CC BY
9
The Effect of a Lipopolysaccharide from Rhodobacter capsulatus PG on Inflammation Caused by Various Influenza Strains
S. V. Zubova1*, M. F. Vorovich2,3, A. S. Gambaryan2, A. A. Ishmukhametov2,3, S. V. Grachev1,3, I. R. Prokhorenko1
institute of Basic Biological Problems of RAS, FRC PSCBR RAS, Science Ave. 3, Pushchino, Moscow, 142290, Russia
2FGBNU Federal Scientific Center of Research and Development of Immunobiological Preparations named M.P. Chumakov of RAS, pos. Institute of Poliomyelitis, Kievskoye Highway, 27th km, 8/1, Moscow Region, 142782, Russia
3GAOUVO First Moscow State Medical University named I.M. Sechenov of Russia Health Ministry, Trubetskaya Str. 8, Moscow, 119811, Russia *E-mail: zusvet@rambler.ru
Received December 5, 2018; in final form, May 15, 2019 DOI: 10.32607/20758251-2019-11-3-46-55
Copyright © 2019 National Research University Higher School of Economics. This is an open access article distributed under the Creative Commons Attribution License,which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
ABSTRACT The development of a specific inflammation in mice that had been infected by two influenza virus strains, A/chicken/Kurgan/5/2005 (H5N1) and A/Hamburg/2009 MA (H1N1), was studied. We investigated the effect of a non-toxic lipopolysaccharide from Rhodobacter capsulatus PG on the survival and body weight of the mice, production of IgG antibodies, and the induction of pro- and anti-inflammatory cytokines in blood serum. The administration of the R. capsulatus PG lipopolysaccharide was shown to induce interferon-P synthesis, both in healthy and influenza A virus-infected mice, and to promote production of antiviral antibodies in the blood of the influenza-infected animals.
KEYWORDS influenza virus, H5N1, H1N1, Rhodobacter capsulatus PG lipopolysaccharide, mice, antiviral antibodies, cytokines.
ABBREVIATIONS DAMP - damage-associated molecular pattern; HA - hemagglutinin; HMGB1 - high mobility group box 1 protein/amphoterin; IFN - interferon; Ig - immunoglobulin; IL - interleukin; MD-2 - myeloid differentiation protein 2; MDCK cells - Madin-Darby canine kidney cells; MyD88 - myeloid differentiation protein 88; NP - nucleoprotein; PA, PB1 - polymerase complex proteins; TLR - Toll-like receptor; TNF - tumor necrosis factor; TRAF6 - TNF receptor-associated factor 6; ELISA - enzyme-linked immunosorbent assay; LPS - lipopolysaccharide.
INTRODUCTION
Influenza epidemics have, to date, affected millions of people across the world despite the use of recommended vaccines, whose effectiveness proves lower than expected [1, 2]. Influenza A viruses have a high degree of genomic variation and produce resistant strains that can be controlled by vaccines or antiviral systemic medication for some time. The development of safe and effective vaccines remains an important public health goal.
The interaction of viral components with various receptors activates the intracellular pathways responsible for the secretion of type I IFN, pro-inflammatory
cytokines, and chemokines. The key factors involved in the recognition of viral ligands are the Toll-like receptors (TLRs) of innate immune cells. TLR2 and TLR4, situated on the cell surface, recognize viral envelope glyco/lipoproteins, while intracellular endosomal TLR3, TLR7, TLR8, and TLR9 recognize nucleic acids [3, 4]. Toll-like receptors can interact with other receptors, thereby stimulating the response of innate immune cells to pathogens, including influenza viruses [4]. TLR4 can be activated by damage-associated molecular patterns (DAMPs), which are molecular structures released by virus-infected cells [5]. Different influenza strains activate cells through various mechanisms,
which lead to the synthesis of various cytokines and chemokines [6, 7].
