2006
DOI: 10.1016/j.molbiopara.2006.02.009
|View full text |Cite
|
Sign up to set email alerts
|

Biomphalaria glabrata cytosolic copper/zinc superoxide dismutase (SOD1) gene: Association of SOD1 alleles with resistance/susceptibility to Schistosoma mansoni

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
4
1

Citation Types

1
79
1
1

Year Published

2007
2007
2020
2020

Publication Types

Select...
6
4

Relationship

0
10

Authors

Journals

citations
Cited by 74 publications
(82 citation statements)
references
References 30 publications
1
79
1
1
Order By: Relevance
“…A similar system has been demonstrated to be a major molecular mechanism for resistance of the freshwater snail, B. glabrata to the parasite S. mansoni is due to deficient forms of anti-oxidant enzymes in the respiratory burst pathway [35]. Resistant B. glabrata generate significantly more H 2 O 2 than susceptible snails [29] and this increased concentration of H 2 O 2 generated by resistant snails has been correlated to higher expression levels of the SOD1 transcript [36]. Expression of the SOD1 transcript was later found to be associated with one allele found in resistant snails [37].…”
Section: Differential Expression Of Two Anti-oxidant Enzymes Potentiamentioning
confidence: 91%
“…A similar system has been demonstrated to be a major molecular mechanism for resistance of the freshwater snail, B. glabrata to the parasite S. mansoni is due to deficient forms of anti-oxidant enzymes in the respiratory burst pathway [35]. Resistant B. glabrata generate significantly more H 2 O 2 than susceptible snails [29] and this increased concentration of H 2 O 2 generated by resistant snails has been correlated to higher expression levels of the SOD1 transcript [36]. Expression of the SOD1 transcript was later found to be associated with one allele found in resistant snails [37].…”
Section: Differential Expression Of Two Anti-oxidant Enzymes Potentiamentioning
confidence: 91%
“…Although the current understanding of schistosome and snail biology during the infection process is still incomplete, especially regarding the snail immunity (Bayne, 2009), a variety of molecules have been identified and may be associated with schistosome survival or snail defense mechanisms, including certain proteolytic enzymes such as cysteine proteases (Lodes and Yoshino, 1989;Guillou et al, 2007a;Humphries and Yoshino, 2008;Ittiprasert et al, 2010), receptor recognition molecules (e.g., fibrinogen-related proteins (FREPs) and lectin (Johnston and Yoshino, 2001;Hertel et al, 2005;Zhang et al, 2007;Ittiprasert et al, 2010)), molecules related to cell adhesion and signaling pathways (Goodall et al, 2006;Lockyer et al, 2007b;Zhang et al, 2007;Ittiprasert et al, 2010), and immune regulation-like epitope mimics (Plows et al, 2005;Lockyer et al, 2007b;Lehr et al, 2008). Most of the above studies aimed to decipher the differences in gene regulation between schistosome-resistant and schistosome-susceptible snails, focusing on the acute stage of schistosome-snail infection (within minutes to hours of the infection) but not chronic infection (up to >2 months) (Bayne, 2009).…”
Section: Introductionmentioning
confidence: 99%
“…icCuZnSODs cDNA have been cloned from some invertebrate and vertebrate species [19][20][21][22][23][24][25][26][27][28]. However, little is known about their genomic features, immune responses against biological infections and characterization of the recombination protein.…”
Section: Introductionmentioning
confidence: 99%