The discovery of electrophoretically distinct types of β-lactoglobulin (β-lg) by Aschaffenburg & Drewry (Reference Aschaffenburg and Drewry1955) initiated the beginning of extensive investigations of the different genotypes of this whey protein (Hambling et al. Reference Hambling, McAlpine, Sawyer and Fox1992). The two main genetic forms of β-lg differ in the substitution of a Gly and an Ala in the B variant, for an Asp and a Val in the A variant (Ghashghaei, Reference Ghashghaei2003) and this slight molecular difference has been widely associated with significant differences in milk composition in dairy cows (Dove, Reference Dove, Mol and Clegg2000).
Several studies have reported the association of significantly higher fat content (Ng Kwai-Hang et al. Reference Ng Kwai-Hang, Hayes, Moxley and Monardes1986; Aleandri et al. Reference Aleandri, Buttazzoni, Schneider, Caroli and Davoli1990; Tsiaras et al. Reference Tsiaras, Bargouli, Banos and Boscos2005), protein (Litwinczuk et al. Reference Litwinczuk, Barlowska, Krol and Litwinczuk2006), casein (Robitaille et al. Reference Robitaille, Britten, Morisset and Petitclerc2002), true protein (Bobe et al. Reference Bobe, Beitz, Freeman and Lindberg1999) and total solids (Celik, Reference Celik2003) with BB variant, while others have found higher milk component concentrations due to the AA variant (Ng Kwai-Hang et al. Reference Ng Kwai-Hang, Otter, Lowe, Boland and Auldist2002b; Robitaille et al. Reference Robitaille, Britten, Morisset and Petitclerc2002; Molina et al. Reference Molina, Kramm, Brito, Carrillo, Pinto and Ferrando2006). Nonetheless, some authors have found no relationship between β-lg polymorphism and milk composition, and attributed the differences observed in fat and protein contents to other factors (Ng Kwai-Hang et al. Reference Ng Kwai-Hang, Dodds, Boland and Auldist2002a).
Factors other than genetic polymorphism of milk proteins, e.g., seasonal variations (Paquin & Lacroix, Reference Paquin and Lacroix1994; Carlsson et al. Reference Carlsson, Bergstrom and Pehrson1995; Lacroix et al. Reference Lacroix, Verret and Paquin1996; Allore et al. Reference Allore, Oltenacu and Erb1997; Auldist et al. Reference Auldist, Walsh and Thomson1998; Sharma et al. Reference Sharma, Kumar and Pathak2002; Lindmark-Mänsson et al. Reference Lindmark-Mänsson, Fonden and Pettersson2003; Teixeira et al. Reference Teixeira, Freitas and Barra2003; Amenu et al. Reference Amenu, Cowan, Deeth and Moss2006) and breed (Auldist et al. Reference Auldist, Walsh and Thomson1998; Arunvipas et al. Reference Arunvipas, Dohoo, Van Leeuwen and Keefe2003) all affect milk composition but their interaction with β-lg genetic variants has not been studied. Moreover, data on the association between β-lg genetic variants of Girolando cows and milk composition of this breed are still rare. The Girolando breed is basically the result of crossing between the Holstein and Gir (indigenous Zebu breed) in standard proportions of 3/8 Zebu and 5/8 Taurine. This crossbred breed is very common in Brazil because it is claimed to have both the high resistance to heat and humidity characteristic of Indian cattle and the high productivity characteristic of European cattle (Bicalho et al. Reference Bicalho, Pimenta, Mendes, Pena, Queiroz and Pena2006). The objective of this study was to evaluate the effect of genetic polymorphism of β-lg on milk composition (fat, lactose, total solids, milk urea nitrogen, total protein, true protein, casein and somatic cell counts) in Holstein and Girolando cows, during dry and rainy seasons.
Material and Methods
Selection of herds and cows for sampling
The study was carried out in eleven commercial dairy herds in the state of São Paulo, Brazil; among them six were composed of Girolando (crossbred Holstein-Zebu) and five of Holstein cows. Milk and blood samples were taken from 278 lactating Holstein cows and 156 lactating Girolando cows during two dry seasons and two rainy seasons (Sampling period 1, September and October, 2003; Sampling period 2, June and July, 2004; Sampling period 3, November and December, 2004; and Sampling period 4, January and February, 2005). In each dairy herd, the sampled cows had to fulfil the following criteria: first–third lactation and 30–250 d of lactation. Cows with clinical mastitis, or submitted to mastitis treatment 2 weeks before milk sampling, were excluded from this study. In addition, at the time of milk sampling, information such as age, days in lactation and type of feeding system (pasture, supplemented pasture or total mixed ration) for each selected dairy cow was registered.
