43 research outputs found

    Practices of Protest in the Conditions of the Developing Academic Capitalism

    Get PDF
    The article focuses on the problem of professional motivation of University teaching staff in the context of developing β€œacademic capitalism” and presents the results of the empirical study carried out by the authors at the North-Western Institute of management of RANEPA in March–June 2020. Based on the data obtained, it is revealed that teachers, experiencing deep deprivation of their social needs – 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 – 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

    Get PDF
    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

    ΠœΡƒΡ‚Π°Ρ†ΠΈΠΈ Π² Π³Π΅Π½ΠΎΠΌΠ΅ вирусов Π³Ρ€ΠΈΠΏΠΏΠ° ΠΏΡ‚ΠΈΡ† ΠΏΠΎΠ΄Ρ‚ΠΈΠΏΠΎΠ² Н1 ΠΈ Н5, отвСтствСнныС Π·Π° Π°Π΄Π°ΠΏΡ‚Π°Ρ†ΠΈΡŽ ΠΊ ΠΌΠ»Π΅ΠΊΠΎΠΏΠΈΡ‚Π°ΡŽΡ‰ΠΈΠΌ

    Get PDF
    Avian influenza viruses of H1 and H5 subtypes were involved in the formation of highly pathogenic viruses that caused pandemics and panzootics in the 20th–21st 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 7–10 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) – 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.