Antibody isotyping and cytokine profiling in natural cases of Burkholderia mallei infection (glanders) in equines.
Abstract: Immunological aspects of B. mallei infection were rarely studied in natural cases of equines. The present study was conducted to determine IgG, IgM, IgA and IgG (T) titre against recombinant Hcp1, TssA and TssB proteins and PilA-Hcp1-TssN-BipD and BpaB-BpaC- BMAA0553 chimeras and cytokine responses in glanders affected equine serum. Methods: The study was conducted on serum samples collected from 151 glanders positive equines which include horses (n = 134), mules (n = 16), and donkeys (n = 01). The IgM, IgG, IgA and IgG (T) titre were determined against recombinant antigens by indirect ELISA and interleukin(IL)-1β, IL-17, IL-6, tumor necrosis factor alpha(TNF-α), monocyte chemoattractant protein 1 (MCP-1) and interferon gamma (IFN-γ) responses were measured by commercial ELISA kits. Results: The study showed that glanders affected equines elicited strong antibody response against Hcp1, moderate responses against TssA and TssB, and weak responses against two chimeras. Among the cytokines, IL-1β, MCP-1, IL-17 and IL-6 concentration were significantly higher in glanders affected equine serum. Conclusions: We found that IgG antibody titre was higher than IgM, IgG (T) and IgA isotypes and Hcp1 was most predominant antibody inducers in comparison to TssA, TssB, PilA-Hcp1-TssN-BipD and BpaB-BpaC-T2SS proteins. The elevated level of IL-1β, MCP-1, IL-17, IL-6, IFN-γ and TNF-α observed in this study support the important role of this cytokines for augmenting cellular defence by recruitment of macrophages, neutrophil and dendritic cells against B. mallei infection. Further studies should be conducted to determine memory cell responses in natural cases of equine glanders using recombinant B. mallei proteins for identifying well-characterized immuno-protective vaccine candidates.
Copyright © 2024 Elsevier Ltd. All rights reserved.
Publication Date: 2024-11-16 PubMed ID: 39549470DOI: 10.1016/j.cyto.2024.156799Google Scholar: Lookup
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- Journal Article
Summary
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This research investigated the immune responses to the B. mallei infection, glanders, in horses, mules, and donkeys by measuring their antibody and cytokine responses. Antibodies are a type of protein that the immune system produces in response to harmful substances called antigens, while cytokines are small proteins that are key to cellular signaling in the immune response. The study identified high concentrations of specific types of antibodies and cytokines in infected equine serum, which suggests that these play an important role in the combat against B. mallei infection.
Methodology
- For this study, serum samples were taken from 151 equines that were tested positive for glanders, including 134 horses, 16 mules, and 1 donkey.
- Indirect ELISA, a commonly used method to detect specific antibodies, was used to determine IgM, IgG, IgA, and IgG (T) titre against specific recombinant antigens found in B. mallei.
- Commercial ELISA kits were used to measure the concentration of specific cytokines: interleukin(IL)-1β, IL-17, IL-6, tumor necrosis factor alpha(TNF-α), monocyte chemoattractant protein 1 (MCP-1), and interferon gamma (IFN-γ).
Findings
- The study found that glanders-affected equines produced a strong antibody response against one of the measured proteins, Hcp1.
- Moderate responses were found against other proteins, TssA and TssB.
- However, weak responses were detected against two complex proteins, PilA-Hcp1-TssN-BipD and BpaB-BpaC-T2SS.
- Among the studied cytokines, IL-1β, MCP-1, IL-17, and IL-6 concentration were significantly higher in glanders-affected equine serum.
Conclusion
- The results revealed that IgG antibody titre was higher than others, and Hcp1 was the most predominant antibody inducers in comparison to others.
- The study found that the high levels of IL-1β, MCP-1, IL-17, IL-6, IFN-γ, and TNF-α in the serum could contribute to enhancing the cellular defense by recruiting important immune cells against B. mallei infection.
- The researchers recommend further studies to investigate memory cell responses in natural cases of equine glanders using recombinant B. mallei proteins. This will provide valuable insights for the development of effective and well-characterized vaccines against this disease.
Cite This Article
APA
Pooja , Thapa N, Rani R, Shanmugasundaram K, Jhandai P, Rakshita , Bhattacharya TK, Singha H.
(2024).
Antibody isotyping and cytokine profiling in natural cases of Burkholderia mallei infection (glanders) in equines.
Cytokine, 185, 156799.
https://doi.org/10.1016/j.cyto.2024.156799 Publication
Researcher Affiliations
- ICAR- National Research Centre in Equines, Sirsa Road, Hisar, 125001 Haryana, India.
- Griffith College, Dublin Campus, Ireland(1).
- ICAR- National Research Centre in Equines, Sirsa Road, Hisar, 125001 Haryana, India.
- National Centre for Veterinary Type Cultures, ICAR- National Research Centre in Equines, Sirsa Road, Hisar, 125001 Haryana, India.
- ICAR- National Research Centre in Equines, Sirsa Road, Hisar, 125001 Haryana, India.
- ICAR- National Research Centre in Equines, Sirsa Road, Hisar, 125001 Haryana, India.
- ICAR- National Research Centre in Equines, Sirsa Road, Hisar, 125001 Haryana, India.
- ICAR- National Research Centre in Equines, Sirsa Road, Hisar, 125001 Haryana, India. Electronic address: Harisankar.Singha@icar.gov.in.
MeSH Terms
- Animals
- Horses / immunology
- Burkholderia mallei / immunology
- Glanders / immunology
- Glanders / microbiology
- Glanders / blood
- Cytokines / blood
- Horse Diseases / immunology
- Horse Diseases / microbiology
- Horse Diseases / blood
- Antibodies, Bacterial / blood
- Antibodies, Bacterial / immunology
Conflict of Interest Statement
Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Harisankar Singha reports financial support was provided by ICAR-National Research Centre on Equines. Harisankar Singha reports financial support was provided by Indian Council of Agricultural Research (ICAR), New Delhi, India. Harisankar Singha reports financial support was provided by Life Sciences Research Board of Defence Research & Development Organisation (LSRB- DRDO). Harisankar Singha reports a relationship with ICAR- National Research Centre on Equines that includes: employment. If there are other authors, they declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper..
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