43 research outputs found
Practices of Protest in the Conditions of the Developing Academic Capitalism
The article focuses on the problem of professional motivation of University teaching staff in the context of developing βacademic capitalismβ and presents the results of the empirical study carried out by the authors at the North-Western Institute of management of RANEPA in MarchβJune 2020. Based on the data obtained, it is revealed that teachers, experiencing deep deprivation of their social needs β the needs for respect, recognition and honor, are trying to find their place in the modern system, get out of the grip of double pressure, on the one hand, from the administration, which purposefully imposes rating systems and effective contracts, increasing competition between teachers, and on the other hand β students, who are now positioned as clients of universities. In the context of developing academic capitalism, teachers choose one of two adaptation strategies: 1) conformism as an opportunity to integrate into a constantly changing situation; 2) the practice of quiet protest as an opportunity to demonstrate the inefficiency of the entrepreneurial model of higher education, at least in its current version, and 3) neutral position to protect the classical values of the academic community
Protecting Mice from H7 Avian Influenza Virus by Immunisation with a Recombinant Adenovirus Encoding Influenza A Virus Conserved Antigens
Influenza is a highly contagious disease that causes annual epidemics and occasional pandemics. Birds are believed to be the source of newly emerging pandemic strains, including highly pathogenic avian influenza viruses of the subtype H7. The aim of the study: to evaluate the ability of the recombinant human adenovirus, serotype 5, which expresses genes of influenza A highly conserved antigens (ion channel M2 and nucleoprotein