Вирусы Π³Ρ€ΠΈΠΏΠΏΠ° ΠΏΡ‚ΠΈΡ† ΠΏΠΎΠ΄Ρ‚ΠΈΠΏΠΎΠ² Н1 ΠΈ Н5 участвовали Π² Ρ„ΠΎΡ€ΠΌΠΈΡ€ΠΎΠ²Π°Π½ΠΈΠΈ высокопатогСнных Π²Π°Ρ€ΠΈΠ°Π½Ρ‚ΠΎΠ² вирусов, Π²Ρ‹Π·Π²Π°Π²ΡˆΠΈΡ… ΠΏΠ°Π½Π΄Π΅ΠΌΠΈΠΈ ΠΈ Β ΠΏΠ°Π½Π·ΠΎΠΎΡ‚ΠΈΠΈ Π² Β XX–XXI Β Π²Π΅ΠΊΠ°Ρ…. Π‘ Β Ρ†Π΅Π»ΡŒΡŽ ΠΎΡ†Π΅Π½ΠΊΠΈ Π·ΠΎΠΎΠ½ΠΎΠ·Π½ΠΎΠ³ΠΎ ΠΏΠΎΡ‚Π΅Π½Ρ†ΠΈΠ°Π»Π° вирусов этих ΠΏΠΎΠ΄Ρ‚ΠΈΠΏΠΎΠ², Π²Ρ‹Π΄Π΅Π»Π΅Π½Π½Ρ‹Ρ… ΠΎΡ‚ Π΄ΠΈΠΊΠΈΡ… ΡƒΡ‚ΠΎΠΊ Π² Ρ‡Π΅Ρ€Ρ‚Π΅ ΠœΠΎΡΠΊΠ²Ρ‹, Π±Ρ‹Π»Π° ΠΏΡ€ΠΎΠ²Π΅Π΄Π΅Π½Π° адаптация вирусов ΠΊ Ρ€Π°Π·ΠΌΠ½ΠΎΠΆΠ΅Π½ΠΈΡŽ Π² Π»Π΅Π³ΠΊΠΈΡ… ΠΌΡ‹ΡˆΠ΅ΠΉ, ΠΈΠ·ΡƒΡ‡Π΅Π½Ρ‹ ΠΈΡ… фСнотипичСскиС свойства ΠΈ ΠΈΠ΄Π΅Π½Ρ‚ΠΈΡ„ΠΈΡ†ΠΈΡ€ΠΎΠ²Π°Π½Ρ‹ гСнСтичСскиС измСнСния, возникшиС ΠΏΡ€ΠΈ Π°Π΄Π°ΠΏΡ‚Π°Ρ†ΠΈΠΈ. Π˜Π·Π½Π°Ρ‡Π°Π»ΡŒΠ½ΠΎ Π°ΠΏΠ°Ρ‚ΠΎΠ³Π΅Π½Π½Ρ‹Π΅ для ΠΌΡ‹ΡˆΠ΅ΠΉ вирусы A/duck/Moscow/4970/2013 (H1N1) ΠΈ A/duck/Moscow/4182‑C/2010 (H5N3) послС 7–10 пассаТСй Ρ‡Π΅Ρ€Π΅Π· Π»Π΅Π³ΠΊΠΈΠ΅ ΠΌΡ‹ΡˆΠ΅ΠΉ ΠΈΠ·ΠΌΠ΅Π½ΠΈΠ»ΠΈ Ρ„Π΅Π½ΠΎΡ‚ΠΈΠΏ Π½Π° ΠΏΠ°Ρ‚ΠΎΠ³Π΅Π½Π½Ρ‹ΠΉ. ПолногСномноС сСквСнированиС выявило Π² Π°Π΄Π°ΠΏΡ‚ΠΈΡ€ΠΎΠ²Π°Π½Π½Ρ‹Ρ… ΠΊ ΠΌΡ‹ΡˆΠ°ΠΌ вирусах 2 аминокислотныС Π·Π°ΠΌΠ΅Π½Ρ‹ Π² вирусС Π³Ρ€ΠΈΠΏΠΏΠ° H1N1 (Glu627Lys Π² Π±Π΅Π»ΠΊΠ΅ PB2 ΠΈ Asp35Asn Π² Π³Π΅ΠΌΠ°Π³Π³Π»ΡŽΡ‚ΠΈΠ½ΠΈΠ½Π΅ (HA) β€” нумСрация ΠΏΠΎ H3) ΠΈ 6 ΠΌΡƒΡ‚Π°Ρ†ΠΈΠΉ Π² Π±Π΅Π»ΠΊΠ°Ρ… вируса H5N3 (Glu627Lys Π² PB2, Val113Ala Π² PB1, Ser82Pro Π² PB1‑F2, Lys52Arg Π² HA2, Arg65Lys Π² NP ΠΈ Ser59Ile Π² NA). ВозрастаниС вирулСнтности для ΠΌΡ‹ΡˆΠ΅ΠΉ, скорСС всСго, обусловлСно ΠΎΠ±Ρ‰Π΅ΠΉ для ΠΎΠ±ΠΎΠΈΡ… вирусов Π·Π°ΠΌΠ΅Π½ΠΎΠΉ – Glu627Lys Π² Β Π±Π΅Π»ΠΊΠ΅ PB2. Π—Π°ΠΌΠ΅Π½Π° Asp35Asn Π² Β HA Π°Π΄Π°ΠΏΡ‚ΠΈΡ€ΠΎΠ²Π°Π½Π½ΠΎΠ³ΠΎ ΠΊ Β ΠΌΡ‹ΡˆΠ°ΠΌ вируса Π³Ρ€ΠΈΠΏΠΏΠ° H1N1  ассоциирована с возрастаниСм значСния рН ΠΊΠΎΠ½Ρ„ΠΎΡ€ΠΌΠ°Ρ†ΠΈΠΎΠ½Π½ΠΎΠ³ΠΎ ΠΏΠ΅Ρ€Π΅Ρ…ΠΎΠ΄Π° HA с 5.0 Π΄ΠΎ 5.5 ΠΎΡ‚Π½ΠΎΡΠΈΡ‚Π΅Π»ΡŒΠ½ΠΎ HA Π΄ΠΈΠΊΠΎΠ³ΠΎ вируса. ΠžΠ±Π½Π°Ρ€ΡƒΠΆΠ΅Π½Π½Ρ‹Π΅ Π² Π°Π΄Π°ΠΏΡ‚ΠΈΡ€ΠΎΠ²Π°Π½Π½ΠΎΠΌ Π²Π°Ρ€ΠΈΠ°Π½Ρ‚Π΅ H5N3 ΠΌΡƒΡ‚Π°Ρ†ΠΈΠΈ Π² Π±Π΅Π»ΠΊΠ°Ρ… НА, NA ΠΈ PB1‑F2 β€” ΡƒΠ½ΠΈΠΊΠ°Π»ΡŒΠ½Ρ‹Π΅. ΠœΡƒΡ‚Π°Ρ†ΠΈΠΈ Glu627Lys Π² PB2, Arg65Lys Π² NP ΠΈ Val113Ala Π² PB1, скорСС всСго, носят Π°Π΄Π°ΠΏΡ‚Π°Ρ†ΠΈΠΎΠ½Π½Ρ‹ΠΉ Ρ…Π°Ρ€Π°ΠΊΡ‚Π΅Ρ€

    Π—Π°Ρ‰ΠΈΡ‚Π° ΠΌΡ‹ΡˆΠ΅ΠΉ ΠΎΡ‚ зараТСния вирусом Π³Ρ€ΠΈΠΏΠΏΠ° ΠΏΡ‚ΠΈΡ† субтипа H7 с ΠΏΠΎΠΌΠΎΡ‰ΡŒΡŽ ΠΈΠΌΠΌΡƒΠ½ΠΈΠ·Π°Ρ†ΠΈΠΈ Ρ€Π΅ΠΊΠΎΠΌΠ±ΠΈΠ½Π°Π½Ρ‚Π½Ρ‹ΠΌ адСновирусом, ΠΊΠΎΠ΄ΠΈΡ€ΡƒΡŽΡ‰ΠΈΠΌ консСрвативныС Π°Π½Ρ‚ΠΈΠ³Π΅Π½Ρ‹ вируса Π³Ρ€ΠΈΠΏΠΏΠ° А

    Get PDF
