PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
April 1, 2016Virology Journal113 citationsOpen Access

S1 domain of the porcine epidemic diarrhea virus spike protein as a vaccine antigen

NMNirajkumar MakadiyaRBRobert BrownlieJHJan van den Hurk

Key Result

Maternal vaccination with the recombinant PEDV S1 subunit vaccine significantly increased the survival rate of suckling piglets to 87.5% compared to 42.9% in the control group after PEDV challenge.

Structured PICO

Does vaccination of pregnant sows with recombinant PEDV S1 protein protect their suckling piglets from PEDV challenge?

P
Population
Pregnant sows (n=2) and their suckling piglets (n=15; 8 from vaccinated sow, 7 from control sow), as well as yeast, insect, and mammalian cell lines for protein expression.
I
Intervention
Recombinant PEDV S1 protein (400 μg per dose) mixed with TriAdj adjuvant, administered intramuscularly to a pregnant sow three times (days 0, 14, and 28).
C
Comparator
Saline mixed with TriAdj adjuvant administered intramuscularly to a control pregnant sow.
O
Outcome
Protective efficacy in piglets after oral challenge with live PEDV, including clinical scores, fecal scores (diarrhea), weight, survival, and virus shedding.hard clinical

Vaccination of a pregnant sow with recombinant PEDV S1 protein induced lactogenic immunity that partially protected suckling piglets from mortality, but failed to prevent diarrhea or viral shedding.

Main Result

Absolute Event Rate: 87.5% vs 42.9%

p-value: p=0.0002

Limitations

  • Small sample size involving only two sows
  • Vaccine had negligible effect in preventing diarrhea or PEDV-mediated weight loss
  • Vaccine failed to provide complete protection to suckling piglets
  • Small sample size (only two sows used)
  • Vaccine failed to provide complete protection (no significant differences in diarrhea, body weight, and virus shedding)

Abstract

BACKGROUND: Porcine epidemic diarrhea virus (PEDV) is a highly contagious virus infecting pigs of all ages with high morbidity and mortality among newborn piglets. Currently, there is no effective vaccine available to protect the pigs from PEDV. The N-terminal subunit of spike protein (S1) is responsible for virus binding to the cellular receptor and contains a number of neutralizing antibody epitopes. Thus, we expressed and produced recombinant S1 protein to protect newborn piglets by immunization of sows. METHODS: Affinity tagged PEDV S1 protein was expressed in a secretory form in yeast, insect and mammalian cells to identify the most suitable production system. Purified recombinant protein was analysed by SDS-PAGE, Western blot and deglycosylation assay. A pregnant sow was intramuscularly immunized three times with adjuvanted recombinant protein prior to farrowing. PEDV-specific immune responses in sera and colostrum of the sow and piglets were assayed by ELISA and virus neutralization assays. Piglets were challenged orally with PEDV, and clinical parameters were monitored for 6 days post-challenge. RESULTS AND CONCLUSION: Of three eukaryotic expression systems tested (yeast, insect-cell, and mammalian), expression by HEK-293 T cells gave the highest yield of protein that was N-glycosylated and was the most appropriate candidate for vaccination. Administration of the subunit vaccine in a sow resulted in induction of S1-specific IgG and IgA that were passively transferred to the suckling piglets. Also, high virus neutralization titres were observed in the serum of the vaccinated sow and its piglets. After PEDV challenge, piglets born to the vaccinated sow exhibited less severe signs of disease and significantly lower mortality compared to the piglets of a control sow. However, there were no significant differences in diarrhea, body weight and virus shedding. Thus, vaccination with S1 subunit vaccine failed to provide complete protection to suckling piglets after challenge exposure, and further improvements are needed for the development of a subunit vaccine that fully protects against PEDV infection.

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

Makadiya et al. (2016) studied Porcine epidemic diarrhea virus (PEDV) infection (n=17). Recombinant PEDV S1 protein subunit vaccine vs. Saline with adjuvant was evaluated on Piglet survival at 6 days post-challenge (p=0.0002). Maternal vaccination with the recombinant PEDV S1 subunit vaccine significantly increased the survival rate of suckling piglets to 87.5% compared to 42.9% in the control group after PEDV challenge.

synapsesocial.com/papers/6a0856daab15ea61dee8c8f4https://doi.org/10.1186/s12985-016-0512-8
Ask AI
Helpful
Bookmark
Share
View Full Paper