NP), to provide protection to laboratory mice against infection with a lethal dose of avian influenza virus, subtype H7. To achieve this goal, it was necessary to adapt influenza A virus, subtype H7 for reproduction in the lungs of mice, to characterise it, and to use it for evaluation of the protective properties of the recombinant adenovirus. Materials and methods: avian influenza virus A/Chicken/NJ/294508-12/2004 (H7N2) was adapted for reproduction in the lungs of mice by repeated passages. The adapted strain was sequenced and assessed using hemagglutination test, EID50 and LD50 for laboratory mice. BALB/c mice were immunised once with Ad5-tet-M2NP adenovirus intranasally, and 21 days after the immunisation they were infected with a lethal dose (5 LD50) of influenza virus A/Chicken/NJ/294508-12/2004 (H7N2) in order to assess the protective properties of the recombinant adenovirus. The level of viral shedding from the lungs of the infected mice was evaluated by titration of the lung homogenates in MDCK cell culture on days 3 and 6 after infection. The level of specific antibodies to H7 avian influenza virus was determined by indirect enzyme immunoassay. Results: the use of Ad5-tet-M2NP adenovirus for immunisation of the mice ensured 100% survival of the animals that had disease symptoms (weight loss) after their infection with the lethal dose (5 LD50) of H7 avian influenza virus. The study demonstrated a high post-vaccination level of humoral immune response to H7 avian influenza virus. The virus titer decreased significantly by day 6 in the lungs of mice that had been immunised with Ad5-tet-M2NP compared to the control group. Conclusion: the Ad5-tetM2NP recombinant adenovirus can be used to create a candidate pandemic influenza vaccine that would protect against avian influenza viruses, subtype H7, in particular