Compound E5564 (Eritoran), a synthetic analogue of the non-toxic lipid A from Rhodobacter sphaeroides, when administered in a certain regimen to C57BL/6J mice, was shown to protect mice from death caused by the mouse-adapted H1N1 influenza virus [8]. The nuclear non-histone high mobility group box 1 (HMGB1) protein/amphoterin, which is a DAMP, is known to be released relatively late after the infection onset and is involved in the development of both gram-negative sepsis and influenza complications, interacting with MD-2 and activating TLR4 [5, 9, 10]. TLR4 activation leads to a cytokine storm with an accentuated release of pro-inflammatory cytokines, including interferons, tumor necrosis factors, interleukins, and chemokines [11]. Pharmacological blockade of TLR4 by Eritoran can significantly reduce mouse mortality from avian influenza [8]. A lipopolysaccharide (LPS) from a pho-totrophic bacterium R. capsulatus PG (Rb.) strain [12], with a lipid A structure similar to that of lipid A from R. sphaeroides, is an endotoxin antagonist that inhibits activation of the synthesis of numerous pro-inflammatory cytokines by human blood cells [13], an indication of its ability to block TLR4.
Mice are the main tools used for studying the human immune system and immune responses. However, there are significant differences between the innate and adaptive immune systems of mice and those of humans, which reside in the blood cell ratio, plasma composition, surface receptors, the expression levels of various cytokines and chemokines, etc. [14, 15]. This should be considered when using mice as human disease models.
In this paper, we studied the effect of a non-toxic Rb. LPS on the induction of pro- and anti-inflammatory cytokines and survival rates of mice infected with various influenza A strains. The study aim was to investigate the features of the inflammatory processes caused by H1N1 and H5N1 influenza viruses.
Hamburg/2009 MA (H1N1). Viruses were cultured in chicken embryos. The virus median tissue culture infectious dose (TCID50) was determined by titration in a Madin-Darby canine kidney (MDCK) cell culture. The median lethal dose (LD50) was determined by titration in mice. Experiments with the highly pathogenic A/ chicken/Kurgan/5/2005 virus were performed in boxes with the BSL-3 safety level.
Mice
We used 10-14 g Balb/c mice, 36-38 days of age, regardless of gender. The animals originated in the nursery of the Scientific Center for Biomedical Technology of the Federal Medical and Biological Agency. All manipulations with the animals were performed according to the Rules of Laboratory Practice in the Russian Federation [17], in compliance with biological ethics in experiments on laboratory animals.
Experimental influenza infection in mice infected with the influenza virus strain H5N1
Mice were divided into six groups depending on the received drugs. Each group included at least 12 animals. The animals in the five groups were infected, under light ether anesthesia, intranasally (50 ^L each) with the highly pathogenic avian influenza virus H5N1 at doses of 10 to 105 TCID50 per mouse, which amounted to 10-1 to 103 LD50. The sixth control group remained uninfected. After 24 h, all groups were divided in half. One half of the animals was injected intraperitoneally with 500 ^L/mouse of saline daily for the following 4 days, and the other half was injected with the Rb. LPS at a dose of 400 ^g/500 ^L/mouse. Mice not injected with any agents were the controls. The experimental design is shown in Fig. 1. Blood was sampled from the animals that survived by the end of the experiment (day 14), after euthanasia in a CO2 chamber; blood cells were precipitated; and the resulting serum was frozen at -20°C until the H5N1 influenza virus antibody titer in the serum was determined by ELISA.
EXPERIMENTAL
The following ELISA kits were used: mouse TNF alpha platinum ELISA, mouse IL-6 platinum ELISA, mouse IL-10 platinum ELISA, and mouse INF gamma platinum ELISA (eBioscience, USA), as well as a mouse IFN beta ELISA kit (PBL Assay Science, USA).
The Rb. LPS was produced in a laboratory of the Institute of Basic Biological Problems, according to the procedure described previously [16].