Milk samples were collected during morning milking in order to represent the whole milking of each animal. The individual samples were collected directly from the collection bucket immediately after milking, or during milking, using flux measurement devices connected to the milk line. Collected samples were split into two flasks: one treated with Bronopol (Boots Microcheck, Nottingham, UK) was used for fat, lactose, total solids, milk urea nitrogen and somatic cell determinations; and the other was used for analysis of milk protein fractions.
Methods of analysis
Milk composition:
Milk samples were analysed for fat, lactose and total solids by infrared absorption methodology (Bentley 2000, Bentley, Chasca MN, USA). Milk urea nitrogen (MUN) was determined by the colorimetric-enzymic method (Chemspec 150, Bentley Instruments Inc., Chasca MN, USA). Somatic cells were electronically counted (Somacount 300, Bentley Instruments Inc.) and converted to log scale (LogSCC). Milk protein fractions were determined for total nitrogen (AOAC, 1990; method 33.2.11; 991·20), non-casein nitrogen (NCN) (Lynch et al. Reference Lynch, Barbano and Fleming1998) and non-protein nitrogen (NPN) (AOAC, 1995; method 33.2.12; 991·21). In order to express the results as total protein (TP), total nitrogen values found were multiplied by 6·38 (Barbano et al. Reference Barbano, Clark, Dunham and Fleming1990). Milk true protein (MTP) and casein concentrations were obtained by difference according to: TP−(NPN×6·38)=milk true protein, and MTP−(NNC×6·38)=casein, respectively.
β-lg genetic polymorphism analysis:
After DNA extraction from blood samples according to Ciulla et al. (Reference Ciulla, Sklar and Hauser1988), extracted DNA samples were submitted to PCR amplification as described by Schlee & Rottmann (Reference Schlee and Rottmann1992). The oligonucleotides primers used for DNA amplification were synthesized by Invitrogen Custom Primers (Inivitrogen Corp., Carlsbad CA 92008, USA), according to the sequence described by Faria et al. (Reference Faria, Guimarães, Mourão, Lima and Pinheiro2000) :
Forward: 5′ACCTGGAGATCCTGCTGCAGAAATG3′
Reverse: 5′CATCGATCTTGAACACCGCAGGGAT3′
Each amplification reaction consisted of PCR buffer 1X (500 mm-KCl, 100 mm-Tris–Cl pH 8·3), 0·1 μl of the described primers, 2·0 μl dNTP (0·125 mm), 0·1 μl Taq polymerase (Cenbiot/RS, PHN/MG), 0·75 μl MgCl2 (Cenbiot/RS, PHN/MG), 5·0 μl of DNA and mili-Q water qsp 25 μl. In all amplified reactions, a control (blank/no-DNA) was used to confirm the absence of contamination during the analysis. The amplification process was carried on a PTC 100-MJ Research thermocycler (MJ Research Inc., Watertown MA 02472, USA).
After DNA amplification of the targetted fragment, a 961-bp region of the β-lg gene, the PCR product (20 μl) was submitted to RFLP in a 2% agarose gel electrophoresis, and digested by the restriction enzyme Hph-I (Invitrogen Corp.) according to Wilkins & Kuys (Reference Wilkins and Kuys1992) to show the presence of either AA, AB or BB genotypes. Hph-I cleaved amplified fragments in 741 and 220 bp (AA genotype), 741, 166 and 54 bp (BB genotype), or a combination of both (AB genotype), with 741, 220, 166 and 54 bp (Wilkins & Kuys, Reference Wilkins and Kuys1992). After β-lg gene identification, the genotype and allele frequencies for the studied herd were obtained.
Statistical analysis
Effects of β-lg, breed and seasonality were analysed in a randomized block design with number of lactation (1, 2 and ⩾3) and feeding system (pasture, supplemented pasture or total mixed ration) as blocks. For statistical analysis, selected cows were distributed according to the β-lg genetic variant (AA, AB or BB), breed (Holstein or Girolando) and seasonality (dry or rainy season). Descriptive statistics of the given results were stored (arithmetic mean and sem) and analysis of variance was performed, evaluating the effects of breed, seasonality and genetic variation of β-lg on the response variables, by the SAS PROC GLM procedure (Statistical Analysis System, Version 8.02; SAS Institute Inc., Cary NC 2001, USA).
