dc.contributor.author |
De Silva, K.I.M. |
|
dc.contributor.author |
Rathnakumara, W.M.T.D. |
|
dc.contributor.author |
Abayalath, N. |
|
dc.contributor.author |
Alexander, P.A.B.D. |
|
dc.contributor.author |
Wijayagunawardhane, M.P.B. |
|
dc.contributor.author |
Kodithuwakku, S.P. |
|
dc.date.accessioned |
2023-01-16T10:24:17Z |
|
dc.date.available |
2023-01-16T10:24:17Z |
|
dc.date.issued |
2017-11-24 |
|
dc.identifier.citation |
De Silva, K. I. M., Rathnakumara, W.M.T.D., Abayalath, N., Alexander, P.A.B.D., Wijayagunawardhane, M.P.B. and Kodithuwakku, S.P., (2017), “Early Pregnancy Diagnosis Using Transrectal Colour Doppler Ultrasonography and Serum ISG15 mRNA assay in Dairy Cows” Peradeniya University International Research Sessions, University of Peradeniya, Sri Lanka |
en_US |
dc.identifier.uri |
http://ir.lib.ruh.ac.lk/xmlui/handle/iruor/10189 |
|
dc.description.abstract |
Introduction: Early pregnancy diagnosis is
an important factor in the management of
reproduction in dairy cows. However, tools
for accurate detection of non-pregnancy or
pregnancy status within first 21 days of
insemination are limited. Colour Doppler
ultrasonography, which allows detailed
assessment of the uterus, ovarian follicles
and corpora lutea, has been utilized as a
successful technique for bovine pregnancy
detection. Interferons are involved in
maternal recognition of pregnancy and
interferon-stimulated genes (ISG) are up regulated during pregnancy. The present
study examined the suitability of two novel
techniques based on these concepts to
diagnose pregnancy in early gestation.
Materials and Methods: Transrectal
ultrasound examinations were performed in
16 synchronized and artificially inseminated
(AI) cows at day 20 post-AI (pAI). Images
of corpus luteum blood flow (CLBF) were
obtained using colour ultrasound scanner
(CDUSS) and the images were analysed
using image analysis software ImageJ.
Animals were categorized as pregnant or
non-pregnant based on the results of CLBF
and confirmed on day 45 pAI by per-rectal
palpation. Serum was collected from the
same set of animals on day 20 pAI and
polymerase chain reactions (PCR) were
performed to identify ISG15 mRNA using
extracted RNA. Differential expressions of
ISG15 in pregnant and non-pregnant cows
were analysed using semi-quantitative RT PCR.
Results: Significantly higher (p<0.05)
arterial CLBF was observed in pregnant
cows at day 20 pAI. The CLBF had only
60% accuracy in detecting non-pregnancy.
A sensitivity of 100% was achieved in
detection of pregnant animals and 60%
specificity for determination of non pregnant animals through CLBF analysis. A
100% negative predictive value (NPV)
reflected the absence of false negative
results. The overall accuracy of CLBF
evaluation on day 20 was 75%. Semi quantitative PCR analysis revealed a
significant up-regulation in the ISG15 gene
in pregnant compared to non-pregnant cows
(p<0.05) on day20 pAI.
Discussion: The main purpose of early
pregnancy diagnosis is to re-breed the non pregnant animals as early as possible to
produce one calf per year. The findings of
this study support non-pregnant
identification (NPV=100%) at day 20 pAI
using CDUSS. Primary factors resulting in
false positive diagnosis could be early
embryonic losses between days 20 and 45
pAI, extended oestrous cycles with delayed
CL regression and short oestrous cycles with
ovulation in the same ovary, rather than
misdiagnosis. ISG15 mRNA is reported to
be up-regulated after day 16, peak at day 20
and decline by day 32. This experiment
should be extended with real-time
quantitative PCR to confirm the change in
gene expression.
Introduction: Early pregnancy diagnosis is
an important factor in the management of
reproduction in dairy cows. However, tools
for accurate detection of non-pregnancy or
pregnancy status within first 21 days of
insemination are limited. Colour Doppler
ultrasonography, which allows detailed
assessment of the uterus, ovarian follicles
and corpora lutea, has been utilized as a
successful technique for bovine pregnancy
detection. Interferons are involved in
maternal recognition of pregnancy and
interferon-stimulated genes (ISG) are up regulated during pregnancy. The present
study examined the suitability of two novel
techniques based on these concepts to
diagnose pregnancy in early gestation.
Materials and Methods: Transrectal
ultrasound examinations were performed in
16 synchronized and artificially inseminated
(AI) cows at day 20 post-AI (pAI). Images
of corpus luteum blood flow (CLBF) were
obtained using colour ultrasound scanner
(CDUSS) and the images were analysed
using image analysis software ImageJ.
Animals were categorized as pregnant or
non-pregnant based on the results of CLBF
and confirmed on day 45 pAI by per-rectal
palpation. Serum was collected from the
same set of animals on day 20 pAI and
polymerase chain reactions (PCR) were
performed to identify ISG15 mRNA using
extracted RNA. Differential expressions of
ISG15 in pregnant and non-pregnant cows
were analysed using semi-quantitative RT PCR.
Results: Significantly higher (p<0.05)
arterial CLBF was observed in pregnant
cows at day 20 pAI. The CLBF had only
60% accuracy in detecting non-pregnancy.
A sensitivity of 100% was achieved in
detection of pregnant animals and 60%
specificity for determination of non pregnant animals through CLBF analysis. A
100% negative predictive value (NPV)
reflected the absence of false negative
results. The overall accuracy of CLBF
evaluation on day 20 was 75%. Semi quantitative PCR analysis revealed a
significant up-regulation in the ISG15 gene
in pregnant compared to non-pregnant cows
(p<0.05) on day20 pAI.
Discussion: The main purpose of early
pregnancy diagnosis is to re-breed the non pregnant animals as early as possible to
produce one calf per year. The findings of
this study support non-pregnant
identification (NPV=100%) at day 20 pAI
using CDUSS. Primary factors resulting in
false positive diagnosis could be early
embryonic losses between days 20 and 45
pAI, extended oestrous cycles with delayed
CL regression and short oestrous cycles with
ovulation in the same ovary, rather than
misdiagnosis. ISG15 mRNA is reported to
be up-regulated after day 16, peak at day 20
and decline by day 32. This experiment
should be extended with real-time
quantitative PCR to confirm the change in
gene expression. |
en_US |
dc.language.iso |
en |
en_US |
dc.publisher |
Peradeniya University International Research Sessions, University of Peradeniya, Sri Lanka |
en_US |
dc.title |
Early Pregnancy Diagnosis Using Transrectal Colour Doppler Ultrasonography and Serum ISG15 mRNA assay in Dairy Cows |
en_US |
dc.type |
Article |
en_US |