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Transcript of Variation in blood leucocytes, somatic cell count, yield and composition of milk of crossbred goats
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Variation in blood leucocytes, somatic cell count,
yield and composition of milk of crossbred goats
Mainak Das, Mahendra Singh*
Dairy Cattle Physiology Division, National Dairy Research Institute, Karnal 132001, Haryana, India
Accepted 12 June 1999
Abstract
Ten multiparous crossbred goats, ®ve each of alpine � beetal (AB) and saanen � beetal (SB) were selected from the
National Dairy Research Institute goat herd immediately after parturition. These were managed as per the practices followed
in the institute's goatherd. Blood and milk samples were collected at biweekly intervals from day 14 post-kidding for 22 weeks
(154 days). Somatic cell count, electrical conductivity, fat, protein and lactose contents of milk were determined using
standard methods. In the blood samples total leucocytes and differential leucocytes were also determined. Somatic cell counts
were high immediately after parturition on day 14 of lactation and declined gradually with advanced lactation. There were
individual variations (P < 0.01) in somatic cell counts between different lactation periods. Somatic cell count of milk was
negatively correlated with neutrophils only (P < 0.05) and was neither correlated with milk yield, or with fat, protein, lactose
content of milk. Electrical conductivity of milk was low up to four weeks of lactation and thereafter increased as the lactation
advanced. Lactose content of milk declined gradually with the advancement of lactation. Fat content of milk was stable up to
the eighth week and thereafter increased with advancement of lactation while the protein content of milk did not change
signi®cantly during lactation. # 2000 Elsevier Science B.V. All rights reserved.
Keywords: Somatic cell counts; Blood cells; Electrical conductivity; Milk composition; Crossbred goats; Lactation
1. Introduction
The somatic cells that are sloughed off during the
normal course of milking have been characterized as
an index of udder in¯ammation like mastitis and for
the assessment of suitability of milk for marketing and
for manufacturing purpose (Smith and Roquinsky,
1977). The normal secretion in goats consists of
cytoplasmic particles, which break off and are shed
with the milk. Stage of lactation and season also affect
secretion of somatic cell counts in the milk (Dulin
et al., 1983; Lee et al., 1994; Wilson et al., 1995).
Information on the pattern of change of somatic cell
counts during entire lactation and also season in
crossbred goats under tropical condition is not avail-
able. The present study was therefore undertaken to
determine the levels of somatic cells in milk during
different stages of lactation and possible relations, if
any, with haematological parameters viz., total leuco-
cytes, lymphocyte, monocyte, neutrophil, eosinophil,
basophil and the yield and composition of milk.
Small Ruminant Research 35 (2000) 169±174
* Corresponding author. Fax: �91-0184-250042.
E-mail address: [email protected] (M. Singh).
0921-4488/00/$ ± see front matter # 2000 Elsevier Science B.V. All rights reserved.
PII: S 0 9 2 1 - 4 4 8 8 ( 9 9 ) 0 0 0 8 8 - 7
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2. Materials and methods
2.1. Experimental
Ten healthy crossbred goats, ®ve alpine � beetal
(AB) and ®ve saanen � beetal (SB) were selected
from the Institute's goatherd immediately after par-
turition. The experiment was started during the month
of November, 1996 and continued up to April, 1997
for a period of 22 weeks. All experimental goats were
in their second or third lactation. For the entire experi-
mental period goats were kept in a loose housing
system with brick ¯ooring. They received ad lib green
fodder, which consisted of berseem (Trifolium alex-
andrinum) and mustard (Brassica campestris). The
concentrate mixture having 70% total digestible nutri-
ents and 20% crude protein was fed based on milk
production (400 g per kg milk) at the time of milking.
The water was offered ad libitum to all the goats.
2.2. Blood and milk samples
The goats were hand-milked at 5:00 and 17:00
hours daily and the milk yields were recorded. Well
mixed milk samples were collected during morning
milking at biweekly intervals for 154 days. Aliquots of
milk samples from each goat in proportion to their
milk yields were taken and used for analysis of milk
constituents. Jugular blood samples were collected in
heparinized vacutainer tubes at 05:00 hours before the
start of milking. The maximum and minimum ambient
temperatures, relative humidity and vapor pressure
were also recorded during the period of study.
2.3. Statistical analysis
Statistical analysis of data was carried out using
two-way analysis of variance (ANOVA) as described
by Snedecor and Cochran (1980). Mean and standard
error of the different parameters and the correlations
among the parameters were calculated for each
biweekly period.
2.4. Analytical methods
In the fresh milk sample from each goat, milk fat
was determined by Gerber's method (ISI, 1958). The
lactose content of milk was estimated by picric acid
method (Perry and Doon, 1950) and the protein by
formaldehyde titration method (Singhal and Raj,
1989). Electrical conductivity (EC) of fresh milk
was measured using digital conductivity meter (cen-
tury make cc 601) standardized with goat milk.