ΠΡΡΠ°ΡΠΈΠΈ Π² Π³Π΅Π½ΠΎΠΌΠ΅ Π²ΠΈΡΡΡΠΎΠ² Π³ΡΠΈΠΏΠΏΠ° ΠΏΡΠΈΡ ΠΏΠΎΠ΄ΡΠΈΠΏΠΎΠ² Π1 ΠΈ Π5, ΠΎΡΠ²Π΅ΡΡΡΠ²Π΅Π½Π½ΡΠ΅ Π·Π° Π°Π΄Π°ΠΏΡΠ°ΡΠΈΡ ΠΊ ΠΌΠ»Π΅ΠΊΠΎΠΏΠΈΡΠ°ΡΡΠΈΠΌ
Avian influenza viruses of H1 and H5 subtypes were involved in the formation of highly pathogenic viruses that caused pandemics and panzootics in the 20thβ21st centuries. In order to assess the zoonotic potential of viruses of these subtypes, two viruses of H1N1 and H5N3 have been isolated from wild ducks in Moscow and adapted to growth in mouse lungs. Their phenotypic properties were studied, and the genetic changes that occurred during adaptation were identified. The original A/duck/Moscow/4970/2013 (H1N1) and A/duck/Moscow/4182-C/2010 (H5N3) viruses were apathogenic for mice but became pathogenic after 7β10 passages in mouse lungs. Complete genome sequencing revealed 2 amino acid substitutions in the proteins of the H1N1 mouse-adapted variant (Glu627Lys in PB2 and Asp35Asn in hemagglutinin (HA) β numbering according to H3) and 6 mutations in the proteins of H5N3 virus (Glu627lys in PB2, Val113Ala in PB1, Ser82Pro in PB1-F2, Lys52Arg in HA2, Arg65Lys in NP, and Ser59Ile in NA). The increase in virulence is most likely due to a common substitution in the protein PB2 Glu627Lys as revealed in both viruses. The replacement of Asp35Asn in HA of the mouse-adapted H1N1 virus is associated with an increase in the pH value of the HA transition from 5.0 for 5.5 in comparison to the HA of parent virus. The found mutations in HA, NA, and PB1-F2 proteins of the adapted H5N3 variant are unique. The mutations Glu627Lys in PB2, Arg65Lys in NP, and Val113Ala in PB1 are most likely host adaptive.ΠΠΈΡΡΡΡ Π³ΡΠΈΠΏΠΏΠ° ΠΏΡΠΈΡ ΠΏΠΎΠ΄ΡΠΈΠΏΠΎΠ² Π1 ΠΈ Π5 ΡΡΠ°ΡΡΠ²ΠΎΠ²Π°Π»ΠΈ Π² ΡΠΎΡΠΌΠΈΡΠΎΠ²Π°Π½ΠΈΠΈ Π²ΡΡΠΎΠΊΠΎΠΏΠ°ΡΠΎΠ³Π΅Π½Π½ΡΡ
Π²Π°ΡΠΈΠ°Π½ΡΠΎΠ² Π²ΠΈΡΡΡΠΎΠ², Π²ΡΠ·Π²Π°Π²ΡΠΈΡ
ΠΏΠ°Π½Π΄Π΅ΠΌΠΈΠΈ ΠΈ Β ΠΏΠ°Π½Π·ΠΎΠΎΡΠΈΠΈ Π² Β XXβXXI Β Π²Π΅ΠΊΠ°Ρ