Viruses
We used the following influenza A virus strains: chicken/Kurgan/5/2005 (H5N1) and mouse-adapted
Experimental influenza infection in mice infected with the mouse adapted influenza virus strain H1N1
The mice-adapted pandemic virus H1N1 used in the study was passed serially 20 times in a mouse lungs and differed from the parent A/Hamburg/2009 (H1N1) strain by a deletion in neuraminidase (NA) and mutations in the HA, NP, PA, and PB1 proteins (Table). The H1N1 influenza virus is 105-fold more pathogenic for mice compared to the initial parent strain.
The mice were divided into three groups depending on the received drugs. Each group included at least 12 animals. Two groups of mice were infected, under mild ether anesthesia, intranasally (50 ^L each) with the
Day 0: intranasal infection (50 pL) with the H5N1 virus in different dilutions (from 10 to 105 TCID50) under ether anesthesia
10-14 g Balb/c mice, 36-38 days of age, regardless of gender
Day 14
10
t
11
-I—
12
—I—
13
14
0
1
Intraperitoneal injection of the LPS from R. capsulatus PG (400 pg/500 pL) or saline (500 pL) daily
Fig. 1. Design of the experiment on the infection of mice with the A/chicken/Kurgan/5/2005 (H5N1) influenza virus strain
Day 0: intranasal infection (50 pL) with the H1N1 virus in dilutions 10 and 300 TCID50 under ether anesthesia
10-14 g Balb/c mice, 36-38 days of age, regardless of gender
t
4
t i
T"
10
Day 12
11
12
0
1
2
Intraperitoneal injection of the LPS from R. capsulatus PG (400 pg/500 pL) or saline (500 pL) daily
Fig. 2. Design of the experiment on the infection of mice with the A/Hamburg/2009 MA (H1N1) influenza virus strain
Substitutions in the A/Hamburg/2009 virus during adaptation to mice
Viral strain Viral protein, amino acid sequence
NA HA NP PA PB1
56-67 158 224 225 289 92 317
Hamburg/2009 G R D H N M
Hamburg/2009 MA Del 56-67 E K G Y S V
mouse-adapted H1N1 influenza virus at doses of 10 and 300 TCID50 per mouse. The control group included un-infected mice. Two days after infection, all groups were divided in half. One half of the animals was injected intraperitoneally with 500 pL/mouse of saline daily for the following 4 days, and the other half was injected with the Rb. LPS at a dose of 400 pg/500 pL/mouse. Mice not injected with any agents were the controls. The experimental design is shown in Fig. 2. Five hours after administration of the Rb. LPS, blood was sampled in three mice from each group, after euthanasia in a CO2 chamber, on days 3, 4, and 5. The blood was cen-trifuged, and the resulting serum was frozen at -20 °C until the cytokine levels were determined by ELISA. Blood was sampled from the animals that had survived by the end of the experiment (day 14), after euthanasia in a CO2 chamber; blood cells were precipitated, and the resulting serum was frozen at -20 °C until the serum levels of the H1N1 influenza virus IgG1 and IgG2a antibodies were determined by ELISA.
Determining Cytokine Levels
Levels of TNF-a, IL-6, IL-10, IFN-y, and IFN-P cytokines in the blood serum of mice infected with the H1N1 influenza virus were determined using ELISA kits according to the manufacturer's recommended procedure. The optical density of the samples was measured using a STAT FAX 3200 immunoassay analyzer (Awareness, USA) at a wavelength of 450 nm.
