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At least 19 recordsLinked to original sources
PubMed1976

Chemical composition and some properties of modified buffalo milk for infant feeding.

A proposed formula for modifying buffalo milk for infant feeding was described. Buffalo milk was diluted with four parts of whey that was produced by addition of citric acid or lemon juice to milk and neutralization with sodium bicarbonate. The chemical composition and the properties of the proposed formula were compared with raw buffalo milk, human milk and buffalo milk modified by the ordinary method. The proposed formula was characterised by low casein/whey protein N comparable to human milk and by curd tension.

Animals↗
PubMed2026

Genomic diversity and resistance determinants of staphylococci from cow and buffalo milk.

BACKGROUND: Staphylococci are important mastitis pathogens in dairy animals and serve as reservoirs of antimicrobial resistance genes (ARGs) having zoonotic potential. Genomic characterization of resistant isolates is essential to understand their diversity, resistance mechanisms, and One Health implications. METHODS AND RESULTS: A total of 363 cow and buffalo milk samples-including 108 from animals with mastitis-were screened, yielding 98 staphylococcal isolates, comprising 20 Staphylococcus aureus and 78 coagulase-negative staphylococci (CoNS). Antimicrobial susceptibility testing revealed resistance to cefoxitin (CoNS: 21.7%; S. aureus: 10%), tetracycline (CoNS: 19.2%; S. aureus: 10%), erythromycin (CoNS:16.7%; S. aureus: 10%), gentamicin (CoNS: 10.2%; S. aureus: 10%) and fluoroquinolone (CoNS: 10.2%), while the majority were sensitive to chloramphenicol, cotrimoxazole (~ 95%, each), linezolid (~ 97%), and vancomycin (100%). Nineteen isolates, including two S. aureus, were cefoxitin-resistant, and eight carried the mecA gene. Whole genome sequencing of these eight isolates revealed genome sizes ranging from 2.27 to 2.78 MB, with the methicillin resistant S. aureus (MRSA, ERSST98) isolate possessing the largest genome and the highest rRNA copy number. Comparative genomic analysis revealed various SCCmec types along with an extensive array of resistance determinants, encompassing aminoglycosides, macrolides, tetracyclines, efflux systems, and heavy metals, underscoring the multifaceted resistance repertoire of these strains. Virulence profiling of ERSST98 demonstrated a broad arsenal of adhesins, toxins, and biofilm‑associated genes, highlighting its pathogenic capacity. Mobile genetic elements with diverse plasmid replicons and insertion sequence families further contributed to genomic plasticity. CONCLUSIONS: Collectively, this study underscores the genomic diversity of methicillin-resistant staphylococci from dairy animals with extensive resistance determinants and highlights their zoonotic relevance within One Health framework.

Animals↗
PubMed1975

Preparation and properties of beta-casein from buffalo's milk.

Beta-casein from individual buffalo's milk was found to be homogeneous by starch-gel electrophoresis. Beta-Casein was separated from buffalo's milk by the method of Warner (1944) and purified by DEAE-cellulose chromatography. Buffalo beta-casein possesses identical end-groups to those of cow beta-casein; namely N-terminal arginine and assuming a single polypeptide chain a possible C-terminal sequence of Ile-Ile-Val. However, the amino-acid composition and the trypic peptide patterns of the 2 proteins are not the same.

Amino Acid Sequence↗
PubMed2026

From buffalo to human: Klebsiella pneumoniae in high-somatic cell count milk as an overlooked link in the one health chain.

High somatic cell count (SCC) is a critical indicator of udder health and milk quality in buffalo milk production. However, in many low-income regions, SCC monitoring is often underemphasized, allowing a proportion of high-SCC buffalo milk to enter the food chain and potentially compromising food safety and public health. Klebsiella pneumoniae (K. pneumoniae) is a common zoonotic pathogen found in high-SCC milk, yet systematic investigations into the prevalence and characteristics in high-SCC buffalo milk remain limited. In this study, 23 K. pneumoniae strains were screened out from 460 bacterial isolates obtained from high-SCC buffalo milk samples from Guangxi, China, with an isolation rate of 5.0%. These isolates were comprehensively characterized using whole-genome sequencing and comparative genomic analyses. The results revealed that 78.26% (18/23) of the isolates shared high genomic similarity with the human reference strain ATCC 13883, and the ST37 clone exhibited a pronounced potential of cross-species transmission. All isolates harbored core adhesion factors and intrinsic resistance genes. Notably, several strains displayed high-risk features: strain 419 carried the K1 capsular serotype, strain 326 possessed a complete yersiniabactin synthesis gene cluster, and strain 320 exhibited a multidrug-resistant phenotype. Phenotypic assays further demonstrated a positive correlation between biofilm formation capacity and virulence in Galleria mellonella. Metabolic pathway enrichment analyses suggested that K. pneumoniae has undergone substantial adaptation to the nutrient-rich buffalo milk environment. Collectively, these findings confirm that raw high-SCC buffalo milk serves as a significant reservoir for high-risk zoonotic K. pneumoniae. While industrial thermal processing effectively eliminates viable pathogens, the resilient antimicrobial resistance determinants within these isolates pose a persistent risk of horizontal gene dissemination along the food chain, providing critical evidence for enhancing pre-processing milk quality regulations within a One Health framework.