. Π‘ Β ΡΠ΅Π»ΡΡ ΠΎΡΠ΅Π½ΠΊΠΈ Π·ΠΎΠΎΠ½ΠΎΠ·Π½ΠΎΠ³ΠΎ ΠΏΠΎΡΠ΅Π½ΡΠΈΠ°Π»Π° Π²ΠΈΡΡΡΠΎΠ² ΡΡΠΈΡ
ΠΏΠΎΠ΄ΡΠΈΠΏΠΎΠ², Π²ΡΠ΄Π΅Π»Π΅Π½Π½ΡΡ
ΠΎΡ Π΄ΠΈΠΊΠΈΡ
ΡΡΠΎΠΊ Π² ΡΠ΅ΡΡΠ΅ ΠΠΎΡΠΊΠ²Ρ, Π±ΡΠ»Π° ΠΏΡΠΎΠ²Π΅Π΄Π΅Π½Π° Π°Π΄Π°ΠΏΡΠ°ΡΠΈΡ Π²ΠΈΡΡΡΠΎΠ² ΠΊ ΡΠ°Π·ΠΌΠ½ΠΎΠΆΠ΅Π½ΠΈΡ Π² Π»Π΅Π³ΠΊΠΈΡ
ΠΌΡΡΠ΅ΠΉ, ΠΈΠ·ΡΡΠ΅Π½Ρ ΠΈΡ
ΡΠ΅Π½ΠΎΡΠΈΠΏΠΈΡΠ΅ΡΠΊΠΈΠ΅ ΡΠ²ΠΎΠΉΡΡΠ²Π° ΠΈ ΠΈΠ΄Π΅Π½ΡΠΈΡΠΈΡΠΈΡΠΎΠ²Π°Π½Ρ Π³Π΅Π½Π΅ΡΠΈΡΠ΅ΡΠΊΠΈΠ΅ ΠΈΠ·ΠΌΠ΅Π½Π΅Π½ΠΈΡ, Π²ΠΎΠ·Π½ΠΈΠΊΡΠΈΠ΅ ΠΏΡΠΈ Π°Π΄Π°ΠΏΡΠ°ΡΠΈΠΈ. ΠΠ·Π½Π°ΡΠ°Π»ΡΠ½ΠΎ Π°ΠΏΠ°ΡΠΎΠ³Π΅Π½Π½ΡΠ΅ Π΄Π»Ρ ΠΌΡΡΠ΅ΠΉ Π²ΠΈΡΡΡΡ A/duck/Moscow/4970/2013 (H1N1) ΠΈ A/duck/Moscow/4182βC/2010 (H5N3) ΠΏΠΎΡΠ»Π΅ 7β10 ΠΏΠ°ΡΡΠ°ΠΆΠ΅ΠΉ ΡΠ΅ΡΠ΅Π· Π»Π΅Π³ΠΊΠΈΠ΅ ΠΌΡΡΠ΅ΠΉ ΠΈΠ·ΠΌΠ΅Π½ΠΈΠ»ΠΈ ΡΠ΅Π½ΠΎΡΠΈΠΏ Π½Π° ΠΏΠ°ΡΠΎΠ³Π΅Π½Π½ΡΠΉ. ΠΠΎΠ»Π½ΠΎΠ³Π΅Π½ΠΎΠΌΠ½ΠΎΠ΅ ΡΠ΅ΠΊΠ²Π΅Π½ΠΈΡΠΎΠ²Π°Π½ΠΈΠ΅ Π²ΡΡΠ²ΠΈΠ»ΠΎ Π² Π°Π΄Π°ΠΏΡΠΈΡΠΎΠ²Π°Π½Π½ΡΡ
ΠΊ ΠΌΡΡΠ°ΠΌ Π²ΠΈΡΡΡΠ°Ρ
2 Π°ΠΌΠΈΠ½ΠΎΠΊΠΈΡΠ»ΠΎΡΠ½ΡΠ΅ Π·Π°ΠΌΠ΅Π½Ρ Π² Π²ΠΈΡΡΡΠ΅ Π³ΡΠΈΠΏΠΏΠ° H1N1 (Glu627Lys Π² Π±Π΅Π»ΠΊΠ΅ PB2 ΠΈ Asp35Asn Π² Π³Π΅ΠΌΠ°Π³Π³Π»ΡΡΠΈΠ½ΠΈΠ½Π΅ (HA) β Π½ΡΠΌΠ΅ΡΠ°ΡΠΈΡ ΠΏΠΎ H3) ΠΈ 6 ΠΌΡΡΠ°ΡΠΈΠΉ Π² Π±Π΅Π»ΠΊΠ°Ρ
Π²ΠΈΡΡΡΠ° H5N3 (Glu627Lys Π² PB2, Val113Ala Π² PB1, Ser82Pro Π² PB1βF2, Lys52Arg Π² HA2, Arg65Lys Π² NP ΠΈ Ser59Ile Π² NA). ΠΠΎΠ·ΡΠ°ΡΡΠ°Π½ΠΈΠ΅ Π²ΠΈΡΡΠ»Π΅Π½ΡΠ½ΠΎΡΡΠΈ Π΄Π»Ρ ΠΌΡΡΠ΅ΠΉ, ΡΠΊΠΎΡΠ΅Π΅ Π²ΡΠ΅Π³ΠΎ, ΠΎΠ±ΡΡΠ»ΠΎΠ²Π»Π΅Π½ΠΎ ΠΎΠ±ΡΠ΅ΠΉ Π΄Π»Ρ ΠΎΠ±ΠΎΠΈΡ
Π²ΠΈΡΡΡΠΎΠ² Π·Π°ΠΌΠ΅Π½ΠΎΠΉ β Glu627Lys Π² Β Π±Π΅Π»ΠΊΠ΅ PB2. ΠΠ°ΠΌΠ΅Π½Π° Asp35Asn Π² Β HA Π°Π΄Π°ΠΏΡΠΈΡΠΎΠ²Π°Π½Π½ΠΎΠ³ΠΎ ΠΊ Β ΠΌΡΡΠ°ΠΌ Π²ΠΈΡΡΡΠ° Π³ΡΠΈΠΏΠΏΠ° H1N1 Β Π°ΡΡΠΎΡΠΈΠΈΡΠΎΠ²Π°Π½Π° Ρ Π²ΠΎΠ·ΡΠ°ΡΡΠ°Π½ΠΈΠ΅ΠΌ Π·Π½Π°ΡΠ΅Π½ΠΈΡ ΡΠ ΠΊΠΎΠ½ΡΠΎΡΠΌΠ°ΡΠΈΠΎΠ½Π½ΠΎΠ³ΠΎ ΠΏΠ΅ΡΠ΅Ρ
ΠΎΠ΄Π° HA Ρ 5.0 Π΄ΠΎ 5.5 ΠΎΡΠ½ΠΎΡΠΈΡΠ΅Π»ΡΠ½ΠΎ HA Π΄ΠΈΠΊΠΎΠ³ΠΎ Π²ΠΈΡΡΡΠ°. ΠΠ±Π½Π°ΡΡΠΆΠ΅Π½Π½ΡΠ΅ Π² Π°Π΄Π°ΠΏΡΠΈΡΠΎΠ²Π°Π½Π½ΠΎΠΌ Π²Π°ΡΠΈΠ°Π½ΡΠ΅ H5N3 ΠΌΡΡΠ°ΡΠΈΠΈ Π² Π±Π΅Π»ΠΊΠ°Ρ
ΠΠ, NA ΠΈ PB1βF2 β ΡΠ½ΠΈΠΊΠ°Π»ΡΠ½ΡΠ΅. ΠΡΡΠ°ΡΠΈΠΈ Glu627Lys Π² PB2, Arg65Lys Π² NP ΠΈ Val113Ala Π² PB1, ΡΠΊΠΎΡΠ΅Π΅ Π²ΡΠ΅Π³ΠΎ, Π½ΠΎΡΡΡ Π°Π΄Π°ΠΏΡΠ°ΡΠΈΠΎΠ½Π½ΡΠΉ Ρ
Π°ΡΠ°ΠΊΡΠ΅Ρ
