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American journal of veterinary research2001; 62(8); 1307-1313; doi: 10.2460/ajvr.2001.62.1307

Evaluation of equine immunoglobulin specific for Rhodococcus equi virulence-associated proteins A and C for use in protecting foals against Rhodococcus equi-induced pneumonia.

Abstract: To determine whether purified equine immunoglobulin specific for Rhodococcus equi virulence-associated proteins A and C (VapA and VapC) can confer passive protection against R. equi-induced pneumonia in foals. Methods: Twenty-eight 3-week-old mixed-breed pony foals. Methods: 7 foals received IV injections of equine hyperimmune plasma (HIP) against whole-cell R. equi, and 7 received purified equine immunoglobulin specific for VapA and VapC 1 day prior to intrabronchial infection with R. equi strain 103+. Eleven foals were not treated prior to infection, and 3 control foals were neither treated nor infected. Heart rate, respiratory rate, and rectal temperature were recorded twice daily, and serum fibrinogen concentration and WBC count were determined every other day following infection. Foals were euthanatized 14 days following infection, and lung lesions and concentration of R. equi in lungs were assessed. Results: The onset of clinical signs of pneumonia was significantly delayed in the HIP- and immunoglobulin-treated groups, compared with the untreated infected group. Moreover, pulmonary lesions were less severe in the treated groups, and significantly fewer R. equi organisms were cultured from the lungs of treated foals. Conclusions: Degree of protection against R. equi-induced pneumonia provided by purified immunoglobulin specific for VapA and VapC was similar to that provided by commercially available HIP. Results not only suggest that immunoglobulin is the primary component of HIP that confers protection against R. equi-induced pneumonia in foals but also indicate that antibodies against R. equi VapA and VapC are protective.
Publication Date: 2001-08-11 PubMed ID: 11497456DOI: 10.2460/ajvr.2001.62.1307Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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The research investigated if equine immunoglobulin specifically targeting Rhodococcus equi virulence-associated proteins A and C (VapA and VapC) could protect foals against pneumonia caused by R. equi. The study reveals that this targeted immunoglobulin provided a similar level of protection to the commercially available hyperimmune plasma (HIP), suggesting that immunoglobulin is a major protective component in HIP.

Methodology

  • The study involved twenty-eight 3-week-old mixed-breed pony foals divided into four groups.
  • One group received intravenous injections of equine hyperimmune plasma (HIP), which is traditionally used against whole-cell R. equi.
  • Another group received purified equine immunoglobulin targeting VapA and VapC, proteins associated with the virulence of R. equi.
  • The injections were given one day before the foals were infected with a strain of R. equi via their bronchial tubes.
  • Eleven foals received no treatment before being subjected to the infection.
  • The last group of three foals was the control group, which remained uninfected and untreated.
  • Once the infection was established, researchers monitored the foals through daily measurements of heart rate, respiratory rate, rectal temperature while performing complete blood counts (including white blood cells) and fibrinogen concentration in the serum every other day.
  • Fourteen days after infection, the foals were euthanized, and their lungs were assessed for lesions and for the concentration of R.equi.

Results of the Study

  • The onset of pneumonia symptoms was significantly delayed in the foals that received HIP and the VapA and VapC-specific immunoglobulin.
  • The lung lesions in the treated foals were less severe than those in the untreated group, and fewer R. equi organisms were cultured from the lungs of the treated animals.

Conclusions of the Study

  • The research concludes that the purified immunoglobulin specifically targeting R. equi proteins — VapA and VapC — produced a similar degree of protection against R. equi-induced pneumonia as HIP.
  • These findings suggest that the immunoglobulin is the primary component in HIP that confers protection against pneumonia caused by R. equi in foals.
  • It also indicates that antibodies targeting R. equi’s VapA and VapC proteins have protective properties, providing a potential new avenue for preventive treatments.

Cite This Article

APA
Hooper-McGrevy KE, Giguere S, Wilkie BN, Prescott JF. (2001). Evaluation of equine immunoglobulin specific for Rhodococcus equi virulence-associated proteins A and C for use in protecting foals against Rhodococcus equi-induced pneumonia. Am J Vet Res, 62(8), 1307-1313. https://doi.org/10.2460/ajvr.2001.62.1307

Publication

ISSN: 0002-9645
NlmUniqueID: 0375011
Country: United States
Language: English
Volume: 62
Issue: 8
Pages: 1307-1313

Researcher Affiliations

Hooper-McGrevy, K E
  • Department of Pathobiology, Ontario Veterinary College, University of Guelph, Canada.
Giguere, S
    Wilkie, B N
      Prescott, J F