Somatic cell counts (SCC) in fresh milk were counted
by the method of IDF (1984). l0 ml smear of milk was
made in an area of 20 � 5 mm on a glass slide and the
somatic cells were stained using methylene blue dye.
The somatic cells were counted in 50 ®elds and were
multiplied by the microscopic factor. In fresh blood
samples, total leucocyte count (TLC) and differential
leucocyte counts (DLC) namely, lymphocyte, mono-
cyte, neutrophil, eosinophil and basophil cells were
determined by the method of Jain (1986).
3. Results
Mean somatic cell counts, yield and composition of
milk and electrical conductivity for different experi-
mental periods has been shown in Table 1. The
average maximum and minimum ambient tempera-
tures varied from 16.738C to 29.378C and 4.468C to
15.358C during the experimental period. The average
values of THI (temperature humidity index) during
morning and evening were 49.35±76.67 and 48.95±
78.00, respectively. Mean SCC was higher during the
®rst biweekly period of lactation and declined steadily
with advanced lactation, but in individual goats con-
siderable variation (8.09±44.10 � 105 cells/ml) in
SCC existed. Goat AB-138 had very high SCC in
comparison to other goats from the beginning to the
end of the experiment. The goat when tested for
mastitis using California mastitis test was found to
have normal milk. On the other hand in another goat
SB-536, SCC was very low and varied between 5.50
and 8.09 � 105 cells/ml during lactation which indi-
cated that SCC varied between the animals. The
variations in SCC between the goats and between
different experimental periods were highly signi®cant
(P < 0.01). Further, the variation in SCC between the
two breeds of goats was also signi®cant (P < 0.05).
The SCC changes were almost stabilized from the
sixth biweekly period to the end of lactation. Cyto-
plasmic particles were more in early lactation as
compared to mid-lactation (data not presented). Elec-
trical conductivity of milk was low during ®rst two
170 M. Das, M. Singh / Small Ruminant Research 35 (2000) 169±174
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Table 1
Mean � standard error values of somatic cell counts, yield, percentage of fat, protein and lactose and electrical conductivity
Parameters Experimental period (biweekly)
1 2 3 4 5 6 7 8 9 10 11
Somatic cell count
(�105 cells/ml)
15.18 � 3.11 12.31 � 1.70 10.48 � 0.92 9.50 � 0.89 9.40 � 0.75 9.00 � 0.77 8.92 � 0.72 9.11 � 0.64 9.51 � 0.70 8.75 � 0.54 8.04 � 0.49
Milk yield (kg) 1.08 � 0.20 1.61 � 0.16 1.83 � 0.14 1.80 � 0.10 1.56 � 0.08 1.31 � 0.09 1.27 � 0.10 1.17 � 0.09 1.20 � 0.11 1.05 � 0.09 0.97 � 0.06
Fat (%) 3.48 � 0.06 3.58 � 0.07 3.43 � 0.09 3.46 � 0.08 3.61 � 0.06 3.58 � 0.05 3.71 � 0.04 3.84 � 0.06 3.96 � 0.05 4.27 � 0.05 4.32 � 0.05
Protein (%) 2.64 � 0.06 2.68 � 0.06 2.71 � 0.04 2.82 � 0.06 2.77 � 0.05 2.75 � 0.05 2.73 � 0.03 2.79 � 0.04 2.74 � 0.08 2.74 � 0.09 2.68 � 0.09
Lactose (%) 5.00 � 0.14 5.02 � 0.19 4.89 � 0.15 4.72 � 0.18 4.63 � 0.16 4.48 � 0.17 4.41 � 0.18 4.43 � 0.17 4.35 � 0.17 4.33 � 0.16 4.22 � 0.16
Electrical conductivity
(mhos)
2.10 � 0.03 2.01 � 0.01 2.15 � 0.04 2.36 � 0.05 2.48 � 0.06 2.86 � 0.05 3.13 � 0.06 3.72 � 0.11 4.10 � 0.13 3.69 � 0.08 3.53 � 0.06
Table 2
Mean � standard error value of hematological parameters for the experimental period
Parameters Experimental period (biweekly)
1 2 3 4 5 6 7 8 9 10 11
Total leucocyte
count (�103 cells/ml)14.71 � 0.59 14.95 � 0.60 14.55 � 0.58 14.29 � 0.57 14.04 � 0.55 13.98 � 0.59 14.13 � 0.57 14.38 � 0.55 14.63 � 0.61 13.80 � 0.56 13.51 � 0.63
Lymphocyte (%) 55.50 � 0.79 55.80 � 0.98 57.40 � 0.98 59.00 � 1.09 60.30 � 1.01 61.40 � 1.13 61.20 � 1.41 60.80 � 1.12 60.50 � 0.85 59.30 � 1.08 58.60 � 1.09
Monocyte (%) 5.30 � 0.43 4.80 � 0.54 3.10 � 0.54 0.90 � 0.48 0.10 � 0.09 0.10 � 0.09 0.30 � 0.20 1.60 � 0.53 1.20 � 0.56 1.80 � 0.64 2.50 � 0.53
