Abstract:
The serological prevalence of Coxiella burnetii in domestic livestock in
Saudi Arabia was studied using two serological tests: indirect enzyme
linked Immunosorbent assay (ELISA) as the main test and indirect
immunofluorescence assay (IFA) as a confirmatory test and for
.comparison with ELISA
A total of 1970 farm animals of both sexes were tested serologically to
determine the prevalence of C. burnetii specific IgG antibodies using
indirect ELISA. The samples were collected from 489 camel, 428 cattle,
630 sheep and 423 goats. The animals were broadly divided into young
and adult animals. All of them were clinically normal when sampled and
.none of the adult females was pregnant while some were lactating
A total of 605 animals had anti-C. burnetii IgG antibodies in their sera,
giving an overall serological prevalence of Q fever of 30.71% with a
mean ELISA titre (S/P ratio or O.D.%) of 103.03%. These results indicate
that C. burnetii is common in all species a of farm animals in Saudi
Arabia. Camels showed the highest proportion of Q fever (C. burnetii)
positive sera among all the species tested, with an overall prevalence of
51.53%. The second highest serological prevalence was recorded in goats
(34.04%), followed by cattle (30.61%) and the least in sheep (12.38%). In
all species, the serological prevalence of anti-C. burnetii antibodies was
significantly higher in adult compared to young animals (p<0.0001).
Females animals tended to be more commonly affected than males;
however, statistical analysis revealed non-significant inter-sex difference
(p= 0.5847). Antibodies against C. burnetii in domestic livestock were
also investigated using ELISA assay in 285 defatted milk samples
obtained from 48 she-camels, 90 cows, 60 ewes and 87 does. Milk
samples from 30 camels (62.5%), 30 cows (33.3%), 24 goats (27.6%) and
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3 ewes (5%) were positive for anti-C. burnetii antibodies. Serum samples
from the same animals were simultaneously tested by ELISA. Of these,
32 camels (66.66%), 38 cows (42.2), 13 goats (14.9%) and 4 ewes
(6.67%) were positive for anti-C. burnetii antibodies. Statistical analysis
show a significant correlation between ELISA results in milk and serum.
Serum samples from a total of 307 animals, comprising 92 camels, 72
cows, 72 sheep and 71 goats, were also subjected simultaneously to
indirect immuno-fluorescence (IFA) and ELISA assays. A statistically
significant correlation was found between the serological prevalence of Q
fever as determined by these two assays. Using ELISA as a reference
serological test, statistical analysis showed that both the sensitivity and
specificity of IFA assays were good, indicating that either ELISA or IFA
can be used for screening Q fever in farm animals or as confirmatory tests
to one another. The shedding of C. burnetii by serologically positive
animals was investigated by the polymerase chain reaction (PCR), using
primers that amplify the repetitive transposon-like region of C. burnetii.
The study was conducted on 82 whole blood, 72 milk, 29 faecal and 21
urine samples collected from camels. In addition, 29 milk samples and 7
whole blood samples from cattle, 38 whole blood, 29 milk and 20 faecal
samples from goats and 22 blood samples from sheep were available for
.PCR analysis
Out of a total of 149 whole blood samples collected from these different
animal species, 13 samples (15.85%) from camels and 2 samples (5.6%)
from goats showed positive amplification for C. burnetii DNA while all
22 sheep and 7 bovine blood samples were negative. Out of 144 milk
samples collected from camels, cattle and goats, 5 samples (6.49%) from
camels, 11 samples (28.94%) from cows and 0 samples from goats were
positive for C. burnetii DNA. In addition, faecal samples collected from
29 camels and 20 goats revealed positive PCR products from 8 (27.59%)
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and 12 (60%) samples, respectively. C. burnetii DNA was also
demonstrated in 5 (23.81%) out of the 21 urine samples collected from
camels. All sampled subjected to PCR analysis were from serologically
positive animals with the exception of urine samples which were
collected from slaughtered camels that were not serologically tested for
anti-C. burnetii antibodies. Serum samples from known Q fever-positive
and known Q-fever negative animals were used to study the possible
effects of Q fever on various biochemical and electrolyte parameters. A
total of 281 serum samples were collected from camels, sheep, goats and
cattle. In all species, no significant differences were found between
Q-fever positive and Q-fever negative animals. However, a few
intra-specific differences existed within each species. The effect of Q
fever was also investigated in the levels of anti-oxidant enzymes, namely
thiobarbituric acid reactive substances (TBARS) and reduced glutathione
(GLUTH). TBARS level was determined in 239 known Q fever-positive
and Q fever-negative animals while GLUTH level was determined in 188
known Q fever-positive and Q fever-negative animals. No significant
differences in TBARS levels were found between Q fever-positive and Q
fever negative animals in samples collected from each of goats, camels
and sheep. However, the GLUTH level was found to be significantly
reduced (p<0.002) in Q fever-positive camels as compared to Q fever
negative camels. This enzyme is found in the cytoplasm of almost all
mammalian cells, and a reduction in its activity could indicate some
degree of cellular damage. However, further studies are needed to verify
.this aspect
This study constitutes the first record of C. burnetii in cattle, sheep and
goats in Saudi Arabia and the second, and more detailed, study on camels
.in the country