Fernando N. Souza

Function of milk polymorphonuclear neutrophil leukocytes in bovine mammary glands infected with Corynebacterium bovis

Corynebacterium bovis is one of the most commonly isolated bacteria from aseptically collected bovine milk samples. The objective of the current study was to characterize the bovine innate immune response by evaluating milk polymorphonuclear neutrophilic leukocytes (PMNL) in mammary glands infected with C. bovis. Twenty quarters infected with C. bovis and 28 culture-negative quarters (with milk somatic cell count <1×10(5) cells/mL) were used. The percentages of milk PMNL and the PMNL expression of L-selectin (CD62L), β2-integrin (CD11b), and one of the endothelial-selectin ligands (CD44), as well as the levels of intracellular reactive oxygen species (ROS) and the phagocytosis of Staphylococcus aureus, were evaluated by flow cytometry. The apoptosis and necrosis rates of the PMNL were quantified using dual-color flow cytometry with fluorescein-labeled annexin and propidium iodide. The present study revealed a higher percentage of PMNL in the milk from C. bovis-infected quarters, although no significant differences were found in levels of CD44, CD62L, or CD11b expression among the PMNL. A lower percentage of apoptotic PMNL was observed in C. bovis-infected quarters, as well as higher percentages of viable PMNL and of PMNL that produced intracellular ROS. However, no alterations were observed in phagocytosis of Staph. aureus by the PMNL or in intensity of intracellular ROS production by PMNL. Thus, results from this investigation of the PMNL function support, at least in part, the fact that intramammary infections by C. bovis may offer protection against intramammary infections by other bacteria.

Effects of bovine leukemia virus infection on milk neutrophil function and the milk lymphocyte profile

The effects of bovine leukemia virus (BLV) on the immune response have been extensively investigated; however, its effects on mammary gland immunity are only speculative. Although BLV has a tropism for B cells, it can affect both adaptive and innate immunities because these systems share many effector mechanisms. This scenario is the basis of this investigation of the effects of BLV on mammary gland immunity, which is largely dependent upon neutrophilic functions. Thus, the present study sought to examine neutrophilic functions and the lymphocyte profile in the milk of naturally BLV-infected cows. The viability of the milk neutrophils and the percentage of milk neutrophils that produced reactive oxygen species (ROS) or phagocytosed Staphylococcus aureus were similar between BLV-infected and BLV-uninfected dairy cows. Furthermore, the expression of CD62L and CD11b by the milk neutrophils and the percentage of milk neutrophils (CH138+ cells) that were obtained from the udder quarters of the BLV-infected cows were not altered. Conversely, the median fluorescence intensity (MFI) representing intracellular ROS production and the phagocytosis of S. aureus, the expression of CD44 by the milk neutrophils and the percentage of apoptotic B cells were lower in the milk cells from BLV-infected dairy cows, particularly those from animals with persistent lymphocytosis (PL). The lymphocyte subsets were not different among the groups, with the exception of the percentage of CD5−/CD11b− B cells, which was higher in the milk cells from BLV-infected cows, particularly those with PL. Thus, the present study provides novel insight into the implications of BLV infection for mammary gland immunity.

The neutrophil function and lymphocyte profile of milk from bovine mammary glands infected with Streptococcus dysgalactiae