Neutrophil (%) 33.60 � 0.65 34.40 � 0.01 35.40 � 0.75 37.10 � 0.71 37.80 � 1.15 37.80 � 1.14 37.60 � 1.62 36.50 � 1.54 36.60 � 1.31 37.20 � 1.42 35.90 � 1.40
Eosinophil (%) 4.80 � 0.46 4.10 � 0.79 3.10 � 0.87 2.30 � 1.00 1.80 � 0.64 0.70 � 0.28 0.70 � 0.25 0.80 � 0.28 1.20 � 0.42 1.10 � 0.39 1.70 � 0.32
Basophil (%) 0.80 � 0.19 0.90 � 0.26 0.80 � 0.31 0.70 � 0.45 ± ± 0.20 � 0.13 0.40 � 0.15 0.50 � 0.21 0.50 � 0.16 1.30 � 0.40
Table 3
Summary of ANOVA of complete data on SCC, milk yield and composition, EC and the hematological parameters
Source of variation d.f Mean sum of square
SCC Milk yield Fat Protein Lactose EC TLC Lymphocyte Monocyte Neutrophil Eosinophil Basophil
Between animals 4 12454b 0.315 0.281b 0.163b 1.31b 0.090 1940.8a 49.99b 10.42b 15.26 5.33a 1.468
Between groups 1 7767a 0.511 0.131a 1.035b 0.111 0.029 126.6 102.15b 18.41b 856.81b 191.14 0.582
Between
experimental period
10 4186b 0.917b 0.981b 0.286 0.790b 5.657b 249.2 43.00b 32.34b 19.61b 19.94b 1.485a
Error 94 1227 0.142 0.313 0.286 0.267 0.055 314.8 9.90 1.87 6.29 1.63 0.657
aP < 0.05.bP < 0.01.
M.
Da
s,M
.S
ing
h/S
ma
llR
um
inant
Resea
rch35
(2000)
169±174
171
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periods and increased thereafter till the ninth experi-
mental period of lactation (P < 0.01). The signi®cant
changes in EC (P < 0.01) during different periods of
experiment with no changes in EC of two breeds of
goats and between the goats indicated that EC of milk
changes with stages of lactation. Percentage of fat,
protein and lactose of milk varied (P < 0.01) between
the animals. The percentage of fat and lactose also
varied signi®cantly during different stages of lactation
(P < 0.01) but the protein content did not vary during
different periods of lactation. Somatic cell counts were
not correlated with any of the parameters viz., milk
yield, fat, protein, lactose and electrical conductivity
of milk. EC of milk was positively correlated with fat
content of milk (P < 0.01) and negatively with lactose
and milk yield. Fat content of milk was negatively
correlated with lactose (P < 0.01) and milk yield
(P < 0.05).
3.1. Hematology of the goats during lactation
The mean values of hematological parameters and
the summary of ANOVA of all parameters (Tables 2
and 3) showed that mean TLC was 14.95 � 103 cells/
ml during second period of lactation and declined
gradually to low values of 13.98 � 103 cells/ml in the
sixth period of lactation and thereafter ¯uctuated. The
changes in TLC during different experimental periods
in both breeds of goat were not signi®cant. Blood
lymphocytes also exhibited an increase in cell number
upto the 12th lactation and thereafter ¯uctuated being
50±70% in both the AB and SB breed. Due to greater
variability (P < 0.01) in lymphocytes of the two
breeds, the changes in blood lymphocytes between
different lactation periods and between the animals
were signi®cant (P < 0.01). The monocyte numbers
varied between 4 and 9% with mean values of 5.30%
during the ®rst two biweekly periods of lactation and
thereafter declined. During the ®fth and sixth periods
of lactation the monocyte counts were minimal and in
some of the goats was absent beginning fourth period
of experiment. Due to greater individual variation, the
changes in monocytes between the goats and between
different periods of lactation were signi®cant (P <
0.01). Further, breed difference in monocyte counts
was also signi®cant (P < 0.01). Average values of
blood neutrophils were low during the ®rst period,
increased gradually up to the seventh period and
thereafter remained ¯uctuating. On percent basis dur-
ing entire lactation of 154 days neutrophils were 30±
47%. The changes in neutrophil cell numbers between
animals were not signi®cant while differences in
experimental periods were signi®cant (P < 0.01).
