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The Veterinary record2014; 175(19); 485; doi: 10.1136/vr.102594

Administration of commercial Rhodococcus equi specific hyperimmune plasma results in variable amounts of IgG against pathogenic bacteria in foals.

Abstract: Rhodococcus equi is the most common cause of pneumonia in young foals. A vaccine is not available and the use of R equi-specific hyperimmune plasma (HIP) is common. Despite its widespread use, the efficacy of HIP in preventing disease remains controversial. The objectives of this study were (1) to evaluate the virulence associate protein A (VapA)-specific IgG and IgG subclasses in commercially available R equi HIP and (2) to evaluate serum VapA-specific IgG and IgG subclasses in foals following administration of commercial R equi HIP. Three different lots from four commercial R equi HIP were sampled. VapA-specific IgG and IgG subclasses were evaluated in all samples using an ELISA. Serum was collected from newborn foals either after commercial R equi HIP was administered (n=97) or not (n=70). Serum was also collected from each mare. Administration of HIP significantly (P<0.001) increased VapA-specific IgGs in recipient foals, however, there was a marked variation in VapA-specific IgGs in foals receiving the same product. VapA-specific IgGs were significantly different (P<0.001) between products and varied between lots, with coefficients of variation ranging from 17 to 123 per cent. These results may explain previously reported disparities in HIP efficacy.
Publication Date: 2014-08-12 PubMed ID: 25117301DOI: 10.1136/vr.102594Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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The research investigates the efficiency and variability of antibody response against Rhodococcus equi, a common cause of pneumonia in foals, using commerical hyperimmune plasma (HIP). The study finds that while HIP significantly increases VapA-specific IgGs (antibodies), there is significant variation in results, possibly explaining its controversial effectiveness.

Objective & Methodology

  • The study had two main objectives: to examine the antibodies (VapA-specific IgG and its subclasses) in commercial R equi HIP and to assess these antibodies in foals serum after receiving commercial R equi HIP.
  • Three different batches of four commercial R equi HIP were tested.
  • An ELISA (enzyme-linked immunosorbent assay) was used to evaluate VapA-specific IgG and its subclasses in all the samples.
  • Serum was also collected from newborn foals, both those that had received the commercial R equi HIP (n=97) and those who hadn’t (n=70), and from each of their mothers as well.

Key Findings

  • Administering HIP resulted in a significant increase in VapA-specific IgGs in the foals.
  • However, there was noticeable variability in VapA-specific IgGs among foals, despite them all receiving the same product, indicating high inconsistency in response.
  • The difference in IgGs was significant between HIP products and even varied within different lots of the same product.
  • The variation coefficients ranged from 17 to 123 per cent, demonstrating high disparity.

Conclusion

  • The substantial variation in VapA-specific IgGs in the recipient foals may explain the previously reported inconsistencies in the efficiency of HIP.
  • The researchers suggest further studies to understand the underlying causes of this variability, which could contribute to developing more effective preventive measures against R. equi in the future.

Cite This Article

APA
Sanz MG, Oliveira AF, Page A, Horohov DW. (2014). Administration of commercial Rhodococcus equi specific hyperimmune plasma results in variable amounts of IgG against pathogenic bacteria in foals. Vet Rec, 175(19), 485. https://doi.org/10.1136/vr.102594

Publication

ISSN: 2042-7670
NlmUniqueID: 0031164
Country: England
Language: English
Volume: 175
Issue: 19
Pages: 485

Researcher Affiliations

Sanz, M G
  • Department of Veterinary Science, Maxwell H. Gluck Equine Research Center, Lexington, KY 40546-0099, USA.
Oliveira, A F
  • Department of Veterinary Science, Maxwell H. Gluck Equine Research Center, Lexington, KY 40546-0099, USA.
Page, A
  • Department of Veterinary Science, Maxwell H. Gluck Equine Research Center, Lexington, KY 40546-0099, USA.
Horohov, D W
  • Department of Veterinary Science, Maxwell H. Gluck Equine Research Center, Lexington, KY 40546-0099, USA.