Streptococcus dysgalactiae is a bacterium that accounts for a notable proportion of both clinical and subclinical intramammary infections (IMIs). Thus, the present study explores the function of milk neutrophils and the lymphocyte profile in mammary glands naturally infected with Streptococcus dysgalactiae. Here, we used 32 culture-negative control quarters from eight clinically healthy dairy cows with low somatic cell counts and 13 S. dysgalactiae-infected quarters from six dairy cows. Using flow cytometry, we evaluated the percentage of milk monocytes/macrophages and neutrophils, expression of CD62L, CD11b and CD44 by milk neutrophils, the levels of intracellular reactive oxygen species (ROS) production and phagocytosis of Staphylococcus aureus by milk neutrophils, and neutrophil viability. Furthermore, the percentages of B cell (CD21(+)) and T lymphocyte subsets (CD3(+)/CD4(+)/CD8(-); CD3(+)/CD8(+)/CD4(-); and CD3(+)/CD8(-)/CD4(-)), and the expression of CD25 by T milk lymphocytes (CD3(+)) and T CD4(+) milk cells were also assessed by flow cytometry using monoclonal antibodies. The present study showed a higher SCC and percentage of milk neutrophils, and a decrease in the percentage of milk monocytes/macrophages from S. dysgalactiae-infected quarters when compared to uninfected ones. We also observed a higher expression of CD11b by milk neutrophils and a tendency toward a decrease in neutrophil apoptosis rate in S. dysgalactiae-infected quarters. In addition, the S. dysgalactiae-infected quarters had higher percentages of milk T cells (CD3(+)) and their subset CD3(+)CD8(+)CD4(-) cells. Overall, the present study provided new insights into S. dysgalactiae IMIs, including distinct lymphocyte profiles, and a tendency toward an inhibition of apoptosis in milk neutrophils.

Viabilidade celular, fagocitose e espraiamento de fagócitos mononucleares, e liberação de peróxido de hidrogênio por leucócitos de glândulas mamárias bovinas sadias e infectadas

The study aimed to evaluate the cell viability, the phagocytosis and spreading rates by the mononuclear phagocytes, and hydrogen peroxide (H2O2) release by leukocytes from healthy and infected mammary glands. Thus, 94 milk samples were divided according the results of the bacteriological analysis and the somatic cell count (SCC). No significant difference was found in cell viability, the phagocytosis and spreading rates by mononuclear phagocytes between the distinct groups. Therefore, the H2O2 release by leukocytes was higher in the milk samples from healthy mammary glands compared to those infected with Streptococcus spp. or Corynebacterium spp. However, when the H2O2 release by phagocytes in 1mL of milk according to SCC mL-1 of each sample was estimated, it was found that milk samples from infected, infected with Staphylococcus spp. and bacteriological negative quarters with high SCC were higher than the healthy ones. It was also observed a positive correlation among SCC and cell viability or phagocytosis and spreading rates, and a negative correlation between H2O2 release and cell viability or SCC. In face of, it can be concluded that the SCC, as well as their function and the cell viability, are related to mammary gland health.

Flow cytometric analysis: Interdependence of healthy and infected udder quarters

An important question about intramammary infections that is still debated in the literature is the independence or interdependence of the quarters of dairy cows. The present study sought to explore milk neutrophil function and the milk lymphocyte profile of uninfected quarters from uninfected and infected (one infected quarter per cow) udders to evaluate interdependence of the quarters. Thus, 32 (8 cows) and 18 (6 cows) uninfected quarters from uninfected and infected udders were used, respectively. Using flow cytometry, we evaluated the percentage of milk neutrophils and their expression of adhesion molecules L-selectin (CD62L), β2-integrin (CD11b), and an endothelial-selectin ligand (CD44); levels of intracellular reactive oxygen species (ROS); phagocytosis of Staphylococcus aureus by milk neutrophils; and neutrophil viability. Furthermore, we assessed the percentage of B-cell (CD21(+)) and T-lymphocyte subsets (CD3(+)/CD4(+)/CD8(-), CD3(+)/CD8(+)/CD4(-), CD3(+)/CD4(+)/CD25(-), CD3(+)/CD4(+)/CD25(+), and CD3(+)/CD4(-)/CD25(-)) using flow cytometry with monoclonal antibodies. The infected quarter did not affect somatic cell count or the percentage of neutrophils in the neighboring uninfected quarters. Furthermore, the infected quarter did not influence neutrophil viability, intracellular reactive oxygen species production, or phagocytosis of S. aureus by milk neutrophils. Conversely, the expression of adhesion molecules CD11b, CD62L, and CD44 by milk neutrophils differed between uninfected quarters from infected versus uninfected udders. The lymphocyte subsets did not differ between groups, except for a higher percentage of B cells in uninfected quarters from infected udders than in those from uninfected udders. Thus, our study strongly supports the hypothesis of interdependence of quarters based on the influence of infection on both the percentage of B cells and the expression of adhesion molecules by milk neutrophils in the neighboring uninfected quarters.

