Literature DB >> 11719115

Further studies on an intermediate host murine model showing that a primary Echinococcus granulosus infection is protective against subsequent oncospheral challenge.

W Zhang1, H You, Z Zhang, G Turson, A Hasyet, D P McManus.   

Abstract

We describe the use of a murine model to evaluate resistance against subsequent challenge following a primary infection with oncospheres of Echinococcus granulosus. Mice (Kunming strain) were infected with hatched oncospheres of Echinococcus granulosus; 21 days later a second challenge was given by a different route of infection. A primary infection by intraperitoneal (i.p.) injection stimulated 100 and 90.5% protection in terms of reduced cyst numbers against a secondary infection given subcutaneously (s.c.) or intravenously (i.v.), respectively. A primary infection given s.c. followed by i.p. or i.v. challenge resulted in 84.0 and 100% protection, respectively. Intravenous infection followed by i.p. or s.c. challenge resulted in 98.5 and 69.4% protection, respectively. With the i.v. route of infection, almost all resultant cysts were present in the lungs. The data show that a primary infection with oncospheres can induce total or a high degree of protection against a subsequent challenge and confirms that natural (concomitant) immunity can be stimulated in the intermediate host as the result of a primary infection. This may explain the decline in hydatid infection in sheep older than 2 years in hyper-endemic areas such as those found in Xingjiang, China. These older sheep may have been earlier infected and have subsequently self-cured, with the primary infection stimulating an immune response that protects the intermediate host animals from further infection.

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Year:  2001        PMID: 11719115     DOI: 10.1016/s1383-5769(01)00086-1

Source DB:  PubMed          Journal:  Parasitol Int        ISSN: 1383-5769            Impact factor:   2.230


  6 in total

1.  Hydatid cyst formation in male Balb/c mice following the intraperitoneal injection of live protoscoleces and activated oncospheres: a comparative study.

Authors:  Sara Ahmadnia; Mohammad Moazeni; Soliman Mohammadi-Samani; Amir Mootabi Alavi
Journal:  J Parasit Dis       Date:  2012-11-06

2.  Humoral and cytokine response during protection of mice against secondary hydatidosis caused by Echinococcus granulosus.

Authors:  Khaled M Al-Qaoud; Sami K Abdel-Hafez
Journal:  Parasitol Res       Date:  2005-10-28       Impact factor: 2.289

3.  The Echinococcus granulosus antigen B gene family comprises at least 10 unique genes in five subclasses which are differentially expressed.

Authors:  Wenbao Zhang; Jun Li; Malcolm K Jones; Zhuangzhi Zhang; Li Zhao; David Blair; Donald Peter McManus
Journal:  PLoS Negl Trop Dis       Date:  2010-08-10

Review 4.  Concepts in immunology and diagnosis of hydatid disease.

Authors:  Wenbao Zhang; Jun Li; Donald P McManus
Journal:  Clin Microbiol Rev       Date:  2003-01       Impact factor: 26.132

5.  Natural infection of the ground squirrel (Spermophilus spp.) with Echinococcus granulosus in China.

Authors:  Yu Rong Yang; Tianxi Liu; Xueli Bai; Belgees Boufana; Philip S Craig; Minoru Nakao; Akira Ito; Jan Zhong Zhang; Patrick Giraudoux; Donald P McManus
Journal:  PLoS Negl Trop Dis       Date:  2009-09-22

6.  Recombinant antigens for immunodiagnosis of cystic echinococcosis.

Authors:  Jun Li; Wen-Bao Zhang; Donald P. McManus
Journal:  Biol Proced Online       Date:  2004-05-10       Impact factor: 3.244

  6 in total

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