Immunohistochemical and histopathological studies of fixed rabies virus
in goats
S. ATALAY VURAL1* , G. ALCIGIR1 and S.
BERKIN1
ABSTRACT The purpose
of this study was to systematically demostrate and compare the development of
pathological and immunohistochemical changes in goats which were infected by a
fixed rabies virus that was used in vaccines’ production. The results are as
follows:
In histopathological examinations, varying degrees of inflammatory, degenerative, and necrotic
changes were detected in the central nervous system; in the immunoperoxidase
(IP) method, intra-and/or extracellular viral antigens were observed on the
cerebellum, cornu ammonis, thalamus, pons cerebri, nucleus caudatus, spinal
cord, medulla oblongata, Gasserian ganglion, eye and the retropharyngeal lymph
nodes; in the immunofluorescence (IF) method, intra-and/or extracellular viral
antigens were also seen in the same locations with the exception of
retropharyngeal lymph nodes. It was also observed that the antigens were qualitatively
and quantitatively well stained with both of methods. However the visibility of
antigens in the retropharyngeal lymph nodes besides the central nervous system,
and eye and the facilities of applying made the IP method much more
advantageous than the IF method.
Keywords : Rabies
virus, histopathology, immunoperoxidase, immunofluorescence
INTRODUCTION
Rabies viruses include the street
virus, the causative agent of rabies in humans and animals through natural
transmission, and the fixed rabies virus, a laboratory adapted form. The latter
virus was developed by Pasteur with serial intracerebral passages of the street
virus (Sullivan1993). The virulence and incubation period of the fixed rabies
virus are constant (Buxton & Fraser 1977; Jayakumar, Ramadass &
Baghavan 1989). It is employed in many ways, such as in studying the
replication of viruses and in the development of vaccines (Tordo &
Kouknetzoff 1986; Consales, Valentini, Albas, Mendonca, Fuches, Soares &
Pereira 1988).
For the diagnosis of naturally occuring rabies by
histopathological examination, it is important to demonstrate the presence
of Negri bodies in addition to the
nonpurulent encephalomyelitis.
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1 University
of Ankara, Faculty of Veterinary Medicine, Department of Pathology, 06110 Ankara, Turkey. e-mail :
svural@veterinary.ankara.edu.tr
However,
Negri bodies are found in only 50-80 % of the cases (Goldwasser &
Kissling 1958; Atanasiu, Dragonas, Tsiang & Harbi 1971;
Koprowski 1973). Demonstration of the viral antigen by the use of
immunohistochemical methods greatly increases the chances of diagnosing the disease. There is an 87-98 % possibility
of diagnosing rabies by using the immunoperoxidase (IP) method, and 87-100 % by
the immunofluorescent (IF) method (Anjaria & Jhala 1985;
Kotwal &
Narayan 1985, 1987; Jayakumar et al.
1989; Zimmer, Weigand, Manz, Frost, Reinacher & Frese 1990).
Since Negri bodies are not formed following inoculation of animals with fixed
rabies virus, it is impossible to detect infection on histopathological
examination as in the case of street virus infection. However, IP and IF
methods are employed to detect viral antigens in the tissues and organs of
animals experimentally inoculated with the fixed rabies virus (Madhusudana &
Tripathi 1990; Jackson & Park 1998).
The purpose of this study was to systematically demostrate
the development of pathological and immunohistochemical changes in goats which
were infected by a fixed rabies virus that was used in vaccines’ production.
The results were compared with each other.
MATERIALS AND METHODS
The examined materials were obtained
from ten goats, each of which was infected by the intracerebral inoculation of
0.2 ml of diluted Challenge Virus Standard (CVS) used for the production of a
rabies vaccine by the Etlik Veterinary Control and Animal Diseases Research
Institute, in Turkey. These animals were slaughtered when became agonized after
the injection.
Tissue
samples after conducting a post mortem examination of each animal were taken
from the cornu ammonis, nucleus caudatus, thalamus, pons cerebri, cerebellum,
medulla oblongata, cervical spinal cord, Gasserian ganglion, parotid and submandibular
salivary gland, retropharyngeal lymph node, vestibular region of the nose, an
intact eye, skin around the ear and mouth, trachea, thymus, lung, heart,
spleen, liver, kidney and adrenal gland. These samples were fixed in 10 %
buffered formalin, and embedded in paraffin wax. Sections were stained with
hematoxyline and eosin, and if deemed necessary,
Periodic acid-Schiff, luxol fast
blue, for histopathological examination (Luna 1968). Fixed rabies virus
antigens in the tissues were demonstrated by using polyclonal rabbit
antinucleocapsid protein sera (obtained from the Rabies Centre of Expertise OIE
Reference Laboratory for Rabies WHO Collaborating Centre Animal Disease
Research Institute, Canada) by means of a modified IP method (Strept-Avidin
Biotin Peroxidase) and an indirect IF method (Heyderman 1979; Noorden &
Polak 1983; Fekadu, Greer, Chandler & Sanderlin 1988;
Vural 1997).