Determining influenza virus antibody levels
To determine the levels of antibodies to hemagglutinin (HA) of the H5N1 and H1N1 influenza viruses in the serum of the mice, allantoic fluid containing 64 HA units of one of the viruses was added to a plate sensitized with fetuin, kept at 40°C overnight, washed with phosphate-buffered saline (PBS) pH 7.4 with 0.1% Tween-20, and blocked with buffer A (0.1% Tween-20, 0.2% BSA in PBS) for 1 h. To determine the IgG1 and IgG2a antibodies, each serum sample was titrated on two different plates. The blocking solution was removed, and wells were added with 100 pL of the serum from H5N1-infected mice at 1 : 40 to 1 : 2,560 dilutions or from H1N1-infected mice at 1 : 50 to 1 : 3,200 dilutions in buffer A. Plates were incubated at 40°C for 4 h, washed with PBS, added with horseradish perox-idase-labeled rabbit antibodies against mouse immu-noglobulins (Sigma, USA) or against mouse IgG1 or IgG2a, and incubated at 40°C for 2 h. Then, the plates were washed with PBS and stained with ortho-phe-nylenediamine. The optical density of the samples was measured using an AIFR-01 Uniplan immunoassay analyzer (Picon, Russia) at a wavelength of 492 nm. Control wells without viral particles were used to ex-
clude nonspecific binding. The antibody level in the samples was expressed as serum dilution enabling a signal exceeding twice the background value.
Statistical analysis
Microsoft Office Excel 2010 (AtteStat plugin) and Orig-inPro 7.5 were used for statistical analysis and graphical presentation of our data. Statistically significant differences between the results were evaluated using a nonparametric Mann-Whitney U-test. Differences were considered significant at a significance level p < 0.05.
RESULTS AND DISCUSSION
The condition of the experimental animals was evaluated based on survival and body weight changes. The administration of the Rb. LPS into the control mice, as well as infection with a minimum dose of 10 TCIDc„ of
50
the H5N1 virus, regardless of Rb. LPS administration, did not affect the survival rates of the animals up to the end of the experiment (day 14) (Fig. 3). Deaths of animals in the groups infected with doses of 102/103 and 104/105TCID50 of the H5N1 virus began on days 8 and 6 after infection, respectively. All mice that had received 103, 104, and 105 TCIDc„ of the influenza virus
50
died by day 10 after the infection, regardless of Rb. LPS administration. Additional administration of the Rb. LPS to mice infected with the influenza virus at a dose of 102 TCID50 increased their mortality (Fig. 3). The curves of weight changes revealed that introduction of the Rb. LPS into healthy animals did not affect their condition and weight (Fig. 4). Mice infected with 10-102 TCID50 of the virus continued to gain weight throughout the experiment. Infection with doses of 103-105 TCID50 significantly affected the condition of the animals, causing significant inflammation and rapid weight loss. Additional administration of the Rb. LPS to infected animals led to even greater weight loss (Fig. 4).
The administration of the Rb. LPS to the control mice and infection with a dose of 10 TCIDc„ of the H1N1
50
influenza virus, followed by the administration of the Rb. LPS, did not affect the survival rate of the animals until the end of the experiment (day 12). In the group of mice infected with the influenza virus at a dose of 300 TCID50, 14% of the mice survived until the end of the experiment; additional administration of the Rb. LPS increased mortality in mice (Fig. 5). An analysis of weight change curves showed that the administration of the Rb. LPS to healthy mice did not affect the condition and weight of the control animals. Mice infected with 10 TCID50 of the H1N1 virus showed no signs of disease and began rapidly gaining weight on the 3rd day after infection, until the end of the experiment (day 12). Additional administration of the Rb. LPS to
80
--s
60
ra
I 40
□
on
20
160 -, 150 -140
¡g 130
m
H 120
-c 110
"<u
£ 100 9080 70
—< < ^
—►
—►
~1-1-1-r-
-1-1-1-1-1-1-r
0 2 4 6 8 10 12 14 Time, days
4
—r 6
—r~ 8
10
12
14
C
C + Rb. LPS 10 TCID50
10 TCID50 + Rb. LPS 102 TCID50
102 TCID50 + Rb. LPS
103 tcid50
103 TCID^ + Rb. LPS
104 tcid50
104 TCID^ + Rb. LPS
105 TCID50
105 TCIDin+ Rb. LPS
C
C + Rb. LPS 10 TCID50
10 TCID50 + Rb. LPS
102 тaD5n
102 TCID^ + Rb. LPS
103 tcid^
103 TCID^ + Rb. LPS
104 tcid5()
104 TaD5() + Rb. LPS
105 TaD5()
105 TCID^ + Rb. LPS
Fig. 3. Survival of mice in response to the administration of the Rb. LPS, A/chicken/Kur-gan/5/2005 (H5N1) influenza virus, and both factors simultaneously
Fig. 4. Weight changes in mice in response to the administration of the Rb. LPS, A/chick-en/Kurgan/5/2005 (H5N1) influenza virus, and both factors simultaneously
Time, days
the animals infected with the virus at this dose led to a decrease in the animals' weight after day 7 of the experiment. Virus infection (300 TCID50) markedly affected the condition of the mice, causing significant inflammation and weight loss. The administration of the Rb. LPS to infected mice worsened the condition of the animals and led to additional weight loss (Fig. 6).