ΠΠ°ΡΠΈΡΠ° ΠΌΡΡΠ΅ΠΉ ΠΎΡ Π·Π°ΡΠ°ΠΆΠ΅Π½ΠΈΡ Π²ΠΈΡΡΡΠΎΠΌ Π³ΡΠΈΠΏΠΏΠ° ΠΏΡΠΈΡ ΡΡΠ±ΡΠΈΠΏΠ° H7 Ρ ΠΏΠΎΠΌΠΎΡΡΡ ΠΈΠΌΠΌΡΠ½ΠΈΠ·Π°ΡΠΈΠΈ ΡΠ΅ΠΊΠΎΠΌΠ±ΠΈΠ½Π°Π½ΡΠ½ΡΠΌ Π°Π΄Π΅Π½ΠΎΠ²ΠΈΡΡΡΠΎΠΌ, ΠΊΠΎΠ΄ΠΈΡΡΡΡΠΈΠΌ ΠΊΠΎΠ½ΡΠ΅ΡΠ²Π°ΡΠΈΠ²Π½ΡΠ΅ Π°Π½ΡΠΈΠ³Π΅Π½Ρ Π²ΠΈΡΡΡΠ° Π³ΡΠΈΠΏΠΏΠ° Π
Influenza is a highly contagious disease that causes annual epidemics and occasional pandemics. Birds are believed to be the source of newly emerging pandemic strains, including highly pathogenic avian influenza viruses of the subtype H7. The aim of the study: to evaluate the ability of the recombinant human adenovirus, serotype 5, which expresses genes of influenza A highly conserved antigens (ion channel M2 and nucleoprotein NP), to provide protection to laboratory mice against infection with a lethal dose of avian influenza virus, subtype H7. To achieve this goal, it was necessary to adapt influenza A virus, subtype H7 for reproduction in the lungs of mice, to characterise it, and to use it for evaluation of the protective properties of the recombinant adenovirus. Materials and methods: avian influenza virus A/Chicken/NJ/294508-12/2004 (H7N2) was adapted for reproduction in the lungs of mice by repeated passages. The adapted strain was sequenced and assessed using hemagglutination test, EID50 and LD50 for laboratory mice. BALB/c mice were immunised once with Ad5-tet-M2NP adenovirus intranasally, and 21 days after the immunisation they were infected with a lethal dose (5 LD50) of influenza virus A/Chicken/NJ/294508-12/2004 (H7N2) in order to assess the protective properties of the recombinant adenovirus. The level of viral shedding from the lungs of the infected mice was evaluated by titration of the lung homogenates in MDCK cell culture on days 3 and 6 after infection. The level of specific antibodies to H7 avian influenza virus was determined by indirect enzyme immunoassay. Results: the use of Ad5-tet-M2NP