Pulmonary Pathological Features in Viraemia Associated Secondary Lung Injury
Hranush Arzumanyan1, Tigran Mezhlumyan2, Nazeli Gevorgyan2, Alexander Karalyan2, Aida Avetisyan1,3 and Sona Hakobyan1*
1Laboratory of Cell Biology and Virology, Institute of Molecular Biology of NAS RA, Armenia
22Yerevan State Medical University, Armenia
3Experimental laboratory, Yerevan State Medical University, Armenia
Submission: April 23, 2021; Published: May 19, 2021
*Corresponding author: Sona Hakobyan, Laboratory of Cell Biology, Institute of Molecular Biology of NAS RA, Armenia
How to cite this article: Hranush A, Tigran M, Nazeli G, Alexander K, Aida A, et al. Pulmonary Pathological Features in Viraemia Associated Secondary Lung Injury. Int J Pul & Res Sci. 2021; 5(1): 555652. DOI: 10.19080/IJOPRS.2021.05.555652
Abstract
Both African swine fever virus (ASFV) and Rabbit hemorrhagic disease virus (RHDV) are important pathogens in veterinary. ASFV causes African swine fever (ASF) in pigs and RHDV causes rabbit hemorrhagic disease (RHD) in rabbits. Secondary lung pathology was investigated for these diseases as one of the consequences of viraemia. Rabbits and pigs were taken for the observation of these diseases. Imprint smears of the lungs, lung tissue and blood samples from intact and infected animals were taken for the exploration. Afterwards, some observations were done for each animal: histopathological analysis of lungs, bronchoalveolar lavage (BAL) cell population counting and detection of serum TNF-alpha, IFN-gamma and NO levels. Histopathological analysis showed many hemorrhages in lung tissue. BAL analysis presented significant changes in cell population. Serum levels of TNF-alpha, IFN-gamma and NO were increased. From the results can be concluded, that there are many similarities in the secondary lung pathology for these viruses and the main mechanism of lung tissue pathology is the high vascular permeability caused by changes in cytokines and NO levels.
Keywords: African swine fever virus; Rabbit hemorrhagic disease virus; BAL cells; Lung pathology; Hemorrhages
Abbreviations: BAL: Broncoalveolar Lavage; AM: Alveolar Macrophages; ASFV: African Swine Fever Virus; RHDV: Rabbit Hemorrhagic Disease Virus; DPI: Days Post Infection; DIC: Disseminated Intravascular Coagulation
Introduction
African swine fever virus (ASFV) is a double-strained DNA virus and is classified as the only member of the family Asfarviridae. ASFV causes African swine fever (ASF) which is one of the most important threats in pig breeding and wild boar populations because of high mortality [1-3]. The replication of ASFV takes place mainly in monocytes and macrophages [4]. Proinflammatory cytokines (ILs, TNF- alpha, IFN- gamma) and NO produced by infected monocytes and macrophages are playing an important role in the pathogenesis of this disease causing an immoderate inflammatory response and inducing the apoptosis of macrophages and lymphocytes [5,6]. The consequences are hemorrhages in various organs.
Rabbit hemorrhagic disease virus (RHDV) is a linear positive-sense RNA virus of family Caliciviridae [7]. RHDV causes the rabbit hemorrhagic disease (RHD), also known as rabbit plague. RHD is characterized by necrotizing hepatitis, but hemorrhages may also can be detected in other organs, particularly in the lungs, heart and kidneys [8]. In earlier studies it was presented that the host cells for RHDV are hepatocytes and mononuclear phagocytes [9]. As well as for ASFV, it was shown serum levels elevation of TNF-alpha and IFN-gamma for RHDV [7].
The predominant pathological findings in lung injury caused by investigated viruses are lung hemorrhages. These severe pulmonary injuries of investigated animals can be caused both by direct viral effects by abnormal immune response [6,8]. Till now many important aspects of the lung pathology and pathogenesis of ASF and RHD have not yet been fully clarified. The goal of this study was to investigate effect of RHDV and ASFV on host lungs by analysis of bronchoalveolar lavage cell populations, histopathologic observation of lung tissues and examination of serum levels of NO, TNF-alpha and IFN-gamma. The mechanisms of lung pathologies in both the diseases are also being compared.
Methods
Viruses
For the investigations it was used ASFV (genotype II) distributed in the Republic of Georgia and the Republic of Armenia. Infectious titer of ASFV was calculated by the method of haemadsorption [10]. RHDV was obtained from Agricultural University of Armenia. The virus sample was prepared from infected rabbit livers. HA test and PCR was used for routine diagnosis of RHD [11]. The hemagglutination test was performed according to Nystrom et al. [12].