Survival and weight changes in the animals infected with the H5N1 or H1N1 influenza virus revealed the absence of a protective effect on the part of the Rb. LPS on mice against a lethal infection (Fig. 3-6). Daily
(for 5 days) intravenous administration of Eritoran starting 2 days after infection was shown to protect mice from the A/PR/8/34 (H1N1) influenza virus. Protection from DAMPs released from influenza infected and destroyed cells that occurred through the TLR4-dependent mechanism [18]. The virus type determines the response mechanisms of innate immunity to infection. The signaling pathways in an infection caused by different H5N1 and H1N1 virus strains differ and determine the survival rate and pathology of the inflammation [7]. Obviously, the infection in our experiments
0
--s
15 >
> □
on
cr-
<u m c ra
'<u
100-
80-
60
40
20
140 n 135 -130125 -120115110105 -10095 : 9085 80 7570-
->—I-
-A—■*
0 2 4 6 8 10 12 Time, days
10
—r~ 12
Fig. 5. Survival of mice in response to the administration of the Rb. LPS, A/Ham-burg/2009 MA (H1N1) influenza virus, and both factors simultaneously
Fig. 6. Weight changes in mice in response to the administration of the Rb. LPS, A/ Hamburg/2009 MA (H1N1) influenza virus, and both factors simultaneously
Time, days
develops through molecular mechanisms other than cell activation through the TLR4 pathway. Probably, the administration regiment and Rb. LPS concentration used in our experiments were ineffective in protecting against these viral strains.
Signs of viral infection include an increased induction of pro-inflammatory cytokines and chemokines, such as TNF-a, IL-1, IL-6, IL-8 [19], as well as IFN-0 and IFN-y, which have antiviral effects [20, 21].
The administration of the Rb. LPS to mice caused a 1.5-fold increase in the TNF-a level in blood serum compared to that in the control mice by day 3, which
remained at about the same level until day 5 of the experiment. It should be noted that the serum TNF-a level in the control mice was quite high (74.7 ± 8.7 pg/mL), indicating a sensitized state of the animals. Production of TNF-a in the blood of the influenza-infected mice depended on the virus dose and showed positive dynamics during the experiment. The administration of the Rb. LPS to infected mice enhanced TNF-a production in their blood (Fig. 7A).
The dynamics of IL-6 synthesis in all experiment variants was similar. The IL-6 level increased significantly (1000- to 2000-fold) by day 4 of the experiment.
0
2
4
8
250 200
C
100 50 0
50 0
E 80 60
An
a 40
20
-r-C
C
Day 3
Day 3
Day 4
Day 4
Day 5
Day 5
B 24002000
_i 1600
£
^1200-800 400 0
D
150-
a.
100-
50
—r~
C
C
Day 3
Day 4
Day 5
Day 3
Day 4
Day 5
C
Day 3
Day 4
Day 5
Fig. 7. Dynamics of cytokine levels in response to the administration of the Rb. LPS, A/Hamburg/2009 MA (H1N1) influenza virus, and both factors simultaneously. A - TNF-a, B - IL-6, C - IL-10, D - IFN-y, E - IFN-ß
0
IL-6 production in the infected mice depended on the virus dose. The IL-6 level in response to the introduction of the Rb. LPS was comparable to that in the influenza-infected mice. The administration of the Rb. LPS to infected mice slightly increased IL-6 production by day 5 of the experiment (Fig. 7B).