Influence of race and crossbreeding on casein micelles size

Casein (CN) micelles are colloidal aggregates of protein dispersed in milk, the importance of which in the dairy industry is related to functionality and yield in dairy products. The objective of this work was to investigate the correlation of milk CN micelles diameter from Holstein and Zebu crossbreds with milk composition (protein, fat, lactose, total and nonfat solids and milk urea nitrogen), somatic cell count (SCC), age, lactation stage and production. Average casein micelles diameters of milk samples obtained from 200 cows were measured using photon correlation spectroscopy and multiple regression analysis was used to find relationship between variables. CN micelle diameter, SCC and nonfat solids were different between animals with different Holstein crossbreed ratios, which suggests influence of genetic factors, mammary gland health and milk composition. Overall, results indicate the potential use of CN micelle diameter as a tool to select animals to produce milk more suitable to cheese production.

Clinical findings related to intramammary infections in meat-producing ewes.

The aim of this study was to investigate the relationship between clinical findings and bacterial isolation in milk samples of meat-producing ewes. The study was conducted in 17 commercial flocks and 550 udder halves from suckling Santa Ines ewes. Initially, the clinical examination of the mammary glands and teats was performed by visual inspection and palpation of the teats and udder halves; then a scoring system was devised for all the findings. After that, the strip cup test and the California mastitis test (CMT) were performed. Then, milk samples for somatic cell counts (SCCs) and bacteriological analyses were collected. Staphylococci bacteria were the main etiological agent isolated in the present study. Upon investigation of the correlations between bacterial isolation and the clinical findings, only the presence of teat injury, pendulous udder, and alterations in the palpation of the teat were associated with bacterial isolation. A significant correlation between bacteriologically positive milk samples and CMT and SCC was also found. Thus, some clinical findings appeared as a risk factor for bacteriologically positive milk samples and can be used as a tool in mastitis control programs. However, a complete and extensive diagnosis, an appropriate therapy, and an efficient mastitis control program will require the combination of clinical examination, microbiological tests, and SCC.

Variações metodológicas na contagem de células somáticas do leite de ovelhas da raça Santa Inês

The present study was designed to assess the correlation among the automatic somatic cell count and the microscopic somatic cell count using the Broadhurst-Paley (BP), Hematoxilin-eosin (HE) and Rosenfeld dyes. The milk smears were stained with BP, HE and Rosenfeld and the automatic cell count was performed by flow cytometry. The mean logarithmic microscopic SCC by BP and Rosenfeld was higher than the values from automatic SCC and microscopic SCC by HE (P<0.0001). Indeed, the mean values from microscopic SCC using the HE was lower than the automatic cell count (P<0.0001). The correlation among the automatic cell count and the microscopic SCC using the HE, BP and Rosenfeld dyes were 0.774, 0.803 e 0.859 (P<0.0001), respectively. The automatic SCC values and the estimated automatic SCC applying the quadratic equation using the results of the microscopic SCC using the HE (P=0.90), BP (P=0.09) and Rosenfeld (P=0.23) dyes were not different. Thus, it can be concluded that the SCC was influenced by the methodology applied, and nonspecific stains used for microscopic SCC can be used to assess udder health in ewes if an equation is applied to estimate automatic SCC.