adenovirus for immunisation of the mice ensured 100% survival of the animals that had disease symptoms (weight loss) after their infection with the lethal dose (5 LD50) of H7 avian influenza virus. The study demonstrated a high post-vaccination level of humoral immune response to H7 avian influenza virus. The virus titer decreased significantly by day 6 in the lungs of mice that had been immunised with Ad5-tet-M2NP compared to the control group. Conclusion: the Ad5-tetM2NP recombinant adenovirus can be used to create a candidate pandemic influenza vaccine that would protect against avian influenza viruses, subtype H7, in particular.ΠΡΠΈΠΏΠΏ β Π²ΡΡΠΎΠΊΠΎΠΊΠΎΠ½ΡΠ°Π³ΠΈΠΎΠ·Π½ΠΎΠ΅ Π·Π°Π±ΠΎΠ»Π΅Π²Π°Π½ΠΈΠ΅, Π²ΡΠ·ΡΠ²Π°ΡΡΠ΅Π΅ Π΅ΠΆΠ΅Π³ΠΎΠ΄Π½ΡΠ΅ ΡΠΏΠΈΠ΄Π΅ΠΌΠΈΠΈ ΠΈ ΡΠ΅ΡΠ΅Π· Π½Π΅ΡΠ°Π²Π½ΡΠ΅ ΠΈΠ½ΡΠ΅ΡΠ²Π°Π»Ρ Π²ΡΠ΅ΠΌΠ΅Π½ΠΈ β ΠΏΠ°Π½Π΄Π΅ΠΌΠΈΠΈ. ΠΡΡΠΎΡΠ½ΠΈΠΊΠΎΠΌ Π²Π½ΠΎΠ²Ρ Π²ΠΎΠ·Π½ΠΈΠΊΠ°ΡΡΠΈΡ
ΠΏΠ°Π½Π΄Π΅ΠΌΠΈΡΠ½ΡΡ
ΡΡΠ°ΠΌΠΌΠΎΠ², ΠΊΠ°ΠΊ ΠΏΡΠ°Π²ΠΈΠ»ΠΎ, ΡΠ²Π»ΡΡΡΡΡ ΠΏΡΠΈΡΡ, Π° Π½Π°ΠΈΠ±ΠΎΠ»ΡΡΠ΅Π΅ Π±Π΅ΡΠΏΠΎΠΊΠΎΠΉΡΡΠ²ΠΎ Π² Π½Π°ΡΡΠΎΡΡΠ΅Π΅ Π²ΡΠ΅ΠΌΡ Π²ΡΠ·ΡΠ²Π°ΡΡ Π²ΡΡΠΎΠΊΠΎΠΏΠ°ΡΠΎΠ³Π΅Π½Π½ΡΠ΅ Π²ΠΈΡΡΡΡ Π³ΡΠΈΠΏΠΏΠ° ΠΏΡΠΈΡ ΡΡΠ±ΡΠΈΠΏΠ° H7. Π¦Π΅Π»Ρ ΡΠ°Π±ΠΎΡΡ: ΠΎΡΠ΅Π½ΠΈΡΡ ΡΠΏΠΎΡΠΎΠ±Π½ΠΎΡΡΡ ΡΠ΅ΠΊΠΎΠΌΠ±ΠΈΠ½Π°Π½ΡΠ½ΠΎΠ³ΠΎ Π°Π΄Π΅Π½ΠΎΠ²ΠΈΡΡΡΠ° ΡΠ΅Π»ΠΎΠ²Π΅ΠΊΠ° ΠΏΡΡΠΎΠ³ΠΎ ΡΠ΅ΡΠΎΡΠΈΠΏΠ°, ΡΠΊΡΠΏΡΠ΅ΡΡΠΈΡΡΡΡΠ΅Π³ΠΎ Π³Π΅Π½Ρ Π²ΡΡΠΎΠΊΠΎΠΊΠΎΠ½ΡΠ΅ΡΠ²Π°ΡΠΈΠ²Π½ΡΡ
Π°Π½ΡΠΈΠ³Π΅Π½ΠΎΠ² Π²ΠΈΡΡΡΠ° Π³ΡΠΈΠΏΠΏΠ° Π (ΠΈΠΎΠ½Π½ΠΎΠ³ΠΎ ΠΊΠ°Π½Π°Π»Π° Π2 ΠΈ Π½ΡΠΊΠ»Π΅ΠΎΠΏΡΠΎΡΠ΅ΠΈΠ½Π° NP), ΠΎΠ±Π΅ΡΠΏΠ΅ΡΠΈΠ²Π°ΡΡ Π·Π°ΡΠΈΡΡ ΠΎΡ Π·Π°ΡΠ°ΠΆΠ΅Π½ΠΈΡ Π»Π°Π±ΠΎΡΠ°ΡΠΎΡΠ½ΡΡ
ΠΌΡΡΠ΅ΠΉ Π»Π΅ΡΠ°Π»ΡΠ½ΠΎΠΉ Π΄ΠΎΠ·ΠΎΠΉ Π²ΠΈΡΡΡΠ° Π³ΡΠΈΠΏΠΏΠ° ΠΏΡΠΈΡ ΡΡΠ±ΡΠΈΠΏΠ° H7. ΠΠ»Ρ Π΄ΠΎΡΡΠΈΠΆΠ΅Π½ΠΈΡ ΡΠ΅Π»ΠΈ Π½Π΅ΠΎΠ±Ρ
ΠΎΠ΄ΠΈΠΌΠΎ Π±ΡΠ»ΠΎ Π°Π΄Π°ΠΏΡΠΈΡΠΎΠ²Π°ΡΡ Π΄Π»Ρ ΡΠ°Π·ΠΌΠ½ΠΎΠΆΠ΅Π½ΠΈΡ Π² Π»Π΅Π³ΠΊΠΈΡ
ΠΌΡΡΠ΅ΠΉ Π²ΠΈΡΡΡ Π³ΡΠΈΠΏΠΏΠ° Π ΡΡΠ±ΡΠΈΠΏΠ° Π7, ΠΎΡ