MeSH Terms

  • Animals
  • Animals, Newborn / blood
  • Animals, Newborn / immunology
  • Antibodies, Bacterial / blood
  • Bacterial Proteins / blood
  • Bacterial Proteins / immunology
  • Enzyme-Linked Immunosorbent Assay / veterinary
  • Female
  • Horse Diseases / prevention & control
  • Horses
  • Immunoglobulin G / blood
  • Plasma / immunology
  • Pneumonia, Bacterial / prevention & control
  • Pneumonia, Bacterial / veterinary
  • Rhodococcus equi / immunology
  • Virulence Factors / blood
  • Virulence Factors / immunology

Citations

This article has been cited 8 times.
  1. Rivolta AA, Pittman DC, Kappes AJ, Stancil RK, Kogan C, Sanz MG. The type of anticoagulant used for plasma collection affects in vitro Rhodococcus equi assays. BMC Res Notes 2022 Feb 14;15(1):50.
    doi: 10.1186/s13104-022-05933-4pubmed: 35164828google scholar: lookup
  2. Kahn SK, Cywes-Bentley C, Blodgett GP, Canaday NM, Turner-Garcia CE, Flores-Ahlschwede P, Metcalfe LL, Nevill M, Vinacur M, Sutter PJ, Meyer SC, Bordin AI, Pier GB, Cohen ND. Randomized, controlled trial comparing Rhodococcus equi and poly-N-acetyl glucosamine hyperimmune plasma to prevent R equi pneumonia in foals. J Vet Intern Med 2021 Nov;35(6):2912-2919.
    doi: 10.1111/jvim.16294pubmed: 34738651google scholar: lookup
  3. Kahn SK, Cywes-Bentley C, Blodgett GP, Canaday NM, Turner-Garcia CE, Vinacur M, Cortez-Ramirez SC, Sutter PJ, Meyer SC, Bordin AI, Vlock DR, Pier GB, Cohen ND. Antibody activities in hyperimmune plasma against the Rhodococcus equi virulence -associated protein A or poly-N-acetyl glucosamine are associated with protection of foals against rhodococcal pneumonia. PLoS One 2021;16(8):e0250133.
    doi: 10.1371/journal.pone.0250133pubmed: 34437551google scholar: lookup
  4. Bordin AI, Cohen ND, Giguère S, Bray JM, Berghaus LJ, Scott B, Johnson R, Hook M. Host-directed therapy in foals can enhance functional innate immunity and reduce severity of Rhodococcus equi pneumonia. Sci Rep 2021 Jan 28;11(1):2483.
    doi: 10.1038/s41598-021-82049-ypubmed: 33510265google scholar: lookup
  5. 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
  6. Bujold AR, Lani NR, Sanz MG. Strain-to-strain variation of Rhodococcus equi growth and biofilm formation in vitro. BMC Res Notes 2019 Aug 19;12(1):519.
    doi: 10.1186/s13104-019-4560-1pubmed: 31426832google scholar: lookup
  7. Folmar CN, Cywes-Bentley C, Bordin AI, Rocha JN, Bray JM, Kahn SK, Schuckert AE, Pier GB, Cohen ND. In vitro evaluation of complement deposition and opsonophagocytic killing of Rhodococcus equi mediated by poly-N-acetyl glucosamine hyperimmune plasma compared to commercial plasma products. J Vet Intern Med 2019 May;33(3):1493-1499.
    doi: 10.1111/jvim.15511pubmed: 31034109google scholar: lookup
  8. Trevisani MM, Hanna ES, Oliveira AF, Cardoso SA, Roque-Barreira MC, Soares SG. Vaccination of Mice with Virulence-Associated Protein G (VapG) Antigen Confers Partial Protection against Rhodococcus equi Infection through Induced Humoral Immunity. Front Microbiol 2017;8:857.
    doi: 10.3389/fmicb.2017.00857pubmed: 28553279google scholar: lookup