These findings demonstrate that a viral infection causes a dose-dependent induction of the synthesis of the pro-inflammatory cytokines TNF-a and IL-6, with the induction increasing with time. These cytokines are produced mainly by monocytes and macrophages in response to both bacteria and viruses, using independent
0.6^
0.5
0.4H
0.3
0.2H
0.1
100
Serum dilution
Fig. 8. Effects of the Rb. LPS on the levels of antibodies to the A/chicken/Kurgan/5/2005 (H5N1) influenza virus in the serum of mice survived by day 14 of the experiment. A - virus dose of 10 TCID50; B - virus dose of 102 TCID50; C - antibody titer in relative units. ***p < 0.001
B
signaling pathways involving different surface and intracellular receptors but the same adapter proteins and transcription factors. The data on the induction of TNF-a and IL-6 synthesis show that the administration of the Rb. LPS to influenza-infected mice enhanced the pro-inflammatory response of their immune cells (Fig. 7A, B). This worsened the condition of the animals, as evidenced by the data on the survival rate and weight changes (Fig. 5, 6).
The administration of the Rb. LPS into mice caused an increase in the anti-inflammatory IL-10 cytokine level that exceeded the baseline level 3-fold by day 5. The influenza virus, regardless of the dose, had no effect on the production of the anti-inflammatory IL-10 cytokine. The administration of the Rb. LPS into infected mice, regardless of the virus dose, had almost no bearing on the induction of IL-10 synthesis compared to the administration of the Rb. LPS alone (Fig. 7C). The immunoregulatory cytokine IL-10 is a key component of the system that regulates excessive
immune responses by suppressing the expression of pro-inflammatory cytokines such as TNF-a, IL-6, and IL-1 [22, 23]. Levels of IL-10 production in response to LPS are significantly higher than those in a viral infection [24, 25]. The obtained results indicate an increase in the IL-10 level in response to the administration of the Rb. LPS into both healthy and influenza-infected mice. This may indicate that the Rb. LPS promotes enhanced anti-inflammatory responses by cells (Fig. 7C).
These findings indicate a lack of IFN-y production in response to the administration of the Rb. LPS to mice. The influenza virus increases the blood IFN-y level in mice in a dose-dependent manner. Furthermore, additional administration of the Rb. LPS to mice infected with the H1N1 influenza virus reduced IFN-y production in their blood (Fig. 7D).
Having no effect on the production of IFN-y, the Rb. LPS caused a 4-fold increase in the IFN-P production compared to the control level by day 4 of the experiment. On day 5, the IFN-P level had decreased to its
0.6 0.5H 0.4 0.30.20.1 -0.0
C
10
0.6 0.5 0.4 0.3 0.2 0.1 0.0
10
2 1
18000 16000 14000 12000 10000 8000 6000 4000 2000
—i-1-1—I—i—i i i i-1-1-1—i—i—i i i i-
100 1000
100 1000 Serum dilution
10 TCID50 10 tcid50 + Rb. LPS
+ Rb. LPS
Fig. 9. Effects of the Rb. LPS on the levels: A - IgG1 and B - IgG2a antibodies to the A/Hamburg/2009 MA (H1N1) influenza virus (virus dose of 10 TCID50) in the serum of mice survived by day 12 of the experiment. C - titer of IgG antibodies in relative units. *p < 0.05
*
3
0
B
3
2
baseline value. In response to a H1N1 virus infection at a dose of 10 TCID„, the IFN-P level increased 3-fold
50
by day 5 of the experiment. The influenza virus at a dose of 300 TCID50 significantly increased the induction of IFN-P (16-fold), compared to the baseline value by day 4. The administration of the Rb. LPS to mice infected with 10 TCID„ and 300 TCID„ of the influenza
50 50
virus enhanced or decreased, respectively, the cytokine level, compared to that in mice infected with the influenza virus alone (Fig. 7E).