Π°ΡΠ°ΠΊΡΠ΅ΡΠΈΠ·ΠΎΠ²Π°ΡΡ ΠΈ Ρ Π΅Π³ΠΎ ΠΏΠΎΠΌΠΎΡΡΡ ΠΎΡΠ΅Π½ΠΈΡΡ Π·Π°ΡΠΈΡΠ½ΡΠ΅ ΡΠ²ΠΎΠΉΡΡΠ²Π° ΡΠ΅ΠΊΠΎΠΌΠ±ΠΈΠ½Π°Π½ΡΠ½ΠΎΠ³ΠΎ Π°Π΄Π΅Π½ΠΎΠ²ΠΈΡΡΡΠ°. ΠΠ°ΡΠ΅ΡΠΈΠ°Π»Ρ ΠΈ ΠΌΠ΅ΡΠΎΠ΄Ρ: Π²ΠΈΡΡΡ Π³ΡΠΈΠΏΠΏΠ° ΠΏΡΠΈΡ A/Chicken/NJ/294508-12/2004 (H7N2) Π±ΡΠ» Π°Π΄Π°ΠΏΡΠΈΡΠΎΠ²Π°Π½ Π΄Π»Ρ ΡΠ°Π·ΠΌΠ½ΠΎΠΆΠ΅Π½ΠΈΡ Π² Π»Π΅Π³ΠΊΠΈΡ
ΠΌΡΡΠ΅ΠΉ ΠΏΡΡΠ΅ΠΌ ΠΌΠ½ΠΎΠ³ΠΎΠΊΡΠ°ΡΠ½ΠΎΠ³ΠΎ ΠΏΠ°ΡΡΠΈΡΠΎΠ²Π°Π½ΠΈΡ. ΠΡΠΎΡ ΡΡΠ°ΠΌΠΌ Π±ΡΠ» ΡΠ΅ΠΊΠ²Π΅Π½ΠΈΡΠΎΠ²Π°Π½ ΠΈ ΠΎΡ
Π°ΡΠ°ΠΊΡΠ΅ΡΠΈΠ·ΠΎΠ²Π°Π½ Π² ΡΠ΅Π°ΠΊΡΠΈΠΈ Π³Π΅ΠΌΠ°Π³Π³Π»ΡΡΠΈΠ½Π°ΡΠΈΠΈ, ΡΡΡΠ°Π½ΠΎΠ²Π»Π΅Π½Ρ Π΅Π³ΠΎ ΠΠΠ50 ΠΈ ΠΠ50 Π΄Π»Ρ Π»Π°Π±ΠΎΡΠ°ΡΠΎΡΠ½ΡΡ
ΠΌΡΡΠ΅ΠΉ. ΠΠ»Ρ ΠΈΠ·ΡΡΠ΅Π½ΠΈΡ Π·Π°ΡΠΈΡΠ½ΡΡ
ΡΠ²ΠΎΠΉΡΡΠ² ΡΠ΅ΠΊΠΎΠΌΠ±ΠΈΠ½Π°Π½ΡΠ½ΠΎΠ³ΠΎ Π°Π΄Π΅Π½ΠΎΠ²ΠΈΡΡΡΠ° ΠΌΡΡΠΈ Π»ΠΈΠ½ΠΈΠΈ BALB/c Π±ΡΠ»ΠΈ ΠΈΠΌΠΌΡΠ½ΠΈΠ·ΠΈΡΠΎΠ²Π°Π½Ρ Π°Π΄Π΅Π½ΠΎΠ²ΠΈΡΡΡΠΎΠΌ Ad5-tet-M2NP ΠΎΠ΄Π½ΠΎΠΊΡΠ°ΡΠ½ΠΎ ΠΈΠ½ΡΡΠ°Π½Π°Π·Π°Π»ΡΠ½ΠΎ ΠΈ ΡΠ΅ΡΠ΅Π· 21 ΡΡΡΠΊΠΈ ΠΏΠΎΡΠ»Π΅ ΠΈΠΌΠΌΡΠ½ΠΈΠ·Π°ΡΠΈΠΈ Π·Π°ΡΠ°ΠΆΠ΅Π½Ρ Π»Π΅ΡΠ°Π»ΡΠ½ΠΎΠΉ Π΄ΠΎΠ·ΠΎΠΉ (5 ΠΠ50) Π²ΠΈΡΡΡΠ° Π³ΡΠΈΠΏΠΏΠ° ΠΏΡΠΈΡ A/Chicken/NJ/294508-12/2004 (H7N2). Π£ΡΠΎΠ²Π΅Π½Ρ Π²ΠΈΡΡΡΠΎΠ²ΡΠ΄Π΅Π»Π΅Π½ΠΈΡ ΠΈΠ· Π»Π΅Π³ΠΊΠΈΡ
ΠΌΡΡΠ΅ΠΉ Π±ΡΠ» ΠΎΡΠ΅Π½Π΅Π½ Π½Π° 3 ΠΈ 6 ΡΡΡΠΊΠΈ ΠΏΠΎΡΠ»Π΅ Π·Π°ΡΠ°ΠΆΠ΅Π½ΠΈΡ Ρ ΠΏΠΎΠΌΠΎΡΡΡ ΡΠΈΡΡΠΎΠ²Π°Π½ΠΈΡ Π³ΠΎΠΌΠΎΠ³Π΅Π½Π°ΡΠΎΠ² Π»Π΅Π³ΠΊΠΈΡ
Π½Π° ΠΊΡΠ»ΡΡΡΡΠ΅ ΠΊΠ»Π΅ΡΠΎΠΊ MDCK. Π£ΡΠΎΠ²Π΅Π½Ρ ΡΠΏΠ΅ΡΠΈΡΠΈΡΠ΅ΡΠΊΠΈΡ
Π°Π½ΡΠΈΡΠ΅Π» ΠΊ Π²ΠΈΡΡΡΡ Π³ΡΠΈΠΏΠΏΠ° ΠΏΡΠΈΡ ΡΡΠ±ΡΠΈΠΏΠ° Π7 ΠΎΠΏΡΠ΅Π΄Π΅Π»ΡΠ»ΠΈ ΠΌΠ΅ΡΠΎΠ΄ΠΎΠΌ Π½Π΅ΠΏΡΡΠΌΠΎΠ³ΠΎ ΠΈΠΌΠΌΡΠ½ΠΎΡΠ΅ΡΠΌΠ΅Π½ΡΠ½ΠΎΠ³ΠΎ Π°Π½Π°Π»ΠΈΠ·Π°. Π Π΅Π·ΡΠ»ΡΡΠ°ΡΡ: ΠΈΠΌΠΌΡΠ½ΠΈΠ·Π°ΡΠΈΡ ΠΌΡΡΠ΅ΠΉ Π°Π΄Π΅Π½ΠΎΠ²ΠΈΡΡΡΠΎΠΌ Ad5-tet-M2NP ΠΏΡΠΈ Π½Π°Π»ΠΈΡΠΈΠΈ ΡΠΈΠΌΠΏΡΠΎΠΌΠΎΠ² Π·Π°Π±ΠΎΠ»Π΅Π²Π°Π½ΠΈΡ (ΡΠ½ΠΈΠΆΠ΅Π½ΠΈΠ΅ ΠΌΠ°ΡΡΡ ΡΠ΅Π»Π°) ΠΎΠ±Π΅ΡΠΏΠ΅ΡΠΈΠ»Π° 100% Π²ΡΠΆΠΈΠ²Π°Π΅ΠΌΠΎΡΡΡ ΠΆΠΈΠ²ΠΎΡΠ½ΡΡ
ΠΏΠΎΡΠ»Π΅ Π·Π°ΡΠ°ΠΆΠ΅Π½ΠΈΡ Π»Π΅ΡΠ°Π»ΡΠ½ΠΎΠΉ Π΄ΠΎΠ·ΠΎΠΉ (5 ΠΠ50) Π²ΠΈΡΡΡΠ° Π³ΡΠΈΠΏΠΏΠ° ΠΏΡΠΈΡ ΡΡΠ±ΡΠΈΠΏΠ° H7. ΠΡΠΎΠ΄Π΅ΠΌΠΎΠ½ΡΡΡΠΈΡΠΎΠ²Π°Π½ Π²ΡΡΠΎΠΊΠΈΠΉ ΠΏΠΎΡΡΠ²Π°ΠΊΡΠΈΠ½Π°Π»ΡΠ½ΡΠΉ ΡΡΠΎΠ²Π΅Π½Ρ Π³ΡΠΌΠΎΡΠ°Π»ΡΠ½ΠΎΠ³ΠΎ ΠΈΠΌΠΌΡΠ½Π½ΠΎΠ³ΠΎ ΠΎΡΠ²Π΅ΡΠ° ΠΊ Π²ΠΈΡΡΡΡ Π³ΡΠΈΠΏΠΏΠ° ΠΏΡΠΈΡ ΡΡΠ±ΡΠΈΠΏΠ° H7. ΠΠΎΠΊΠ°Π·Π°Π½ΠΎ, ΡΡΠΎ Π² Π»Π΅Π³ΠΊΠΈΡ
