A study on IL8RB gene polymorphism as a potential immuno-compromised adherent in exaggeration of parenteral and mammo-crine oxidative stress during mastitis in buffalo.

The genetic markers in inflammatory responses during mastitis afford a reasonable way for improving milk production in the Egyptian buffalo breed. Among them is the interleukin 8 Receptor Gene (IL8RB) (CXCR2); a chemokine receptor gene augments the neutrophil migration during infection. To understand its role better during mastitis in Egyptian buffalos, twenty-five dairy animals representing the normal, sub-clinically, clinically and chronically affected buffalos were randomly selected from different districts. Screening criteria for mastitis were based on somatic cell count and California mastitis test assays on their milk samples. Biochemically, mastitis induced an increase in milk lactate dehydrogenase, alkaline phosphatase and catalase activities and serum malanoaldehyde concentration. The total antioxidant concentrations, however, decreased in serum and milk during mammary inflammation. The protein profiling of milk whey proved an accelerated mammary inflammatory influx of blood-borne proteins during mastitis. The genomic DNAs were extracted from blood samples and the CXCR2 sequence of 1246 bp covering a part of intron 1, exon 2 and a part of 3'UTR were submitted to Genbank (accession # KY399457.1). The study clearly defined the presence of four SNPs. Three were detected as synonymous substitutions in coding region and one in the 3'UTR region. Only SNP C/A at c.127 was found to be highly associated with mastitis. In conclusion, the results warrant the potential correlation between the genetic SNP variance for certain genes and the incidence of mastitis in buffalo breed.

Assignment of genes coding for leukocyte surface molecules to river buffalo chromosomes.

A panel of 35 somatic cell hybrids between river buffalo (Bubalus bubalis L.) and Chinese hamster was used in combination with 40 monoclonal antibodies to find synteny among leukocyte antigens and between already established synteny groups and leukocyte antigens. Six synteny groups were identified and three sets of markers were related to already existing synteny groups. Antibody IL-A165 detected CD71, which is syntenic with synteny groups U10 and U25, confirming that U10 and U25 are both are on a biarmed river buffalo chromosome. This would imply that U25 could be assigned to the short arm of the river buffalo chromosome 1 (BBU 1p), as U10 has previously been assigned to this chromosome. Antibodies Buf 32, Buf 24 and BAGB27 detected an antigen syntenic with U1 and U7. This finding suggests that U1, which is assigned to cattle chromosome 16, which corresponds to river buffalo chromosome 5q, is syntenic with U7, and that U7 is located on the short arm of buffalo chromosome 5. Furthermore, the gene coding for CD14 is assigned to U16, which is on cattle chromosome 11 and expected to be on river buffalo chromosome 12.