Identification of differentially expressed genes in Oncomelania hupensis chronically infected with Schistosoma japonicum

被引:7
作者
Wang, Hao [2 ]
Zhao, Qin Ping [1 ,2 ]
Nie, Pin [1 ]
Sen Jiang, Ming [2 ]
Song, Jian [2 ]
机构
[1] Chinese Acad Sci, State Key Lab Freshwater Ecol & Biotechnol, Inst Hydrobiol, Wuhan 430072, Hubei Province, Peoples R China
[2] Wuhan Univ, Sch Basic Med Sci, Wuhan 430071, Hubei Province, Peoples R China
关键词
Oncomelania hupensis; Suppression subtractive hybridization; Schistosoma japonicum; Chronic infection; Schistosome-snail interaction; Head-foot; SNAIL BIOMPHALARIA-GLABRATA; GLABRATA/ECHINOSTOMA-CAPRONI MODEL; MANSONI; RESISTANT; HEMOCYTES; PROTEINS; COMPATIBILITY; MIRACIDIA; PARASITES; DEFENSE;
D O I
10.1016/j.exppara.2012.02.004
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
Oncomelania hupensis is the unique intermediate host of Schistosoma japonicum. The schistosome-snail interaction is biomedically important. To identify differentially expressed transcripts in O. hupensis chronically infected with S. japonicum, suppression subtractive hybridization (SSH) was used to construct a cDNA library in each direction for transcripts that are more abundantly enriched in head-foot part of the infected O. hupensis and for those that are more abundantly enriched in the uninfected, as head-foot part contains hemocytes and hemolymph which are associated with the snail internal defense system. After differential screening, 39 transcripts were identified, including nine and 30 transcripts enriched in infected and uninfected snails, respectively. Some of the transcripts have similar homology to available sequences in current databases, including transposase, caveolin-like protein, pancreatic trypsin inhibitor-like protein, prosaposin, glutathione s-transferase (GST), and several hypothetical proteins, while most of the transcripts do not match with any sequences in available databases. The identified transcripts were involved functionally in cell growth, metabolism, signal transduction, and immune responses. Two forward library transcripts and 11 reverse library transcripts were selected for real-time PCR, and 10 of them were confirmed to be consistent with the SSH results. It is intriguing to continue functional studies for some genes such as pancreatic trypsin inhibitor; a hypothetical protein (HS576367) related to calcium ion binding; GST; and several unknown proteins (HS576353 and HS576355). These identified differentially expressed genes may be key targets for understanding the molecular mechanism of co-existence during which the snail is unable to rid itself of the schistosome in chronic infection stage. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:374 / 383
页数:10
相关论文
共 50 条
[41]   Comparative studies of the defense mechanism against Schistosoma japonicum of schistosome-susceptible and -resistant Oncomelania nosophora [J].
Sasaki, Y ;
Kirinoki, M ;
Chigusa, Y .
PARASITOLOGY INTERNATIONAL, 2005, 54 (03) :157-165
[42]   Comparative studies on the internal defense system of schistosome-resistant and -susceptible amphibious snail Oncomelania nosophora 1.: Comparative morphological and functional studies on hemocytes from both snails [J].
Sasaki, Y ;
Furuta, E ;
Kirinoki, M ;
Seo, N ;
Matsuda, H .
ZOOLOGICAL SCIENCE, 2003, 20 (10) :1215-1222
[43]   An insight into the genetic variation of Schistosoma japonicum in mainland China using DNA microsatellite markers [J].
Shrivastava, J ;
Qian, BZ ;
Mcvean, G ;
Webster, JP .
MOLECULAR ECOLOGY, 2005, 14 (03) :839-849
[44]   Are Biomphalaria snails resistant to Schistosoma mansoni? [J].
Théron, A ;
Coustau, C .
JOURNAL OF HELMINTHOLOGY, 2005, 79 (03) :187-191
[45]   The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools [J].
Thompson, JD ;
Gibson, TJ ;
Plewniak, F ;
Jeanmougin, F ;
Higgins, DG .
NUCLEIC ACIDS RESEARCH, 1997, 25 (24) :4876-4882
[46]   Characterisation of proteins differentially present in the plasma of Biomphalaria glabrata susceptible or resistant to Echinostoma caproni [J].
Vergote, D ;
Bouchut, A ;
Sautière, PE ;
Roger, E ;
Galinier, R ;
Rognon, A ;
Coustau, C ;
Salzet, M ;
Mitta, G .
INTERNATIONAL JOURNAL FOR PARASITOLOGY, 2005, 35 (02) :215-224
[47]  
Webster J.P., 2004, AM NAT, V164, P33, DOI DOI 10.1086/424607
[48]   PENETRATION AND MIGRATION ROUTES OF SCHISTOSOMA-JAPONICUM MIRACIDIA IN THE SNAIL ONCOMELANIA-HUPENSIS [J].
XIA, MY ;
JOURDANE, J .
PARASITOLOGY, 1991, 103 :77-83
[49]   Characterization of immune genes from the schistosome host snail Biomphalaria glabrata that encode peptidoglycan recognition proteins and gram-negative bacteria binding protein [J].
Zhang, Si-Ming ;
Zeng, Yong ;
Loker, Eric S. .
IMMUNOGENETICS, 2007, 59 (11) :883-898
[50]   Differential expression of genes in salivary glands of male Rhipicephalus (Boophilus)microplus in response to infection with Anaplasma marginale [J].
Zivkovic, Zorica ;
Esteves, Eliane ;
Almazan, Consuelo ;
Daffre, Sirlei ;
Nijhof, Ard M. ;
Kocan, Katherine M. ;
Jongejan, Frans ;
de la Fuente, Jose .
BMC GENOMICS, 2010, 11