Animals↗
PubMed1977

Action of milk clotting enzymes on alphas-caseins from buffalo's and cow's milk.

alphaS-Caseins were isolated from buffalo's and cow's milk and hydrolyzed with rennet, bovine pepsin, microbial proteases from Mucor miebei, Mucor pusillus Lindt, and Endotbia parasitica. The rate of hydrolysis was followed by determining the unaltered alphaS-casein in the digest after acrylamide gel electrophoresis. The rate of hydrolysis of alphaS-casein from the two species with the different enzymes was comparable, being more rapid with microbial enzymes particularly Endotbia parasitica protease. However, the electrophoretic patterns of the degradation products of buffalo's and cow's alphaS-casein produced by microbial rennets were not identical.

Animals↗
PubMed1979

Blood and milk progesterone in pregnant and nonpregnant buffalo.

Changes in progesterone concentration of blood and milk were measured by radioimmunoassay in 10 Murrah buffalo up to 40 days after insemination. Progesterone concentration in blood plasma at estrus was .1 ng/ml which rose to a peak of 3.6 ng/ml on day 13. It continued to increase in animals that conceived but dropped to .6 ng/ml on 3 days before next estrus in those that failed to conceive. The average concentration of progesterone in milk was .5 ng/ml at estrus; it increased to 18 ng/ml on day 15, and thereafter it declined to 4.4 ng/ml 3 days preceding next estrus in nonpregnant animals. In pregnant animals, it was maintained and elevated further to 24.8 ng/ml on day 37. Progesterone in milk was four to five times higher than in blood plasma.

Animals↗
PubMed1979

Stability of buffalo casein micelles.

Buffalo skim-milk is less heat stable than cow skim-milk. Interchanging ultracentrifugal whey (UCW) and milk diffusate with micellar casein caused significant changes in the heat stability of buffalo casein micelles (BCM) and cow casein micelles (CCM). Buffalo UCW dramatically destabilized CCM, whereas buffalo diffusate with CCM exhibited the highest heat stability. Cow kappa-casein stabilizes alphas-casein against precipitation by Ca better than buffalo kappa-casein. About 90% of alphas-casein could be stabilized by kappa:alphas ratios of 0.20 and 0.231 for cow and buffalo, respectively. Sialic acid release from micellar kappa-casein by rennet was higher than from acid kappa-casein in both buffalo and cow caseins, the release being slower in buffalo. The released macropeptide from buffalo kappa-casein was smaller than that from cow kappa-casein as revealed by Sephadex gel filtration. Sub-units of BCM have less sialic acid (1.57 mg/g) than whole micelles (2.70 mg/g). On rennet action, 47% of bound sialic acid was released from sub-units as against 85% from whole micelles. The sub-micelles are less heat stable than whole micelles. Among ions tested, added Ca reduced heat stability more dramatically in whole micelles, whereas added phosphate improved the stability of micelles and, more strikingly, of sub-micelles. Citrate also improved the heat stability of sub-micelles but not of whole micelles.

Animals↗
PubMed1979

Electrophoresis of buffalo (bos bubalis) serum proteins including immunoglobulins.

Antigenic components of buffalo (Bos bubalis) serum, which were also components of buffalo colostrum, seminal plasma, milk whey, saliva, and tears, were investigated by the ager gel diffusion test and immunoelectrophoresis. Immunoglobulins of buffalo serum were identified by immunoelectrophoresis employing rabbit-anti-buffalo serum and rabbit-anti-buffalo gamma-globulin. Based on immunoelectrophoretic patterns immunoglobulin G (IgG), IgGA, and IgM were detected both in the serum and colostrum of buffaloes. Tears contained both IgG and IgM. Cross-reactions of buffalo serum with seminal plasma, saliva, and milk whey were observed only in the IgG region. By polyacrylamide gel electrophoresis, lipoprotein (5.2% +/- 0.41), IgM (11.4% +/- 3.1), IgG (9.4% +/- 0.98), haptoglobin 21.8% +/- 3.73), transferrin (10.4% +/- 2.15), ceruloplasmin (7.8% +/- 1.3), postalbumin (20.8% +/- 2.09), and albumin (13.7% +/- 0.75) were identified provisionally.

Animals↗
PubMed1979

Renal and mammary excretion of sulfadimidine in buffaloes.

The renal and mammary excretion of sulfadimidine was investigated in 8 lactating buffaloes after intravenous administration. The results showed that sulfadimidine was bound to the proteins in plasma (39--59 per cent) and milk (5.5 per cent). The renal handling of sulfadimidine was influenced by the variations in the urinary pH and the concentration of non-protein-bound drug. From the results it is concluded that glomerular filtration, back diffusion and active tubular secretion are involved in the renal handling of sulfadimidine in buffaloes. The results of mammary excretion showed that sulfadimidine is excreted into milk of buffaloes in concentration lower than in plasma. The ratio between the concentration of sulfadimidine in milk and plasma increases when the pH of milk increases. The results are consistant with the theory that drugs are excreted through the mammary gland by passive diffusion.

Animals↗
PubMedDate not supplied

The primary structure of the beta-lactoglobulin of the waterbuffalo (Bubalus arnee).

The complete amino acid sequence of the beta-lactoglobuline of the waterbuffalo (Bubalus arnee) was established. The sequence of peptides obtained by cleavage with BNPS-Skatole, CNBr and trypsin were determined automatically by the help of the sequenator. Only two differences were found in the beta lactoglobulin of the waterbuffalo compared with the bovine beta-lactoglobulin B.

Amino Acid Sequence↗