These results demonstrated that the levels of IFN-y and IFN-P synthesized in response to the used Rb. LPS administration schedule were insufficient for an effective antiviral protection against the virus strains under study.
IFN-P, a component of the influenza vaccine, acts as a powerful adjuvant and helps induce the synthesis of IgG2a and IgA, providing protection against infection. Production of IgG2a antibodies, which is characteristic of the response to a viral infection, has a protective and neutralizing effect against influenza viruses. Expres-
sion of type I IFN and generation of IgG2a antibodies in a viral infection are interrelated events of biological significance for subsequent protective immunity [26].
The action of existing vaccines against an influenza virus infection is based mainly on the induction of neutralizing antibody synthesis in response to viral HA [27]. Determination of the level of H5N1 virus HA antibodies in mouse serum revealed that the higher the infective virus dose, the higher the titer of serum antibodies in the infected animals. Additional administration of the Rb. LPS to H5N1-infected mice resulted in a significant increase in the antibody titer (p < 0.001) in blood serum
(Fig. 8).
Determination of IgG1 and IgG2a antibody levels in response to the H1N1 virus infection showed that IgG2a titers were significantly higher than the IgG1 titers in all the groups of animals. Introduction of the Rb. LPS statistically significantly increased the serum IgG2a level compared to influenza-infected mice without additional administration of the Rb. LPS (p < 0.05) (Fig. 9).
The innate immune response is crucial in the fight against viruses and plays a key role in the induction and regulation of adaptive immune responses. For this reason, TLR ligands are considered as potential adjuvants for inclusion in vaccines. Simultaneous delivery of a TLR ligand and an antigen of interest is believed to be more effective than vaccination with a mixture of an adjuvant and an antigen [28, 29].
Our findings demonstrate that the administration of the Rb. LPS to mice promotes IFN-ß production (Fig. 7E) or controls the blood IFN-ß level in mice infected with various doses of the influenza virus. IFN-ß promotes antibody production by acquired immunity cells [26]. Our findings also demonstrate that additional
administration of the Rb. LPS leads to the production of antibodies in the blood of animals infected with the influenza A virus (Fig. 8, 9).
CONCLUSION
Our study has demonstrated that the nontoxic natural Rb. LPS promotes the production of the immunomodulatory cytokine IFN-P both in healthy mice and in animals infected with influenza A/chicken/Kur-gan/5/2005 (H5N1) and A/Hamburg/2009 MA (H1N1) strains and also promotes the production of antibodies to the HA of these strains in the blood of infected animals.
REFERENCES
1. Pebody R., Warburton F., Ellis J., Andrews N., Potts A., Cottrell S., Johnston J., Reynolds A., Gunson R., Thompson C., et al. // Euro Surveill. 2016. V. 21. № 13. P. 30179.
2. McLean H.Q., Thompson M.G., Sundaram M.E., Kieke B.A., Gaglani M., Murthy K., Piedra P.A., Zimmerman R.K., Nowalk M.P., Raviotta J.M., et al. // J. Infect. Dis. 2015. V. 211. № 10. P. 1529-1540.
3. Finberg R.W., Wang J.P., Kurt-Jones E.A. // Rev. Med. Virol. 2007. V. 17. № 1. P. 35-43.
4. Kawai T., Akira S. // Immunity. 2011. V. 34. № 5. P. 637650.
5. Yang H., Antoine D.J., Andersson U., Tracey K.J. // J. Leu-koc. Biol. 2013. V. 93. № 6. P. 865-873.
6 Sakabe S., Iwatsuki-Horimoto K., Takano R., Nidom C.A., Le M.Q., Nagamura-Inoue T., Horimoto T., Yamashita N., Kawaoka Y. // J. Gen. Virol. 2011. V. 92. № 6. P. 1428-1434.
7. Leung Y.H., Nicholls J.M., Ho C.K., Sia S.F., Mok C.K., Valkenburg S.A., Cheung P., Hui K.P., Chan R.W., Guan Y., et al. // J. Gen. Virol. 2014. V. 95. № 9. P. 1870-1879.