Correlação entre a contagem automática de células somáticas e a porcentagem de neutrófilos pela citometria de fluxo e pela técnica de citocentrifugação

The purpose of the present study was to assess the correlation between the automatic somatic cell count (SCC) and the percentage of neutrophils through cytocentrifugation technique and flow cytometry. Thus, 102 milk samples from 28 Holstein dairy cows were collected and submitted to milk cell isolation procedures, and afterwards, the neutrophils were identified. After cytocentrigugation, the neutrophils were microscopically identified using the rosenfeld dye. The milk neutrophils were recognized by flow cytometry using primary mouse IgM monoclonal antibody (CH138A) and phycoerytrin (PE) goat anti-mouse IgM antibody. This study found a positive correlation between SCC and the percentage of neutrophils through cytocentrifugation (r= 0.267) and flow cytometry (r= 0.625). A positive correlation was also encountered between the percentage of neutrophils through cytocentrifugation and flow cytometry (r= 0.496), although the percentage of neutrophils was higher in samples submitted to cytocentrifugation. In conclusion, flow cytometry can be a useful tool in the diagnosis and control of mastitis.

Resíduos de piretróides, lactonas macrocíclicas e antimicrobianos em amostras de leite de tanque no estado de Minas Gerais

Picinin L.C.A., Toaldo I.M., Hoff R.B., Souza F.N., Leite M.O., Fonseca L.M., Diniz S.A., Silva M.X., Cerqueira M.M.O.P. & Bordignon-Luiz M.T. 2017. Survey of pyrethroid, macrocyclic lactone and antibacterial residues in bulk milk tank in Minas Gerais State, Brazil. Pesquisa Veterinária Brasileira 37(2):97-104. Departamento de Ciência e Tecnologia de Alimentos, Universidade Federal de Santa Catarina, Rodovia Admar Gonzaga 1346, Bairro Itacorubi, Florianópolis, SC 88034-001, Brazil. E-mail: lidia.picinin@gmail.com A survey of veterinary drug residues in bulk milk tank from Minas Gerais State, Brazil, was carried out through a broad scope analysis. Here, 132 raw milk samples were collected at 45 dairy farms in Minas Gerais from August 2009 to February 2010, and analyzed for 42 analytes, comprising pyrethroids, macrocyclic lactones and antibacterials, using liquid chromatography coupled with mass spectrometry in tandem mode and gas chromatography with electron capture detection. Within all milk samples, at least one veterinary drug residue was identified in 40 milk samples (30.30%) by confirmatory tests, whereas 16 samples (12.12%) showed the presence of at least two residues. With regard to the Brazilian maximum residue levels, 11 milk samples (8.33%) were non-compliant according to Brazilian Legislation. The veterinary drugs detected in the non-compliant milk samples include penicillin V (one sample), abamectin (one sample) and cypermethrin (nine samples). Furthermore, the antibacterial screening methods failed to identify most of the positive samples that were detected by confirmatory tests, leading to a large discrepancy between the screening and confirmatory antimicrobial tests. Thus, the present study indicated that the veterinary drugs residues still represents a great concern for the milk production chain. INDEX-TERMS: Veterinary drug, pesticide, anthelmintic, antibiotic, raw milk. 1 Received on June 24, 2016. Accepted for publication on July 13, 2016. Part of the L.C.A. Picinin Doctoral thesis in Food Science, Universidade Federal de Santa Catarina, Florianópolis, Brazil. 2 Departamento de Ciência e Tecnologia de Alimentos, Universidade Federal de Santa Catarina (UFSC), Rodovia Admar Gonzaga 1346, Bairro Itacorubi, Florianópolis, SC 88034-001, Brazil. 3 Departamento de Produção Animal e Alimentos, Centro de Ciências Agroveterinárias, Universidade do Estado de Santa Catarina, Lages, SC 88520-000, Brazil. *Corresponding author: lidia.picinin@gmail.com 4 Laboratório Nacional Agropecuário (Lanagro), Ministério da Agricultura, Pecuária e Abastecimento, Porto Alegre, RS 91780-580, Brazil. 5 Departamento de Tecnologia e Inspeção de Produtos de Origem Animal, Escola de Medicina Veterinária, Universidade Federal de Minas Gerais (UFMG), Belo Horizonte, MG 31270-901, Brazil. 6 Departamento de Medicina Veterinária Preventiva, Escola de Medicina Veterinária, UFMG, Belo Horizonte, MG 31270-901, Brazil.