In‐depth immunophenotyping reveals significant alteration of lymphocytes in buffalo with brucellosis

Author:

Grandoni Francesco1ORCID,Signorelli Federica1,Martucciello Alessandra2,Napolitano Francesco1,De Donato Immacolata2,Donniacuo Anna2,Di Vuolo Gabriele2,De Matteis Giovanna1ORCID,Del Zotto Genny3ORCID,Davis William C.4,De Carlo Esterina2

Affiliation:

1. CREA‐Consiglio per la Ricerca in Agricoltura e l'Analisi dell'Economia Agraria Centro di ricerca Zootecnia e Acquacoltura (Research Centre for Animal Production and Aquaculture) Monterotondo Italy

2. Istituto Zooprofilattico Sperimentale del Mezzogiorno National Reference Centre for Hygiene and Technologies of Water Buffalo Farming and Productions Salerno Italy

3. Dipartimento Integrato dei Servizi e Laboratori U.O.C. Laboratorio Analisi, IRCCS Istituto Giannina Gaslini Genoa Italy

4. Department of Veterinary Microbiology and Pathology Washington State University Pullman Washington USA

Abstract

AbstractWater buffalo (Bubalus bubalis) has a prominent position in the livestock industry worldwide but still suffers from limited knowledge on the mechanisms regulating the immune against infections, including brucellosis (BRC), one of the most significant neglected zoonotic diseases of livestock. Seventy‐three buffalo were recruited for the study. Thirty‐five were naturally infected withBrucella spp. The aims of the study were to (i) verify the cross‐reactivity of 16 monoclonal antibodies (mAbs) developed against human, bovine, and ovine antigens; (ii) evaluate lymphocyte subset alterations in BRC positive buffalo; (iii) evaluate the use of the canonical discriminant analysis (CDA), with flow cytometric data, to discriminate BRC positive from negative animals. A new set of eight mAbs (anti CD3e, CD16, CD18, CD45R0, CD79a; CD172a) were shown to cross‐react with water buffalo orthologous molecules. BRC positive animals presented a significant (p < 0.0001) decrease in the percentage of PBMC (29.5 vs. 40.3), total, T and B lymphocytes (23.0 vs. 35.5, 19.2 vs. 28.9, 2.6 vs. 5.7, respectively). In contrast, they showed an increase in percentage of granulocytes (65.2 vs. 55.1;p < 0.0001) and B lymphocytes CD21neg(22.9 vs. 16.1;p = 0.0067), a higher T/B lymphocyte ratio (10.3 vs. 6.4;p = 0.0011) and CD3+/CD21+(14.7 vs. 8.3;p = 0.0005) ratio. The CDA, applied to 33 different flow cytometric traits, allowed the discrimination of all BRC positive from negative buffalo. Although this is a preliminary study, our results show that flow cytometry can be used in a wide range of applications in livestock diseases, including in support of uncertain BRC diagnoses.

Funder

Ministry of Health

Publisher

Wiley

Subject

Cell Biology,Histology,Pathology and Forensic Medicine

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