Animals
15 pigs of the same age (3 months old) and weight (30-32kg) were used for infection (n=12) and as controls (n=3). The animals were housed in separate stables, where they had access to a commercial feed twice per day and to clear water at all times. Pigs were intramuscularly inoculated in the hip with 5ml of 104 50% hemadsorbing doses (HAD50)/ml doses of the Georgia 2007 isolate. Nine (n=9) pigs were used for tissue sampling and cell analysis, whereas three other pigs (n=3) were used to collect blood and cytokine experiments. The viral titer in sera was determined by hemadsorption microtest and expressed as log 10 HAD50/ml.
Twelve rabbits (Oryctolaguscuniculus), 6 months old with an average weight of 2.0kg, were purchased from a conventional rabbitry. All rabbits were RHDV-negative. Absence of RHDV antibodies in rabbit blood sera was demonstrated by hemagglutination inhibition test, and PCR reaction. Nine rabbits were inoculated intramuscularly with 1ml each of a 10% liver homogenate, and 3 rabbits served as control [13].
Imprint smears and AM number
Imprint smears were obtained from the fresh cut surface of lung after autopsy, fixed routinely in 95% ethanol, and then stained using the Papanicolaou technique. The imprint smear slides (n=5) in each case were examined by 3 observers and assessed for the number of macrophages per field 70×54µm. In each examination were observed 100 fields. Active AM were detected using following criteria: increased phagocytosis, vacuolization of the cytoplasm and arising of pseudopodia [14].
Histopathology
Tissue samples of buffered formalin fixed lungs were dehydrated, embedded in paraffin wax, sectioned at 5µm, and stained with haematoxylin and eosin for microscopic evaluation.
Cytokine analysis
From 1 to 3 days post infection (dpi), blood samples were collected from the ophthalmic venous sinuses of pigs as described by Stier and Leuch19. In rabbit preinoculation (0 dpi) blood samples were taken as control values. Blood samples were drawn by heart puncture in each case from 3 rabbits. ELISA method was used to detect the serum levels of TNF-alpha, IFN-gamma in the culture supernatants (Mybiosource). The levels of cytokines (pg/ml) were measured using a colorimetric reader (Stat Fax 303 Plus) and were calculated according to the cytokine standard curve supplied in the kits. All samples were tested in duplicate according to manufacturers’ instructions.
Determination of NO
Griess method was used for determining NO levels. 1% Sulfanilamide in 5% H3PO4 (aqueous) and 1% N-naphthyl-ethylenediamine (aqueous) was premixed to form a 200µl NO production was evaluated by a colorimetric assay for the nitrite metabolite based on the Griess reaction. Minor changes were made to the common procedure. Briefly, on 1.5ml of deoxygenated distillated water 200µl of supernatant was reacted in a mixture of 100µl of 0.1% N-naphthyl-ethylenediaminedihydrochloride (NED) and 100µl of 1.0% sulphanilamide in 5.0% phosphoric acid at room temperature. The 2 parts were mixed within 12h of use and kept chilled (+4°C). The absorbance was read after 15 minutes in a spectrophotometer at 540nm with reference to a standard nitrite quantitative curve with a maximum concentration of 3mm. Deoxygenated distillated water was used to avoid nitrite oxidation.
Statistical analysis
All experiments were repeated 3 times and statistical analyses were performed using the Student’s t test. SPSS version 13.0 software package (SPSS Inc., Chicago, IL, USA) was used for statistical analyses.
Results
Lung histopathology
Experimental animals were infected by intramuscular injection by viruses (ASFV and RHDV). In both cases were observed standard course of the diseases; fever commenced several hours after the viraemia which were detected after 24 hours post infection (hpi). Lung pathology investigated in 72hpi.
As shown in (Table 1), after the viraemia significantly increased the amount of lymphocytes and neutrophils in bronchoalveolar lavage (BAL). Both infections ASFV (at 3-5dpi) and RHDV (at 2-3dpi) caused pulmonary hemorrhage. By RHDV hemorrhages in lung tissue were more prominent and intensive (Figure 1A) compared to ASFV induced lesions (Figure 1B).