RESULTS
In the macroscopical examinations,
the meningeal blood vessels were seen congested. In two cases, the retropharyngeal
lymph nodes were swollen, and cut surface appeared to be more moist than usual
and dark brownish in colour.
In the histopathological
examinations, many of the blood vessels in the central nervous system were
hyperaemic and surrounded by lymphocytic cells in which there were small
amounts of macrophages (Fig. 1a).
Similar perivasculer infiltrations were
also observed in the meningeal blood vessels of the cerebral cortex,
cerebellum, pons cerebri, thalamus, and nucleus caudatus. Some neurons were
found to be degenerative, or necrotic (Fig. 1b-d). The Nissl bodies in the
neurons of the pons cerebri, cerebellum, medulla oblangata, and spinal cord
were distributed in an irregular rough granular form or located at the periphery of the cytoplasm in the form
of small granules. Some neurons of the medulla oblongata, pons cerebri, and
spinal cord of the animals were atrophic. Neuronophagia was apparent in the
cornu ammonis, cerebellum (Fig. 1a), thalamus (Fig. 1c), pons cerebri, medulla
oblongata, spinal cord, and Gasserian ganglion. Babes’ nodules were also
observed in the cerebellum, thalamus, and pons cerebri. Focally or diffusely
distributed proliferation of glia cells was noticed in the cornu ammonis,
cerebellum, thalamus, pons cerebri, medulla oblongata, and spinal cord. Focal
areas of demyelination in the cerebellum was observed in some animals. Focal
haemorrhages was noticed in the Gasserian ganglion (Fig. 1d), spinal cord, and
cornu ammonis. Perivascular oedema was also present in the pons cerebri of some animals. The extent
of the varying degrees of nonpurulent encephalitis or meningoencephalitis
observed in the animals is summarized in Table 1.
In the kidneys, some glomerular
capillaries appeared to have taken the form as wire loops and others had
undergone atrophy. The parietal membrane of Bowman capsules and the tubular
basal membranes were thickened. Fibrosis was observed in some intertubular
areas of the medullary regions and the
areas surrounding the glomeruli where atrophy was present.
Sinus catarrh was seen in the most
of retropharyngeal lymph nodes. The lymphoid follicules were hyperplastic and
lymphoblasts were present in the central regions. Thymus was also hyperplastic.
Lymphocytic cells and sparsely distributed macrophages were noticed in the
vestibular region of the nose and trachea particularly around some glands.
In the preparations stained by the
IP method, viral antigens were observed (Table 1) in the Purkinje cells,
cerebellar peduncle neurons, and the stratum granulosum nerve cells of the
cerebellum (Fig. 2a), pyramidal and
cerebral cortex neurons of cornu ammonis, thalamus (Fig. 2b), pons cerebri
(Fig. 2c), nucleus caudatus, spinal cord, medulla oblongata (Fig. 2d),
Gasserian ganglion, eye and retropharyngeal lymph nodes. They were seen as a
fine dust or rough granules from brick-red to brown in colour in the perikaryon
and extensions (axon and dendrites) of the neurons, glia cells and freely
around them in the nervous system. They were also seen in the perivascular
lymphocytic cells, endothelial cells and some ependimal cells of the pons
cerebri, and the medulla oblongata.
In IF stained preparations, the
viral antigens were observed (Table 1) in the same regions of central nervous
system (Fig. 3a-d), Gasserian ganglion, and eye. The presence of viral antigens
was revealed by the presence of glistening, yellow, mostly fine granules and
some coarser particles. The granules in some sections were so big that they
could be mistaken for inclusion bodies.
DISCUSSION
The necropsies of animals infected
with fixed rabies viruses are generally reported not to reveal any pathological
changes (Burkhart, Jervis & Koprowski 1950) or as seen in this
study, only hyperemia in brain vessels was reported (Sinchaisri, Nagata,
Yoshikawa, Kai &
Yamanauchi 1992).
Perivascular mononuclear cell
infiltration, glia cell proliferation, neuronal degeneration, neuronophagia and
demyelination noticed in this study have also been reported as a
histopathological changes found most frequently in the cerebral and cerebellar
cortices, pons cerebri, spinal cord, and Gasserian ganglion (Burkhart et al. 1950; Field 1951; Johnson 1965;
Jackson &
Park 1998). Inflammatory reactions reported in the meninges (Burkhart et al. 1950; Field 1951; Johnson 1965;
Jackson &
Park 1998), were also observed around the blood vessels on the meninges
covering the cerebral cortex, cerebellum, thalamus, pons cerebri and nucleus
caudatus in this study. In addition to these, perivascular oedema was seen in
the meninges of the pons cerebri. Field (1951), has described the rough
appearance of the Nissl granules in the neurons, and has stated that this is
often encountered in the pons cerebri. Similar observations were seen in the
neurons of the pons cerebri, medulla oblongata, spinal cord and cerebellum in
this study. Neuronal degeneration and necrosis result from infection with fixed
rabies virus, as in other studies (Miyamoto & Matsumoto 1966;
Sullivan1993) except for the primary forms of the inclusions observed under
electron microscopes, no inclusion bodies are encountered.
The wire loops formation
of the glomerular blood vessels and the thickening of the parietal membrane of Bowman capsules and
the tubular basal membranes in the kidneys of the vaccinated animals were
thought to be the result of antigen-antibody complexes.
Fixed rabies viral antigens in IP preparations mostly
concentrate in the cerebrum, cerebellum, pons cerebri, brain stem and the
dorsal root ganglion of this region, spinal, and trigeminal nerves (Jackson,
Reimer &
Ludwin 1989; Jackson & Wunner 1991; Sinchaisri et al.1992; Jackson &
Park 1998). In this study, IP positivity was encountered in the cornu ammonis,
cerebellum, thalamus, pons cerebri, spinal cord, medulla oblongata, nucleus
caudatus, Gasserian ganglion, eye, and retropharyngeal lymph nodes. On the
other hand, the antigens were mostly found in substantia grizea besides in
substantia alba, is similar to the findings in this study in which either that
relatively higher chances of finding antigens in this region or that antigens
are never found there (Jackson et al. 1989; Jackson & Wunner
1991).
The viral antigens in IF
preparations have mostly shown on the cerebrum, cerebellum, brain stem, and
the dorsal root ganglion of this region, spinal cord, trigeminal nerves, eye,
heart, nasal mucosa, trachea, lung, kidneys, urinary bladder, adrenal gland,
oral, stomach, the Averbach and Meissner plexus of the intestines, hair
follicle, and muscle (Correa-Giron, Allen & Sulkin 1970; Ravaioli, Palliola, Pestalozza,
Granieri & Ciucnini
1970; Fischman &
Schaeffer 1971; Johnson & Mercer 1964; Kucera, Doliva, Coulon &
Flamand 1985; Coulon, Derbin, Kucera,
Lafay, Prehaud & Flamand 1989; Tsiang, Lycke, Ceccaldi,
Ermine & Hirardot 1989;
Mathusudana & Tripathi
1990; Tsiang, Ceccaldi & Lycke 1991). In this study, the
positiveness of IF is almost in similar
in central nervous system. Although retropharyngeal lymph nodes have not
examined in the literatures, it was examined. But no antigens were seen.
Johnson &
Mercer (1964) reported that viral antigens become localised only in the
neurons, but not in glia, meningeal, ependymal, or vascular cells and they tend
to be concentrated in the neurons close to the ependymal cells and in the axons
on the substantia alba, that IF positivity tends to increase especially in the
perikaryons and extensions of the Purkinje cells, and that viral antigens show
irregular distribution on the cornu ammonis, cerebrum, brain stem, cerebellum
and the anterior regions of the spinal cord. In this study, viral antigens were
encountered not only in neurons, but they also in extraneuronal regions close
to the neurons and in some glia cells.