In the adopted model, dependent variables used were milk composition (MC) characteristics and fixed factors were β-lg polymorphism, breed and seasonality. The model is described as follows:
MC is the variable considered for milk composition; μ=mean value for the characteristic; Li=lactation number (i=1, 2 and ⩾3), Fj=feeding system (j=pasture, supplemented pasture or total mixed ration), Bl=Breed (l=Holstein and Girolando); Pm=genotypes (m=AA, AB and BB); Sn=seasonality (n=rainy and dry season); eijlmnp=error.
Results
Genetic polymorphism of β-lg in Holstein and Girolando cows
A total of 278 Holstein and 156 Girolando cows were tested for genetic polymorphism of β-lg. The distribution of genotype and allele frequencies for the β-lg gene of Holstein and Girolando cows, obtained by PCR-RFLP, is summarized in Table 1.
Table 1. β-lactoglobulin gene and allele frequencies for Holstein and Girolando cows
† sem according to Oner & Elmaci (Reference Oner and Elmaci2006)
All three β-lg genotypes (AA, AB and BB) were present in both breeds. The allele B was present in a higher frequency both for Holstein and Girolando breed (0·5305±0·021 and 0·6185±0·027, respectively). The frequency of appearance of genotypes differed between Holstein and Girolando cows. BB genotype was the most frequent (38·85% and 44·87%) among studied breeds. AA and AB genotypes had frequencies of 32·73% and 28·42% for Holstein, but 21·15% and 33·97% for Girolando cows.
Effect of β-lg genetic polymorphism and breed on milk composition
Milk composition mean values and sem for β-lg genotypes in Holstein and Girolando cows are shown in Table 2.
Table 2. Effect of β-lactoglobulin polymorphism in Holstein and Girolando cows on milk composition
No statistical differences in milk composition of both breeds were observed among β-lg genotypes for any of the studied variables except for milk urea nitrogen concentration, which was higher (16·64 mg/dl) for Holstein than for Girolando cows (14·38 mg/dl). No interaction between β-lg and breed was found for milk composition.
The average of milk fat and total solids content for the AA, AB and BB genotypes did not differ in any of the breeds. For Holstein cows, milk fat averages were 3·305, 3·267 and 3·359% for the AA, AB and BB genotypes, respectively, while for Girolando, the averages were 3·143, 3·274 and 3·166% for the same genotypes. Total solids averages 11·824, 11·823 and 11·876% among Holstein cows of AA, AB and BB genotypes, respectively, and 11·595, 11·808 and 11·755%, respectively to the cited genotypes for Girolando animals.
Concentrations of total protein, true protein, casein, MUN as well the casein:true protein ratio were not influenced by the β-lg genotypes in this study. Milk from Holstein and Girolando BB cows, respectively, had total protein of 3·125 and 3·091%, true protein of 2·892 and 2·859%, and casein of 2·095 and 2·070%. Averages for the casein:true protein ratio among BB genotype cows were 0·722 for the Holstein breed and 0·721 for Girolando.
Effect of β-lg genetic polymorphism and seasonality on milk composition
Effects of seasonality and β-lg polymorphism on milk composition are shown on Table 3.
Table 3. Effect of seasonality and β-lactoglobulin polymorphism on milk composition
Concentrations of lactose, MTP, casein and casein:MTP ratio were significantly higher during the dry season than in the rainy season. Average concentrations for the dry season were 4·501, 2·918 and 2·132 g/100 g of milk, respectively for lactose, TP, MTP and casein, while rainy season corresponding means were 4·349, 2·846 and 1·994 g/100 g of milk. No interaction between seasonality and β-lg polymorphism was observed.
When non-significant interactions were removed from the statistical model, casein concentrations observed during the rainy season were different among β-lg genetic variants (AA>BB) with higher averages for AA (2·067 g/100 g of milk) compared with BB cows (1·949 g/100 g of milk). But no differences were observed for milk composition variables among β-lg variants within the dry season.
Discussion
Ng Kwai-Hang et al. (Reference Ng Kwai-Hang, Hayes, Moxley and Monardes1986), Van Eenennaam & Medrano, (Reference Van Eenennaam and Medrano1991), Celik (Reference Celik2003), Oner & Elmaci (Reference Oner and Elmaci2006) reported higher frequencies for the B allele for Holstein cows. In the present study, the frequency of genotype appearance differed between Holstein and Girolando cows. Although the BB genotype was the most frequent for both breeds (38·85% and 44·87%), AA genotype was the second higher in frequency level in Holstein breed (BB>AA>AB), while the AB was more frequent than AA genotype in Girolando cows (BB>AB>AA). Higher levels of BB genotype frequencies among Holstein cows were also observed by Celik (Reference Celik2003) but not by Hill (Reference Hill1993) and Oner & Elmaci (Reference Oner and Elmaci2006), who found a higher number of the heterozygous AB variants compared with homozygous cows.
Nevertheless, no report on β-lg genetic variants in Girolando animals was found in the literature, and data on β-lg allele frequency among Bos indicus breeds show a higher prevalence for the B gene (Silva & Del Lama, Reference Silva and Del Lama1997; Neves et al. Reference Neves, Guimarães, Lima, Penna and Pinheiro1998; Faria et al. Reference Faria, Guimarães, Mourão, Lima and Pinheiro2000) and a higher frequency for the BB genotype.
The present results differ from those of Ng Kwai-Hang et al. (Reference Ng Kwai-Hang, Hayes, Moxley and Monardes1986), Aleandri et al. (Reference Aleandri, Buttazzoni, Schneider, Caroli and Davoli1990), Bovenhuis et al. (Reference Bovenhuis, Arendonk and Korver1992) and Hill (Reference Hill1993). These authors all reported higher milk fat concentration in milk of Holstein cows comprising B variants of β-lg, and Hill (Reference Hill1993) concurred for significantly lower concentrations of fat and total solids in AA Holstein milk.
Milk nitrogen fractions were not influenced by β-lg genetic polymorphism in any of the breeds, although TP, MTP, casein means and casein:MTP ratio for AA cows were numerically higher for both breeds. Similarly, Molina et al. (Reference Molina, Kramm, Brito, Carrillo, Pinto and Ferrando2006) and Bobe et al. (Reference Bobe, Beitz, Freeman and Lindberg1999) found an increase in TP concentrations of milk when B allele was substituted for A. According to Bobe et al. (Reference Bobe, Beitz, Freeman and Lindberg1999) such increment is due to the higher percentage of casein in β-lg A milk, while Molina et al. (Reference Molina, Kramm, Brito, Carrillo, Pinto and Ferrando2006) attributed this increase to the higher content of whey protein in milk with A variants. Mean values for casein and MTP concentrations in the present study, however, seem to be in disagreement with Robitaille et al. (Reference Robitaille, Britten, Morisset and Petitclerc2002), who found a tendency for higher casein concentrations in BB β-lg milk in Holsteins, and with a report of increased MTP when B allele was more frequent in the Holstein breed (Ng Kwai-Hang, Monardes & Hayes, Reference Ng Kwai-Hang, Monardes and Hayes1990).
Although not statistically significant, the casein: MTP ratios for AA milk of both breeds were slightly higher than those observed for either AB or BB genotypes, and this is particularly relevant as MTP, especially β-lg concentrations in milk true protein, plays an important role in milk stability during heat treatment, since this protein strongly interacts with other milk molecules, particularly κ-casein (Karatzas & Turner, Reference Karatzas and Turner1997; Fox & McSweeney, Reference Fox and McSweenwey1998; Singh, Reference Singh2004).
MUN concentrations the present study ranged from 12 to 18 mg/dl within the normal minimum and maximum limits for lactating Holstein cows (Meyer et al. Reference Meyer, Machado, Coldebella, Corassin, Cassoli, Coelho and Rodrigues2004). Higher MUN was observed for Holstein cows, but no effect of season and β-lg polymorphism was found. According to Arunvipas et al. (Reference Arunvipas, Dohoo, Van Leeuwen and Keefe2003), effects of non-nutritional factors on MUN, such as breed, stage of lactation and cow pregnancy, production and milk composition explain 13·3% of the variability of MUN concentrations.
Based on the results of this study, there was no association between milk composition (fat, lactose, total solids, TP, MTP, casein, casein:MTP ratio, somatic cell count and MUN) and β-lg genetic variant itself. During the dry season, independently of breed considered, higher contents of lactose, TP, MTP, casein and casein:MTP ratio were found.
The authors thank the Fundação de Amparo a Pesquisa do Estado de São Paulo for the financial support to conduct this study (Grant n° 02/12058-9), and José Franchini Garcia Moreno and Lucinéia Mestieri, for their technical assistance.
