Histopathology in Bovine Rotavirus (Type A) Infected Calves and Its Confirmation by
ELISA and RT-PCR
Rakib TM, Barua SR*, Siddiki AMAMZ, Masuduzzaman M, Hossain MA and Chowdhury S
Department of Pathology and Parasitology, Chittagong Veterinary and Animal Sciences University, Bangladesh
Submission: May 25, 2018; Published: July 10, 2018
*Corresponding author: Barua SR, Department of Pathology and Parasitology, Chittagong Veterinary and Animal Sciences University, Khulshi, Chittagong 4225, Bangladesh, Email: [email protected]
How to cite this article: Rakib T, Barua S, Siddiki A, Masuduzzaman M, Hossain M, Chowdhury S. Histopathology in Bovine Rotavirus (Type A) Infected
Calves and Its Confirmation by ELISA and RT-PCR. Dairy and Vet Sci J. 2018; 6(4): 555693. DOI: 10.19080/JDVS.2018.06.555693
The present study was designed to investigate the pathology of bovine rotavirus A infection in dead calves with the history of diarrhea. The cases were further confirmed by ELISA and RT-PCR. A total of 7 dead calves were examined by recommended post mortem techniques followed by confirmatory diagnostic tools. Four calves were found positive by both ELISA and RT-PCR assays. Grossly, no characteristic pathological lesions were observed except congestion in small intestine. The characteristic histopathological lesions were observed mainly in jejunum, ileum, Peyer’s patches and mesenteric lymphnode. Blunting of villi, lymphocytic infiltration, intracytoplasmic eosinophilic inclusion body, nuclear degradation and syncytia formation were observed under the microscope with different magnification. However, observation of pathological changes is important for identification rotaviral infection in case of doubtful specimens. To our knowledge, this is the first report from Bangladesh applying post-mortem examination, ELISA and RT-PCR for detection of bovine rotavirus group A from diarrheic dead calves.
Neonatal calf mortality is one of the most common animal health concerns for dairy industry which affect the herd health, farm profitability and as a whole the economy of the country. It has also been recognized as an important condition responsible for high morbidity and mortality in calf , particularly in the first month of age that was accounted about 84% of the total mortality [2,3].
Rotavirus represents as a significant cause of neonatal calf mortality which belongs to the family Reoviridae, genus Rotavirus and is non-enveloped, double stranded RNA virus, with a diameter of 65-70nm. Rotavirus infects primarily mature non-proliferating enterocytes lining the villi of small intestine. Rotavirus diarrhoea is caused by a combination of factors, which include reduction in epithelial surface area resulting in malabsorpation syndrome, activation of the enteric nervous system, and the effect of the rotavirus nonstructural protein . Mild catarrhal changes in the small intestine with congestion of both mucosa and serosal layers are also found [5,6]. The severity and localization of rotavirus intestinal infection vary among animal species and between studies ; however, the
pathological changes are almost exclusively limited to the small intestine. The small intestinal mucosa of neonatal calf consists of long finger-like villi, when challenged with different agents, the pathological changes are almost similar. The main pathological lesion consists of stunting and thickening of the villi. Frequently the villi are fused and leading to a flat mucosa in the severe cases. The epithelium covering such villi is generally cuboidal, and in rotavirus infection squamous epithelium covering the tip of some villi may be seen .
The presence of intracytoplasmic inclusion bodies in small intestinal enterocytes is the indication of viral etiology. The characteristic changes in rota viral infection are blunting of villi, thickening of crypts etc. The thinning of mesenteric lymph nodes is suggestive of lymphocytic migration as seen in the form of infiltration in mucosa. The histological changes in ileum are desquamation and necrosis of crypt with villous atrophy, infiltration of lymphocytes in inter villous areas and decreased population of lymphocytes in Peyer’s patches and mesenteric lymph node [1,2]. The presence of rotavirus antigen frequently found in the intestinal tissues and mainly confined to the small intestinal mucosa. Infected cells stained with H&E
staining method showed characteristic syncytia and eosinophilc
intracytoplasmic inclusion body.
It is noted that confirmatory detection of rotaviral infection
of diarrheic dead calves is very important but application of
different confirmatory diagnostic tests like ELISA and RT-PCR are
expensive. In this view, the objective of the study was selected to
identify of microscopic lesions of rotaviral infected dead calves
through postmortem examination and similarly confirmed by
ELISA and RT-PCR.
A total of 7 fecal samples/intestinal contents and tissue
samples were collected from dead cattle calves of up to 45 days
of age by postmortem examinations having history of clinical
diarrhea at the time of mortality from the selected areas during
the period July 2015 to June 2016. Fecal samples/intestinal
contents were collected from intestine using a disposable latex
glove. All standard precautionary measures were taken to
avoid contamination of samples and transported to the clinical
pathology laboratory on ice and stored at -20 until processing.
