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Series GSE20927 Query DataSets for GSE20927
Status Public on Mar 18, 2010
Title Localized complement activation in the development of protective immunity against Ostertagia ostertagi infections in cattle
Organism Bos taurus
Experiment type Expression profiling by array
Summary The gastrointestinal nematode Ostertagia ostertagi is one of major causal agents that contribute to production inefficiency in cattle industry in the temperate region of the world. One of pathophysiological factors that lead to reduced weight gain and milk yield is altered gastrointestinal functions, resulting from considerable tissue damage in the abomasal mucosa during infections. Protective immunity to Ostertagia ostertagi infections in cattle develops very slowly. Resistance to reinfection becomes manifest only after a prolonged period of exposure. Mechanisms underlying the development of protective immunity remain largely unexplored. Immune animals, with significantly reduced worm burdens, were developed after multiple drug-attenuated experimental infections and were compared to the primary infected group and their respective uninfected controls. In this study, transcriptomic analysis identified 3 signaling pathways, the complement system, leukocyte extravasation and acute phase responses, significantly impacted during both primary and repeat infections. The markedly increased mRNA levels of complement components C3, factor B (CFB), and factor I (CFI) in the abomasal mucosa of the infected cattle were confirmed using quantitative PCR. Western blot analysis established the presence of elevated levels of activated C3 proteins in the mucosa. One of the iniators of local complement activation could be related with secretory IgA and IgM because infections significantly upregulated expression of J chain (IGJ) as well as polymeric Ig receptor (PIGR) and an IgM-specific receptor (FAIM3), suggesting sustained increase in both synthesis and transepithelial transport of IgA and IgM during the infection. The elevated levels of pro-inflammatory cytokines, such as IL-4 and IL-1β, during the infection may be involved in gene regulation of complement components. Our data suggested enhanced tissue repair and mucin secretion in immune animals may also contribute to protective immunity. Our results presented the first piece of evidence that local complement activation may be involved in the development of long term protective immunity and provided a novel mechanistic insight into resistance against Ostertagia ostertagi in cattle.
 
Overall design There were four treatment groups: naive control (never infected), primary infection, drug-attenuated control, and drug-attenuated 5th reinfection. Each group had 4 biolgical replicates. A total of 16 arrays were used for this experiment. The 2 major contrast were 1). The primary infection vs naive control; and 2). The drug-attenuated 5th reinfection vs the drug-attenuated control.
 
Contributor(s) Li RW, Hou Y, Li C, Gasbarre LC
Citation(s) 20884121
Submission date Mar 17, 2010
Last update date Mar 22, 2012
Contact name Robert W Li
E-mail(s) robert.li@ars.usda.gov
Phone 301-504-5185
Fax 301-504-8414
Organization name USDA
Department Animal & Natural Resources Institute
Lab Bovine Functional Genomics Laboratory
Street address Barc East
City Beltsville
State/province MD
ZIP/Postal code 20705
Country USA
 
Platforms (1)
GPL3301 USDA Bovine 60mer 344k Array (gene layout)
Samples (16)
GSM523024 The abomasal mucosa of calf#952 infected with Ostertagia ostertagi for 14 days
GSM523164 The abomasal mucosa of calf#953 uninfected
GSM523165 The abomasal mucosa of calf#954 infected with Ostertagia ostertagi for 14 days
Relations
BioProject PRJNA124365

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Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE20927_RAW.tar 27.9 Mb (http)(custom) TAR (of TXT)
Processed data included within Sample table

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