Despite the same tissues were examined as being mentioned in
several articles (Fischman & Schaeffer 1971; Madhusudana &
Tripathi 1990; Jackson & Wunner 1991), in this study fixed rabies
viral antigens were not observed in the IF and IP preparations except central nervous system, eye, and
retropharyngeal lymph nodes. In addition, contrary to the literature, viral
antigens could not be traced in the IF and IP preparations in two of the cases
necropsied despite the inflammation changes observed in all the animals. This
insignificant variations obtained in
this study is considered to be the result of the result of the viral antigen
being denatured during a time period, differences in inoculation methods, and
concentrations and strains of the viruses used. During the study it was found
that organs from different animals yielded different results for the two
methods. This has been ascribed to practical errors has. This was noticed in
the qualitative and quantitative evaluation in the tissues and cells of the
viral antigens.
Tsiang, Koulakoff, Bizzini & Berwald-Netter
(1983) in IF examinations of neuroblastoma and dorsal root ganglion cell
cultures infected with CVS reported the finding one to two cytoplasmic
inclusions in each cell. However, Sinchaisri et al. (1992) could not detect inclusion bodies formed by viral
nucleoprotein in cytoplasm and they attributed that these results to the fact
that either the animals died before the viral antigens could accumulate in
sufficient quantity to form inclusion bodies or they related it to the
experimental conditions that they used. Although inclusion bodies were not
seen, it could not be determined whether or not the large granules observed in
the IP and IF preparations were inclusion bodies in this study.
In the histopathological examinations of this study, the
extent of the varying degrees of nonpurulent encephalitis or
meningoencephalitis were observed. But, they were usually seen in central
nervous system caused by many viral diseases. For doing a differentiative
diagnosis, the immunohistochemical examinations had to be done. Thus, it was
shown that the fixed rabies virus antigen in formalin-fixed and
paraffin-embedded tissue sections were seen clearly by using the IP and IF
methods in this study. But, the IF method requires fluorescent microscopy and
fresh preparation of procedure each time. On the other hand, the IP method
could be able to use with ordinary light microscope and it has practical
importance for the laboratories. All the slide preparations in IP method were
permanent which means they were available for storing and rechecking. As a
result, the antigens were also well-stained by these methods in both tissue
sections but they were more qualitatively and quantitatively in IF method than
IP method. But, the IP method proved to be much more advantageous for a viral
antigens to be in different tissue as being retropharyngeal lymph nodes and the
positiveness of results obtained from eye was much more than the IF method.
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Acknowledge: I thank Alexander Wandaler
for hyperimmun sera and Ismet Yoruk for obtained materials. This work was
supported University of Ankara, Research Fund.
FIG. 1a Hyperaemia, perivascular infiltration (thin arrow) and neuronophagia
(thick arrow) in the cerebellum HE X100
FIG. 1b Neuronal necrosis (arrow) in the pons cerebri HE X320
FIG. 1c Neuronal necrosis (arrow) and neuronophagia (thick arrow) in the
thalamus HE, X200.
FIG. 1d Neuronal necrosis (thin arrows) and haemorrhagia (thick arrow) in the
Gasserian ganglion HE X400
FIG. 2a Granular and/or diffuse IP
positive staining in Purkinje cells (thin arrows) and extensions (thick arrows)
X250
FIG. 2b IP positive staining in a neuron and extensions (thin arrows) and
neuropil (thick arrow) of thalamus X250
FIG. 2c IP positive staining in neurone and extensions (thin arrows) and
neuropil (thick arrows) of the pons cerebri X250
FIG. 2d IP positive staining in the medulla oblongata (thin arrows) X320
FIG. 3a IF positive staining in neurone and extensions (thin arrows) and
neuropil (thick arrow) of cornu ammonis X320
FIG. 3b IF positive staining in a neuron (thick arrows) and extensions (thin
arrows) of the pons cerebri X320
FIG. 3c IF positive staining in the thalamus (thin arrows) X320
FIG. 3d IF positive staining in the nucleus caudatus (thick arrows) X320
Dr. Sevil Atalay Vural
University of Ankara, Faculty of Veterinary Medicine
Department of Pathology,
06110 Dıskapı, Ankara/TURKEY
e-mail: svural@veterinary.ankara.edu.tr
Fax: +(90) 312. 317 83 81 / +(90) 312. 316 44 72
November 24, 2000
Prof J. BOOMKER
ARC-Onderstepoort Veterinary Institute
Private Bag X05, Onderstepoort 0110, South Africa
Dear
Prof Boomker,
Thank you very much for
referees’s advice and help dated September 12, 2000. I met the requirements of
the referee and sent manuscripts, typed on Microsoft Word 95 together with a
diskette.
Yours sincerely.
Dr.
Sevil Atalay Vural
Enclosed:
1.
Two copies of the manuscripts
2.
Six figures
3.
One diskette