After 48-72 hpi BAL investigation showed intense alveolar inflammation, with recruitment of inflammatory cells, predominantly lymphocytes and neutrophils (Table 1, Figure 1C & 1D). Also, were observed massive diapedesis of erythrocytes, neutrophils, and lymphocytes in lung tissue of infected rabbits (Figure 1C & 1E). These processes were accompanied by increased number of all types of cells in alveolar cavities of pigs (Figure 1D & 1F). All above mentioned suggest an increase in the permeability of the wall of the alveoli.
Cytokines levels in serum
It has been detected, that viraemia in both cases (RHDV and ASFV) was associated with increased levels of IFN gamma (Figure 2A & 2B) and TNF alpha (Figure 2C & 2D) in serum of infected rabbits as well as pigs.
It can be seen from (Figure 2A), that Rabbit IFN-gamma levels has been elevated since 1st dpi. The same results have been detected for Porcine IFN-gamma levels (see Figure 2B). In case of Rabbit TNF-alpha levels, it has been evaluated elevation since 2nd dpi andin case of Porcine TNF-alpha levels has been increased since 1st dpi. Thus, in all cases significant changes has been detected compared with control/ 0 dpi.
Nitric oxide
Our study demonstrated that both in rabbits and in pigs with the viraemia were observed significantly higher serum levels of NO than in healthy animals (Figure 3). According to our results, serum levels of nitric oxide have been increased in both cases of diseases. Furthermore, in infected rabbits’ elevation was detected since 1st dpi, and in infected pigs since 2nd dpi (see Figure 3).
Discussion
It has been shown above gross postmortem findings revealed lung hemorrhages. The hemorrhages, diapedesis and the increase in the lymphocyte and neutrophil amount in BAL indicate the development of significant pulmonary pathology. In both infections, the lungs do not become the primary target for viral infections but are susceptible to secondary viral invasions resulting from the viremia [6,8]. The cells of the mononuclear phagocyte system are involved in the pathogenesis of RHD and ASF, and a significant role are playing proinflammatory cytokines and NO produced by these cells.
Data of Trzeciak-Ryczek et al. [15] and Semerjyan et al. [7] for both ASFV and RHDV it was shown increase of serum TNF-alpha and IFN-gamma levels. In our research we detected similar results: starting from 1 dpi there are significantly high TNF-alpha and IFN-gamma concentrations in serum. Furthermore, we have found increased serum NO levels since the 1 dpi in both cases. IFN-gamma has antiviral activity and chemotactic effect on monocytes/macrophages [16]. It induces the synthesis of TNF-alpha contributing its high levels [15]. TNF-alpha is considered to be the main mediator of programmed cell death [17].
It induces the apoptosis of uninfected lymphocytes in ASFV-infected pigs causing lymphopenia and severe impairment of lymphoid organs [18], and in hepatocytes of RHDV-infected rabbits leading to liver damage and dysfunction [19]. Also, it is well-known that TNF-alpha is an important mediator in the regulation of endothelial permeability [20]. TNF-alpha causes vasodilation, increases the vascular permeability, leads to elevation of the tissue factor expression and detraction of trombomodulin expression thereby inducing indirectly disseminated intravascular coagulation (DIC) [16]. The severe liver necrosis in RHD is also a contributing factor in the manifestation of DIC.
In past research it was shown that high NO levels have role in increasing of permeability of capillaries. From this fact it seems that the path of pathogenesis in lungs is similar for both viruses. Probably the high NO level is side effect of the macrophage striving against virus-NO is one of the mediators in intracellular inhibition of viral replication. From recent studies we know for ASF that NO elevates the endothelial permeability mediated by vascular endothelial growth factor [6]. It seems that this mechanism of a diapedesis exists for RHD too.
The lung pathology is similar in both diseases and is presented with diapedesis. We can surely affirm that some pathological mechanisms resemble as follows: vascular permeability mediated by TNF-alpha and also probably by NO-stimulated VEGF, target cells apoptosis and disseminated intravascular coagulation causing hemorrhages [6-8,19,20]. Another common feature is the high concentration of IFN-gamma. For RHD an additional contributing factor in the lung pathology is the liver necrosis [19]. So, we can conclude that lung pathology seen in animals with both viruses shows marked microvascular thrombosis and hemorrhage linked to extensive alveolar, diapedesis and interstitial inflammation that shares features with macrophage activation syndrome.
Conclusion
From the results can be concluded, that there are many similarities in the secondary lung pathology for these viruses and the main mechanism of lung tissue pathology is the high vascular permeability caused by changes in cytokines and NO levels.
Ethical Statement
All animal experiments were permitted by the Institutional Review Board/Independent Ethics Committee of the Institute of Molecular Biology of NAS RA (reference number IRB00004079).
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