Intestinal tissue samples showing lesions suggestive of rotavirus
infection were collected and preserved in Bouin’s solution for
A 10% fecal suspension of individual sample was prepared in
phosphate buffered saline (pH 7.2) and clarified by centrifugation
at 13,000 rpm at 4°C for 10 minutes. The supernatant was
separated and allocated into two aliquots. After processing,
one aliquot was used to detect bovine rotavirus applying the
direct sandwich ELISA and rest aliquot stored at -70°Cuntil
RNA extraction for RT-PCR. Intestinal tissue samples were also
preserved in 10% buffered formalin until histopathological
The collected tissue samples were examined for
histopathological investigation following proper techniques. In
brief, the samples were preserved in Bouin’s solution for 2-3
days and subsequently, samples were made smaller size (5mm
thickness) and washed over night in running tape water. Then the
tissues were dehydrated by ascending ethanol series to prevent
shrinkage of cells as per following schedule. The tissues were
dehydrated in 50%, 70%, 70%, 80%, 90%, 95%, 100%, 100%,
100% alcohol, one hour in each; one hour in absolute alcohol and
absolute xyline mixture; two hours in 100% xyline, impregnation
was done in melted paraffin (60°C) for 3 changes and two
hours for each change. After this step, sample was kept at room
temperature overnight for drying. Then a block of sample was
made using melted paraffin. These blocks of tissue sample were
dried at room temperature. Then the blocks were sectioned with
a microtome at 5-μm thickness. A small amount of citric acid (or
gelatin) was added to the water bath (60°C) for better adhesion
of the section to the slide. The tissue sections were allowed to
spread on warm water both at 60°C. Then the sections were
taken on grease free clear slides. The slides containing section
were dried room temperature and kept in cool place. Finally, the
slide was prepared for routine hematoxylin and eosin staining.
The sectioned tissues were deparaffinized in two changes of
xyline (two minutes in each). Then the sectioned tissues were
rehydrated through descending grades of alcohol (100%, 100%,
95%, 80% and 70%; two minutes in each) followed by washing
in running rape water for five minutes. Then tissues were stained
with Harries hematoxylin for ten minutes and then washed
in running tap water for 15 minutes. Then the tissues were
differentiated in 1% acid alcohol (1part HCL and 99 parts 70%
alcohol) by 2-4 quick dips. Again, the slide washed in running
tap water for 5 minutes and followed by 2-4 dips in ammonium.
Again, the tissue sample was washed in running tap water for 10
minutes. After washing, the sections were stained with 1% eosin
for two minutes. Again, the tissue was dehydrated in ascending
grades of alcohol (70%, 80%, 95%, 100% and 100% alcohol; 30
sec, 45 sec, 2 min, 2 min and 2 min in each step; respectively).
Then the tissue sample was treated in absolute alcohol and
xyline mixture, 100% xyline for 2 minutes in each step. Finally,
the slide was kept in 100% xyline until mounting. Then stained
slide were mounted with cover slip using DPX mountant. Then
slides were dried at room temperature and examined under light
microscope at low (10x) and high (40x, 100x) power.
All the 7 fecal samples were used for viral RNA extraction.
Rotavirus RNA was extracted from the fecal suspension using
QIAamp Viral RNA mini kit (Qiagen/Westburg, Leusden,
Netherlands) following the manufacturer’s instructions. The
extracted RNA was stored at -80 °C.
The RT-PCR reaction was performed by using a QIAGEN
One Step RT-PCR Kit (QIAGEN) for the confirmation of bovine
rotavirus A. The primers used for amplifying a 294-bp fragment
of the VP6 gene of rotavirus A, the sequence of the upstream
primer was 5’-ACCACCAAATATGACACCAGC-3’; the sequence of
the downstream primer was 5’-CATGCTTCTAATGGAAGC-3’.
Before applying RT-PCR reaction, 7μl of viral dsRNA were
denatured at 95°C for 5 minutes and chilled immediately for
5 minutes. Then, reaction was carried out under the following
conditions: reverse transcription at 50 °C for 30 minutes, then
PCR with initial activation at 95 °C for 15 minutes followed by 40 cycles of amplification 94 °C for 30 seconds, annealing at 55
°C for 1 minute and extension at 72 °C for 1 minute, and a final
extension of 72 °C for 7 minutes. The amplified PCR products
were subjected to electrophoresis on 1.5% agarose gel stained
with ethidium bromide and observed under ultraviolet light.
Specific amplicon size for VP6 was observed on the stained gel.
All the seven samples were studied for histipathological
changes for bovine rotavirus infection. Out of 7 samples, 4
samples showed microscopic changes related rotaviral infection.
Blunting of villi and edema in lamina propria were found
microscopically (Figures 3-5). Severe infiltration of lymphocytes
was seen in mucosa occasionally extending up to the sub
mucosa (Figure 5). Eosinophilic intracytoplasmic inclusion
bodies were seen in the mucosal epithelial cells and a nuclear
fragmentation was observed in few epithelial cells (Figures
6-8). The changes were seen in the mucosa of the duodenum,
jejunum and ileum which revealed engorged capillaries and
infiltration of lymphocytes. Jejunum showed engorged blood
vessels in mucosa, sub mucosa and serosa with lymphocytic
infiltration in mucosal layer. Desquamated epithelial cells were
observed in the lumen. In ileum the changes were characterized
by desquamation and necrosis of crypts with villous atrophy.