ΠΌΡΡΠ΅ΠΉ ΠΈΠ· Π³ΡΡΠΏΠΏΡ, ΠΈΠΌΠΌΡΠ½ΠΈΠ·ΠΈΡΠΎΠ²Π°Π½Π½ΠΎΠΉ Ad5-tet-M2NP, ΡΠΆΠ΅ ΠΊ 6 ΡΡΡΠΊΠ°ΠΌ Π½Π°Π±Π»ΡΠ΄Π°Π»ΠΎΡΡ ΡΡΡΠ΅ΡΡΠ²Π΅Π½Π½ΠΎΠ΅ ΡΠ½ΠΈΠΆΠ΅Π½ΠΈΠ΅ ΡΠΈΡΡΠ° Π²ΠΈΡΡΡΠ° Π³ΡΠΈΠΏΠΏΠ° ΠΏΡΠΈΡ ΡΡΠ±ΡΠΈΠΏΠ° H7 ΠΏΠΎ ΡΡΠ°Π²Π½Π΅Π½ΠΈΡ Ρ ΠΊΠΎΠ½ΡΡΠΎΠ»ΡΠ½ΠΎΠΉ Π³ΡΡΠΏΠΏΠΎΠΉ. ΠΠ°ΠΊΠ»ΡΡΠ΅Π½ΠΈΠ΅: ΡΠ΅ΠΊΠΎΠΌΠ±ΠΈΠ½Π°Π½ΡΠ½ΡΠΉ Π°Π΄Π΅Π½ΠΎΠ²ΠΈΡΡΡ Ad5-tet-M2NP ΠΌΠΎΠΆΠ΅Ρ Π±ΡΡΡ ΠΈΡΠΏΠΎΠ»ΡΠ·ΠΎΠ²Π°Π½ Π΄Π»Ρ ΡΠΎΠ·Π΄Π°Π½ΠΈΡ ΠΏΠΎΡΠ΅Π½ΡΠΈΠ°Π»ΡΠ½ΠΎΠΉ ΠΏΠ°Π½Π΄Π΅ΠΌΠΈΡΠ½ΠΎΠΉ ΠΏΡΠΎΡΠΈΠ²ΠΎΠ³ΡΠΈΠΏΠΏΠΎΠ·Π½ΠΎΠΉ Π²Π°ΠΊΡΠΈΠ½Ρ, Π² ΡΠΎΠΌ ΡΠΈΡΠ»Π΅ ΠΈ ΠΎΡ Π²ΠΈΡΡΡΠΎΠ² Π³ΡΠΈΠΏΠΏΠ° ΠΏΡΠΈΡ ΡΡΠ±ΡΠΈΠΏΠ°Β H7
The Features of The Hyperbolic Slab Waveguide
The dispersion relation determining guided TE and TM modes are found for the slab hyperbolic waveguide. The waveguide is consisting of an isotropic dielectric slab bounded by hyperbolic media. Some differences between the features of the waveguide under consideration and conventional ones are obtained. In particular, in the case of hyperbolic waveguide TM modes have two cutoff frequencies. As a result the number of modes is limited. Both TE and TM modes have nonzero cutoff frequencies, even though waveguide is symmetric one. For the TE and TM modes the Poynting vector component along the waveβs propagation axis could be equal to zero
The Features of The Hyperbolic Slab Waveguide
The dispersion relation determining guided TE and TM modes are found for the slab hyperbolic waveguide. The waveguide is consisting of an isotropic dielectric slab bounded by hyperbolic media. Some differences between the features of the waveguide under consideration and conventional ones are obtained. In particular, in the case of hyperbolic waveguide TM modes have two cutoff frequencies. As a result the number of modes is limited. Both TE and TM modes have nonzero cutoff frequencies, even though waveguide is symmetric one. For the TE and TM modes the Poynting vector component along the waveβs propagation axis could be equal to zero