The changes in neutrophil percent of the two breeds
of goats were also signi®cant (P < 0.01). Blood eosi-
nophils were high during the ®rst period and declined
as lactation advanced up to the sixth period of lacta-
tion. The pattern of change in eosinophil was similar
to the changes observed for blood monocytes. In some
of the goats, the eosinophils were almost absent in the
blood from the fourth period of lactation and there-
after, while in the remaining goats, their number
varied between 1% and 8% only. The variation in
eosinophils between the goats and during different
fortnights of lactation were highly signi®cant
(P < 0.01). However, both breeds of goats did not
exhibit signi®cant changes in eosinophil counts during
different lactation periods. Blood basophil cells did
not exhibit a distinct change during entire lactation.
The basophil were absent in blood of AB cross from
the ®fth period of lactation while in SB crosses, the
cells were absent from third to seventh period of
lactation. Since there was no distinct pattern of change
in basophils in different goats, the changes in the
basophil cells between animals and between breeds
were not signi®cant. However, variations in basophil
cells were signi®cant (P < 0.05) between lactation
periods.
4. Discussion
In the present study the SCC in different goats were
highly variable during different periods of lactation.
The high SCC in goat AB-138 was probably due to
inherent characteristics, as the goat udder remained
healthy throughout the period of study. The SCC
values observed in this study were similar to earlier
reports in goat (Park, 1991; Haenlein, 1987; Randy et
al., 1991; Hahn, 1992). The SCC are in¯uenced by
season, stage of lactation and productive stage of the
goats (Dulin et al., 1983; Randy et al., 1991; Wilson et
al., 1995; Muggli, 1995). Kasireddy (1983) reported
that SCC increase during second half of lactation and
were inversely related to milk yield. Hinckley (1984)
reported high SCC and high amounts of cytoplasmic
172 M. Das, M. Singh / Small Ruminant Research 35 (2000) 169±174
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particles in goat milk as observed in this study. Fat and
protein percents were signi®cantly correlated with
SCC in goat milk representative samples (Park and
Humphrey, 1986) but such correlations were not found
in the present study. Further, the kidding of goats
occurred in the month of November and lactation
continued up to April, but the effect of temperature
on SCC and other parameters studied was not clearly
discernible in this study. The trend in SCC during
different periods of lactation indicated that SCC
remains high during early lactation and with establish-
ment of lactation the SCC gets stabilized to basal
levels. The change in EC during lactation period was
in¯uenced by change in milk yield during lactation but
there was no correlation between SCC and EC of milk
as reported earlier by Park (1991). However, Lee et al.
(1994) reported a close relationship between SCC and
proportions of raw goat milk from individual goats
sampled once in a month. SCC from individual goat
milk was higher than those in goat bulk milk. EC of
milk depends on the concentration of cations and
anions in milk. Since sodium and chloride content
of milk increase during late lactation, the EC of milk
also increases with stage of lactation. The decline in
total leucocyte counts, basophils, eosinophils and
monocytes up to ®fth period of lactation indicated
their migration from blood into milk for more ef®cient
phagocytosis and mammary gland defense against
pathogens (Paape et al., 1992). Hinckley and Williams
(1981) reported poor correlation between SCC and the
leucocyte count. The role of neutrophils in lactation is
not clear but the increase in neutrophils may probably
be due to the increase in milk yield during early
lactation and thus contribute to high SCC in milk
(Drake et al., 1992). Since lymphocytes are of differ-
ent types, their role in lactation can only be predicted
when different types of lymphocytes are determined.
El-Nouty et al. (1984) reported that during mid-
lactation lymphocyte numbers increase while remain-
ing types of leucocyte decrease as observed in this
study also. The individual variations in cell numbers
and the absence of monocytes, basophils and eosino-
phils in the blood during certain periods of lactation
indicated that these cells probably do not have any
signi®cance with stage of lactation and the SCC of
milk, and therefore, it is very dif®cult to establish
reference values of these cells in goats (Masoni, 1985).
The decline in lactose percent concomitant to decrease
in milk yield and increase in fat content with advance-
ment of lactation was also reported earlier in goat
(Mukherjee et al., 1985; Zyugoyiannis and Katsaou-
nis, 1986; Kalla and Prakash, 1990; Simos et al.,
1991). However, Singh (1996) reported variation in
the fat, protein and lactose content of milk and
there was no effect of stage of lactation. From the
study it was concluded that SCC of milk in goats were
high during early lactation and decreased subse-
quently as the lactation advanced. Total leucocyte
count in blood also decreases as the lactation pro-
gresses and remains ¯uctuated during late lactation.
Lymphocytes and neutrophils were low during early
lactation and with establishment of lactation stabilize
to normal levels. Protein content of milk did not vary
during different periods of lactation. However, lactose
decrease and fat percent increase with advancement
of lactation.
Acknowledgements
The authors are thankful to the Director, National
Dairy Research Institute, Karnal for providing the
necessary research facilities to conduct the study.
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