        MeSH Terms

        • Actinomycetales Infections / immunology
        • Actinomycetales Infections / prevention & control
        • Actinomycetales Infections / veterinary
        • Actinomycetales Infections / virology
        • Animals
        • Antibodies, Bacterial / blood
        • Antibodies, Bacterial / immunology
        • Antibody Specificity
        • Bacterial Proteins / immunology
        • Body Temperature
        • Fibrinogen / analysis
        • Heart Rate
        • Horse Diseases / immunology
        • Horse Diseases / prevention & control
        • Horse Diseases / virology
        • Horses
        • Immunoglobulins / immunology
        • Leukocyte Count / veterinary
        • Lipoproteins / immunology
        • Lung / microbiology
        • Male
        • Membrane Glycoproteins / immunology
        • Pneumonia, Bacterial / immunology
        • Pneumonia, Bacterial / prevention & control
        • Pneumonia, Bacterial / veterinary
        • Pneumonia, Bacterial / virology
        • Random Allocation
        • Recombinant Proteins
        • Respiration
        • Rhodococcus equi / immunology
        • Virulence Factors

        Citations

        This article has been cited 11 times.
        1. Harvey AB, Bordin AI, Rocha JN, Bray JM, Cohen ND. Opsonization but not pretreatment of equine macrophages with hyperimmune plasma nonspecifically enhances phagocytosis and intracellular killing of Rhodococcus equi. J Vet Intern Med 2021 Jan;35(1):590-596.
          doi: 10.1111/jvim.16002pubmed: 33326149google scholar: lookup
        2. Erganis O, Sayin Z, Hadimli HH, Sakmanoglu A, Pinarkara Y, Ozdemir O, Maden M. The effectiveness of anti-R. equi hyperimmune plasma against R. equi challenge in thoroughbred Arabian foals of mares vaccinated with R. equi vaccine. ScientificWorldJournal 2014;2014:480732.
          doi: 10.1155/2014/480732pubmed: 24982958google scholar: lookup
        3. Lohmann KL, Lopez AM, Manning ST, Marques FJ, Brownlie R, Allen AL, Sangster AE, Mutwiri G, Gerdts V, Potter A, Townsend HG. Failure of a VapA/CpG oligodeoxynucleotide vaccine to protect foals against experimental Rhocococcus equi pneumonia despite induction of VapA-specific antibody and interferon-γ response. Can J Vet Res 2013 Jul;77(3):161-9.
          pubmed: 24101791
        4. Oliveira AF, Ruas LP, Cardoso SA, Soares SG, Roque-Barreira MC. Vaccination of mice with salmonella expressing VapA: mucosal and systemic Th1 responses provide protection against Rhodococcus equi infection. PLoS One 2010 Jan 13;5(1):e8644.
          doi: 10.1371/journal.pone.0008644pubmed: 20072623google scholar: lookup
        5. Jacks S, Giguère S, Crawford PC, Castleman WL. Experimental infection of neonatal foals with Rhodococcus equi triggers adult-like gamma interferon induction. Clin Vaccine Immunol 2007 Jun;14(6):669-77.
          doi: 10.1128/CVI.00042-07pubmed: 17409222google scholar: lookup
        6. Jacks S, Giguère S, Prescott JF. In vivo expression of and cell-mediated immune responses to the plasmid-encoded virulence-associated proteins of Rhodococcus equi in foals. Clin Vaccine Immunol 2007 Apr;14(4):369-74.
          doi: 10.1128/CVI.00448-06pubmed: 17301216google scholar: lookup
        7. Wall DM, Duffy PS, Dupont C, Prescott JF, Meijer WG. Isocitrate lyase activity is required for virulence of the intracellular pathogen Rhodococcus equi. Infect Immun 2005 Oct;73(10):6736-41.
        8. Hooper-McGrevy KE, Wilkie BN, Prescott JF. Immunoglobulin G subisotype responses of pneumonic and healthy, exposed foals and adult horses to Rhodococcus equi virulence-associated proteins. Clin Diagn Lab Immunol 2003 May;10(3):345-51.
        9. Giguère S, Hernandez J, Gaskin J, Prescott JF, Takai S, Miller C. Performance of five serological assays for diagnosis of Rhodococcus equi pneumonia in foals. Clin Diagn Lab Immunol 2003 Mar;10(2):241-5.
        10. Lopez AM, Hines MT, Palmer GH, Alperin DC, Hines SA. Identification of pulmonary T-lymphocyte and serum antibody isotype responses associated with protection against Rhodococcus equi. Clin Diagn Lab Immunol 2002 Nov;9(6):1270-6.
        11. da Silveira BP, Barhoumi R, Bray JM, Cole-Pfeiffer HM, Mabry CJ, Burghardt RC, Cohen ND, Bordin AI. Impact of surface receptors TLR2, CR3, and FcγRIII on Rhodococcus equi phagocytosis and intracellular survival in macrophages. Infect Immun 2024 Jan 16;92(1):e0038323.
          doi: 10.1128/iai.00383-23pubmed: 38018994google scholar: lookup