8. Shirey K.A., Lai W., Scott A.J., Lipsky M., Mistry P., Plet-neva L.M., Karp C.L., McAlees J., Gioannini T.L., Weiss J., et al. // Nature. 2013. V. 497. № 7450. P. 498-502.
9. Wang H., Bloom O., Zhang M., Vishnubhakat J.M., Ombrel-lino M., Che J., Frazier A., Yang H., Ivanova S., Borovikova L., et al. // Science. 1999. V. 285. № 5425. P. 248-251.
10. Alleva L.M., Budd A.C., Clark I.A. // J. Immunol. 2008. V. 181. № 2. P. 1454-1459.
11. Liu Q., Zhou Y., Yang Z. // Cell Mol. Immunol. 2016. V. 13. № 1. P. 3-10.
12. Prokhorenko I.R., Grachev S.V., Zubova S.V. Patent for invention RU № 2392309 of 20.06.2010.
13. Kabanov D.S., Serov D.A., Zubova S.V., Grachev S.V., Prokhorenko I.R. // Biochemistry (Moscow). 2016. V. 81. № 3. P. 275-283.
14. Warren H.S., Fitting C., Hoff E., Adib-Conquy M., Beas-ley-Topliffe L., Tesini B., Liang X., Valentine C., Hellman J., Hayden D., Cavaillon J.M. // J. Infect. Dis. 2010. V. 201. № 2.
P. 223-232.
15. Munford R.S. // J. Infect. Dis. 2010. V. 201. № 2. P. 175-177.
16. Makhneva Z.K., Vishnevetskaya T.A., Prokhorenko I.R. // Prikladnaya Biokhimiya i Mikrobiologiya. 1996. V. 32. № 4. P. 444-447.
17. Order of the Ministry of Health of the Russian Federation No. 267 of 19.06.2003 «Rules of Laboratory Practice in the Russian Federation».
18. Shirey K.A., Lai W., Patel M.C., Pletneva L.M., Pang C., Kurt-Jones E., Lipsky M., Roger T., Calandra T., Tracey K.J., et al. // Mucosal. Immunology. 2016. V. 9. № 5. P. 11731182.
19. Mogensen T.H., Paludan S.R. // Microbiol. Mol. Biol. Rev. 2001. V. 65. № 1. P. 131-150.
20. Lai C., Wang X., Yang P. // Clin. Microbial. 2014. V. 3. № 3. P. 147-149.
21. Betakova T., Kostrabova A., Lachova V., Turianova L. // Curr. Pharm. Des. 2017. V. 23. № 18. P. 2616-2622.
22. Williams L., Bradley L., Smith A., Foxwell B. // J. Immunol. 2004. V. 172. № 1. P. 567-576.
23. Saraiva M., O'Garra A. // Nat. Rev. Immunol. 2010. V. 10. № 3. P. 170-181.
24. Yu X., Zhang X., Zhao B., Wang J., Zhu Z., Teng Z., Shao J., Shen J., Gao Y., Yuan Z., Wu F. // PloS One. 2011. V. 6. № 12. P. e28680.
25. Blok D.C., van der Sluijs K.F., Florquin S., de Boer O.J., van't Veer C., de Vos A.F., van der Poll T. // PloS One. 2013. V. 8. № 3. P. e58191.
26. Proietti E., Bracci L., Puzelli S., Di Pucchio T., Sestili P., De Vincenzi E., Venditti M., Capone I., Seif I., De Maeyeret E., et al. // J. Immunol. 2002. V. 169. № 1. P. 375-383.
27. Cox R.J. // Hum. Vaccin. Immunother. 2013. V. 9. № 2. P. 405-408.
28. Blander J.M., Medzhitov R. // Science. 2004. V. 304. P. 1014-1018.
29. Blander J.M. // Trends Immunol. 2007. V. 28. № 1. P. 19-25.
