Correlative Gene Expression to Protective Seroconversion in Rift Valley Fever Vaccinates

Rift Valley fever Virus (RVFV), a negative-stranded RNA virus, is the etiological agent of the vector-borne zoonotic disease, Rift Valley fever (RVF). In both humans and livestock, protective immunity can be achieved through vaccination. Earlier and more recent vaccine trials in cattle and sheep dem...

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Published inPloS one Vol. 11; no. 1; p. e0147027
Main Authors Laughlin, Richard C, Drake, Kenneth L, Morrill, John C, Adams, L Garry
Format Journal Article
LanguageEnglish
Published United States Public Library of Science 19.01.2016
Public Library of Science (PLoS)
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Summary:Rift Valley fever Virus (RVFV), a negative-stranded RNA virus, is the etiological agent of the vector-borne zoonotic disease, Rift Valley fever (RVF). In both humans and livestock, protective immunity can be achieved through vaccination. Earlier and more recent vaccine trials in cattle and sheep demonstrated a strong neutralizing antibody and total IgG response induced by the RVF vaccine, authentic recombinant MP-12 (arMP-12). From previous work, protective immunity in sheep and cattle vaccinates normally occurs from 7 to 21 days after inoculation with arMP-12. While the serology and protective response induced by arMP-12 has been studied, little attention has been paid to the underlying molecular and genetic events occurring prior to the serologic immune response. To address this, we isolated RNA from whole blood of vaccinated calves over a time course of 21 days before and after vaccination with arMP-12. The time course RNAs were sequenced by RNASeq and bioinformatically analyzed. Our results revealed time-dependent activation or repression of numerous gene ontologies and pathways related to the vaccine induced immune response and its regulation. Additional bioinformatic analyses identified a correlative relationship between specific host immune response genes and protective immunity prior to the detection of protective serum neutralizing antibody responses. These results contribute an important proof of concept for identifying molecular and genetic components underlying the immune response to RVF vaccination and protection prior to serologic detection.
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Conceived and designed the experiments: LGA JCM RCL. Performed the experiments: LGA JCM RCL. Analyzed the data: KLD RCL JCM LGA. Contributed reagents/materials/analysis tools: JCM KLD. Wrote the paper: RCL KLD LGA JCM.
Current address: Department of Biological and Health Sciences, Texas A&M University Kingsville, Kingsville, TX 78353, United States of America
Competing Interests: The commercial affiliation with Seralogix LLC does not alter the authors' adherence to PLOS ONE policies on sharing data and materials.
ISSN:1932-6203
1932-6203
DOI:10.1371/journal.pone.0147027