate host of Fasciola hepatica in Dali of Yunnan Province, and investigate its development and characteristics.

METHODS

F. hepatica eggs from cattle were collected from July 2012 to July 2013, and placed in 28 degrees C water bath for incubation. Galba pervia, Radix swinhoei, and Physa acuta were collected from Dali, and used to be infected with F. hepatica in the laboratory. Trematode infections were excluded from the snails before experiment. All the snails were infected with F. hepatica miracidia, reared in mud pots. Dead snails were dissected for observing the development of F. hepatica. The metacercariae were collected and identified by PCR amplification of partial sequence of mitochondrial cytochrome oxidase subunit I (COX1) gene.

RESULTS

A total of 1 146 R. swinhoei, 996 P. acuta, and 3 307 G. pervia snails were infected with F. hepatica, respectively. Mother rediae were found in two R. swinhoei snails, but no child rediae were observed in the snails. No larval forms were found in P. acuta. G. pervia was infected by F. hepatica with an infection rate of 27.2% (900/3307). The miracidium escaped from the egg and penetrated into G. pervia at temperature 22 degrees C, developed into a sporocyst after 7-15 days, which transformed into mother redia at the 11 st-20th day post-infection. The mother redia developed into daughter redia at the 30th-37th day, and produced cercaria with longtail, and became metacercaria at the 42nd-55th day. PCR confirmed that the metacercariae were that of F. hepatica, with an obvious band (approximately 500 bp).

CONCLUSION

Among the three potential intermediate hosts in Dali, G. pervia is experimentally infected with F. hepatica.

摘要

目的

确定云南省大理地区肝片吸虫的中间宿主,并研究其发育过程及特征。

方法

于2012年7月至2013年7月收集牛源肝片吸虫虫卵,置于28℃水浴中孵化。从大理采集小土蜗、斯氏萝卜螺和尖膀胱螺,在实验室用于感染肝片吸虫。实验前排除螺体内的吸虫感染。所有螺均感染肝片吸虫毛蚴,饲养于泥盆中。解剖死亡螺以观察肝片吸虫的发育情况。收集囊蚴并通过线粒体细胞色素氧化酶亚基I(COX1)基因部分序列的PCR扩增进行鉴定。

结果

分别有1146只斯氏萝卜螺、996只尖膀胱螺和3307只小土蜗感染肝片吸虫。在2只斯氏萝卜螺中发现了母雷蚴,但未在螺体内观察到子雷蚴。在尖膀胱螺中未发现幼虫形态。小土蜗被肝片吸虫感染,感染率为27.2%(900/3307)。毛蚴在22℃时从卵中逸出并侵入小土蜗,7 - 15天后发育为胞蚴,感染后第11 - 20天转变为母雷蚴。母雷蚴在第30 - 37天发育为子雷蚴,并产生长尾尾蚴,在第42 - 55天变为囊蚴。PCR证实囊蚴为肝片吸虫囊蚴,有明显条带(约500 bp)。

结论

在大理的三种潜在中间宿主中,小土蜗经实验感染了肝片吸虫。

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