Infiltration of lymphocytes could be seen in inter villous areas.
In Peyer’s patches, the lymphocytes were thinly populated,
clumped, and few areas showed nuclear fragmentation and
In the present study seven calves died with the history of
diarrhea revealed mild catarrhal changes in the small intestine
with congestion of both mucosa and serosal layers and these
changes were in agreement with earlier report. ELISA and RTPCR
screening of the fecal samples/ intestinal contents for the
presence of rotavirus antigen revealed positivity in 4 calves thus
confirming rotavirus infection. The presence of intracytoplasmic
inclusion bodies in small intestinal enterocytes was indicative
of viral etiology. The characteristic changes as blunting of villi,
thickening of crypts etc., was observed in the present study
were suggestive of rotaviral etiology. The thinning of mesenteric
lymph nodes was suggestive of lymphocytic migration as seen
in the form of infiltration in mucosa. Previous studies confirm
that rotaviruses are not able to produce severe gross changes in
intestinal mucosa by their own . The histological changes in
ileum characterized by desquamation and necrosis of crypts with
villous atrophy, infiltration of lymphocytes in inter villous areas
and decreased population of lymphocytes in Peyer’s patches and
mesenteric lymph node were in agreesment with earlier reports
Rotavirus infection is implicated mainly in neonatal calves.
The gross lesions of rotavirus infection are the nonspecific
findings of undifferentiated neonatal diarrhea in calves.
However, histopathology could be indicative; blunt, club-shaped
villi, mild or moderate villus atrophy and perhaps villus fusion
may be present [12,13]. Villi covered by low columnar, cuboidal,
or flattened surface epithelium with a poorly defined brush
border. There is usually a moderate proprial infiltrate of mononuclear
cells and eosinophilic or neutrophils and hypertrophic
crypts may be evident. Lesion and viral antigen always should be
sought in the distal small intestine and preferably several sites
along its length [13,14
Rotaviruses replicate in the non-dividing mature enterocytes
near the tips of the villi, suggesting that differentiated
enterocytes express factors required for efficient infection
and replication . The severity and localization of rotavirus
intestinal infection vary among animal species and between
studies; however, the pathological changes are almost exclusively
limited to the small intestine. In various animal models, rotavirus
infection was associated with virtually no visible microscopic
lesions; slight lesions, such as enterocyte vacuolization and loss;
or larger changes, such as villus blunting and crypt hyperplasia.
Inflammation is generally mild compared to that for other
intestinal pathogens. This picture of pathology suggests that
there is no absolute correlation between histological lesions and
disease symptoms. Rotavirus infection alters the function of the
small intestinal epithelium, resulting in diarrhea. The diarrhea
was generally considered to be malabsorptive, secondary to
enterocyte destruction .
The mucosa of small intestine of the neonatal calf consists
of long finger-like villi and pathological changes due to different infectious
agents are almost similar . The most significant pathological lesion
consists of stunting and thickening of the villi and the villi are fused
leading to a flat mucosa in the most severe cases. The epithelium covering
such villi is generally cuboidal and in rotavirus infections squamous
epithelium covering the tip of some villi may be seen [12,16]. Erosion of
small areas of epithelium has been observed in rotavirus infections.
Rotavirus, by itself, causes slight to moderate shortening
(atrophy) of villi in the jejunum and ileum. The villi are blunt
and covered by immature epithelial cells. When the rotavirus
is accompanied by a pathogenic strain of Escherichia coli, the
lesions are similar but more severe. There is degeneration
and sloughing of cells from the villous tips, and bacteria are
adherent to cell surface. Stunting and fusion of villi, exfoliation,
disarrangement and vacuolation of enterocytes and the presence
of cuboidal enterocytes were observed in infected calves but not
in rotavirus-free control calves [17,18]. Lesions predominated in
the upper small intestine, where rotavirus was most abundant,
especially on the first two days of virus excretion. The numbers
of enterocytes infected with rotavirus diminished before the
In our study, histopathological changes agreed with the
positivity of ELISA and RT-PCR test results. Microscopic lesions
like, edema, infiltration of lymphocytes, nuclear fragmentation,
syncytia formation, eosinophilic intracytoplasmic inclusion body
observed only in those specimens that were the rotavirus cases
confirmed by ELISA and RT-PCR.
Rotavirus infection in the present study revealed rotavirus
specific lesions, such as denudation at tips of the villi, villus
blunting and necrosis of crypts along with intracytoplamic
inclusion bodies. The presence of rotavirus antigen in clinical
samples/affected tissues was also confirmed by ELISA and RTPCR.