    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.Π“Ρ€ΠΈΠΏΠΏ – высококонтагиозноС Π·Π°Π±ΠΎΠ»Π΅Π²Π°Π½ΠΈΠ΅, Π²Ρ‹Π·Ρ‹Π²Π°ΡŽΡ‰Π΅Π΅ Π΅ΠΆΠ΅Π³ΠΎΠ΄Π½Ρ‹Π΅ эпидСмии ΠΈ Ρ‡Π΅Ρ€Π΅Π· Π½Π΅Ρ€Π°Π²Π½Ρ‹Π΅ ΠΈΠ½Ρ‚Π΅Ρ€Π²Π°Π»Ρ‹ Π²Ρ€Π΅ΠΌΠ΅Π½ΠΈ – ΠΏΠ°Π½Π΄Π΅ΠΌΠΈΠΈ. Π˜ΡΡ‚ΠΎΡ‡Π½ΠΈΠΊΠΎΠΌ вновь Π²ΠΎΠ·Π½ΠΈΠΊΠ°ΡŽΡ‰ΠΈΡ… ΠΏΠ°Π½Π΄Π΅ΠΌΠΈΡ‡Π½Ρ‹Ρ… ΡˆΡ‚Π°ΠΌΠΌΠΎΠ², ΠΊΠ°ΠΊ ΠΏΡ€Π°Π²ΠΈΠ»ΠΎ, ΡΠ²Π»ΡΡŽΡ‚ΡΡ ΠΏΡ‚ΠΈΡ†Ρ‹, Π° наибольшСС бСспокойство Π² настоящСС врСмя Π²Ρ‹Π·Ρ‹Π²Π°ΡŽΡ‚ высокопатогСнныС вирусы Π³Ρ€ΠΈΠΏΠΏΠ° ΠΏΡ‚ΠΈΡ† субтипа H7. ЦСль Ρ€Π°Π±ΠΎΡ‚Ρ‹: ΠΎΡ†Π΅Π½ΠΈΡ‚ΡŒ ΡΠΏΠΎΡΠΎΠ±Π½ΠΎΡΡ‚ΡŒ Ρ€Π΅ΠΊΠΎΠΌΠ±ΠΈΠ½Π°Π½Ρ‚Π½ΠΎΠ³ΠΎ адСновируса Ρ‡Π΅Π»ΠΎΠ²Π΅ΠΊΠ° пятого сСротипа, ΡΠΊΡΠΏΡ€Π΅ΡΡΠΈΡ€ΡƒΡŽΡ‰Π΅Π³ΠΎ Π³Π΅Π½Ρ‹ высококонсСрвативных Π°Π½Ρ‚ΠΈΠ³Π΅Π½ΠΎΠ² вируса Π³Ρ€ΠΈΠΏΠΏΠ° А (ΠΈΠΎΠ½Π½ΠΎΠ³ΠΎ ΠΊΠ°Π½Π°Π»Π° М2 ΠΈ Π½ΡƒΠΊΠ»Π΅ΠΎΠΏΡ€ΠΎΡ‚Π΅ΠΈΠ½Π° NP), ΠΎΠ±Π΅ΡΠΏΠ΅Ρ‡ΠΈΠ²Π°Ρ‚ΡŒ Π·Π°Ρ‰ΠΈΡ‚Ρƒ ΠΎΡ‚ зараТСния Π»Π°Π±ΠΎΡ€Π°Ρ‚ΠΎΡ€Π½Ρ‹Ρ… ΠΌΡ‹ΡˆΠ΅ΠΉ Π»Π΅Ρ‚Π°Π»ΡŒΠ½ΠΎΠΉ Π΄ΠΎΠ·ΠΎΠΉ вируса Π³Ρ€ΠΈΠΏΠΏΠ° ΠΏΡ‚ΠΈΡ† субтипа H7. Для достиТСния Ρ†Π΅Π»ΠΈ Π½Π΅ΠΎΠ±Ρ…ΠΎΠ΄ΠΈΠΌΠΎ Π±Ρ‹Π»ΠΎ Π°Π΄Π°ΠΏΡ‚ΠΈΡ€ΠΎΠ²Π°Ρ‚ΡŒ для размноТСния Π² Π»Π΅Π³ΠΊΠΈΡ… ΠΌΡ‹ΡˆΠ΅ΠΉ вирус Π³Ρ€ΠΈΠΏΠΏΠ° А субтипа Н7, ΠΎΡ…Π°Ρ€Π°ΠΊΡ‚Π΅Ρ€ΠΈΠ·ΠΎΠ²Π°Ρ‚ΡŒ ΠΈ с Π΅Π³ΠΎ ΠΏΠΎΠΌΠΎΡ‰ΡŒΡŽ ΠΎΡ†Π΅Π½ΠΈΡ‚ΡŒ Π·Π°Ρ‰ΠΈΡ‚Π½Ρ‹Π΅ свойства Ρ€Π΅ΠΊΠΎΠΌΠ±ΠΈΠ½Π°Π½Ρ‚Π½ΠΎΠ³ΠΎ адСновируса. ΠœΠ°Ρ‚Π΅Ρ€ΠΈΠ°Π»Ρ‹ ΠΈ ΠΌΠ΅Ρ‚ΠΎΠ΄Ρ‹: вирус Π³Ρ€ΠΈΠΏΠΏΠ° ΠΏΡ‚ΠΈΡ† A/Chicken/NJ/294508-12/2004 (H7N2) Π±Ρ‹Π» Π°Π΄Π°ΠΏΡ‚ΠΈΡ€ΠΎΠ²Π°Π½ для размноТСния Π² Π»Π΅Π³ΠΊΠΈΡ… ΠΌΡ‹ΡˆΠ΅ΠΉ ΠΏΡƒΡ‚Π΅ΠΌ ΠΌΠ½ΠΎΠ³ΠΎΠΊΡ€Π°Ρ‚Π½ΠΎΠ³ΠΎ пассирования. Π­Ρ‚ΠΎΡ‚ ΡˆΡ‚Π°ΠΌΠΌ Π±Ρ‹Π» сСквСнирован ΠΈ ΠΎΡ…Π°Ρ€Π°ΠΊΡ‚Π΅Ρ€ΠΈΠ·ΠΎΠ²Π°Π½ Π² Ρ€Π΅Π°ΠΊΡ†ΠΈΠΈ Π³Π΅ΠΌΠ°Π³Π³Π»ΡŽΡ‚ΠΈΠ½Π°Ρ†ΠΈΠΈ, установлСны Π΅Π³ΠΎ Π­Π˜Π”50 ΠΈ Π›Π”50 для Π»Π°Π±ΠΎΡ€Π°Ρ‚ΠΎΡ€Π½Ρ‹Ρ… ΠΌΡ‹ΡˆΠ΅ΠΉ. Для изучСния Π·Π°Ρ‰ΠΈΡ‚Π½Ρ‹Ρ… свойств Ρ€Π΅ΠΊΠΎΠΌΠ±ΠΈΠ½Π°Π½Ρ‚Π½ΠΎΠ³ΠΎ адСновируса ΠΌΡ‹ΡˆΠΈ Π»ΠΈΠ½ΠΈΠΈ BALB/c Π±Ρ‹Π»ΠΈ ΠΈΠΌΠΌΡƒΠ½ΠΈΠ·ΠΈΡ€ΠΎΠ²Π°Π½Ρ‹ адСновирусом Ad5-tet-M2NP ΠΎΠ΄Π½ΠΎΠΊΡ€Π°Ρ‚Π½ΠΎ ΠΈΠ½Ρ‚Ρ€Π°Π½Π°Π·Π°Π»ΡŒΠ½ΠΎ ΠΈ Ρ‡Π΅Ρ€Π΅Π· 21 сутки послС ΠΈΠΌΠΌΡƒΠ½ΠΈΠ·Π°Ρ†ΠΈΠΈ Π·Π°Ρ€Π°ΠΆΠ΅Π½Ρ‹ Π»Π΅Ρ‚Π°Π»ΡŒΠ½ΠΎΠΉ Π΄ΠΎΠ·ΠΎΠΉ (5 Π›Π”50) вируса Π³Ρ€ΠΈΠΏΠΏΠ° ΠΏΡ‚ΠΈΡ† A/Chicken/NJ/294508-12/2004 (H7N2). Π£Ρ€ΠΎΠ²Π΅Π½ΡŒ вирусовыдСлСния ΠΈΠ· Π»Π΅Π³ΠΊΠΈΡ… ΠΌΡ‹ΡˆΠ΅ΠΉ Π±Ρ‹Π» ΠΎΡ†Π΅Π½Π΅Π½ Π½Π° 3 ΠΈ 6 сутки послС зараТСния с ΠΏΠΎΠΌΠΎΡ‰ΡŒΡŽ титрования Π³ΠΎΠΌΠΎΠ³Π΅Π½Π°Ρ‚ΠΎΠ² Π»Π΅Π³ΠΊΠΈΡ… Π½Π° ΠΊΡƒΠ»ΡŒΡ‚ΡƒΡ€Π΅ ΠΊΠ»Π΅Ρ‚ΠΎΠΊ MDCK. Π£Ρ€ΠΎΠ²Π΅Π½ΡŒ спСцифичСских Π°Π½Ρ‚ΠΈΡ‚Π΅Π» ΠΊ вирусу Π³Ρ€ΠΈΠΏΠΏΠ° ΠΏΡ‚ΠΈΡ† субтипа Н7 опрСдСляли ΠΌΠ΅Ρ‚ΠΎΠ΄ΠΎΠΌ нСпрямого ΠΈΠΌΠΌΡƒΠ½ΠΎΡ„Π΅Ρ€ΠΌΠ΅Π½Ρ‚Π½ΠΎΠ³ΠΎ Π°Π½Π°Π»ΠΈΠ·Π°. Π Π΅Π·ΡƒΠ»ΡŒΡ‚Π°Ρ‚Ρ‹: иммунизация ΠΌΡ‹ΡˆΠ΅ΠΉ адСновирусом Ad5-tet-M2NP ΠΏΡ€ΠΈ Π½Π°Π»ΠΈΡ‡ΠΈΠΈ симптомов заболСвания (сниТСниС массы Ρ‚Π΅Π»Π°) обСспСчила 100% Π²Ρ‹ΠΆΠΈΠ²Π°Π΅ΠΌΠΎΡΡ‚ΡŒ ΠΆΠΈΠ²ΠΎΡ‚Π½Ρ‹Ρ… послС зараТСния Π»Π΅Ρ‚Π°Π»ΡŒΠ½ΠΎΠΉ Π΄ΠΎΠ·ΠΎΠΉ (5 Π›Π”50) вируса Π³Ρ€ΠΈΠΏΠΏΠ° ΠΏΡ‚ΠΈΡ† субтипа H7. ΠŸΡ€ΠΎΠ΄Π΅ΠΌΠΎΠ½ΡΡ‚Ρ€ΠΈΡ€ΠΎΠ²Π°Π½ высокий ΠΏΠΎΡΡ‚Π²Π°ΠΊΡ†ΠΈΠ½Π°Π»ΡŒΠ½Ρ‹ΠΉ ΡƒΡ€ΠΎΠ²Π΅Π½ΡŒ Π³ΡƒΠΌΠΎΡ€Π°Π»ΡŒΠ½ΠΎΠ³ΠΎ ΠΈΠΌΠΌΡƒΠ½Π½ΠΎΠ³ΠΎ ΠΎΡ‚Π²Π΅Ρ‚Π° ΠΊ вирусу Π³Ρ€ΠΈΠΏΠΏΠ° ΠΏΡ‚ΠΈΡ† субтипа H7. Показано, Ρ‡Ρ‚ΠΎ Π² Π»Π΅Π³ΠΊΠΈΡ… ΠΌΡ‹ΡˆΠ΅ΠΉ ΠΈΠ· Π³Ρ€ΡƒΠΏΠΏΡ‹, ΠΈΠΌΠΌΡƒΠ½ΠΈΠ·ΠΈΡ€ΠΎΠ²Π°Π½Π½ΠΎΠΉ Ad5-tet-M2NP, ΡƒΠΆΠ΅ ΠΊ 6 суткам наблюдалось сущСствСнноС сниТСниС Ρ‚ΠΈΡ‚Ρ€Π° вируса Π³Ρ€ΠΈΠΏΠΏΠ° ΠΏΡ‚ΠΈΡ† субтипа H7 ΠΏΠΎ ΡΡ€Π°Π²Π½Π΅Π½ΠΈΡŽ с ΠΊΠΎΠ½Ρ‚Ρ€ΠΎΠ»ΡŒΠ½ΠΎΠΉ Π³Ρ€ΡƒΠΏΠΏΠΎΠΉ. Π—Π°ΠΊΠ»ΡŽΡ‡Π΅Π½ΠΈΠ΅: Ρ€Π΅ΠΊΠΎΠΌΠ±ΠΈΠ½Π°Π½Ρ‚Π½Ρ‹ΠΉ адСновирус Ad5-tet-M2NP ΠΌΠΎΠΆΠ΅Ρ‚ Π±Ρ‹Ρ‚ΡŒ использован для создания ΠΏΠΎΡ‚Π΅Π½Ρ†ΠΈΠ°Π»ΡŒΠ½ΠΎΠΉ ΠΏΠ°Π½Π΄Π΅ΠΌΠΈΡ‡Π½ΠΎΠΉ ΠΏΡ€ΠΎΡ‚ΠΈΠ²ΠΎΠ³Ρ€ΠΈΠΏΠΏΠΎΠ·Π½ΠΎΠΉ Π²Π°ΠΊΡ†ΠΈΠ½Ρ‹, Π² Ρ‚ΠΎΠΌ числС ΠΈ ΠΎΡ‚ вирусов Π³Ρ€ΠΈΠΏΠΏΠ° ΠΏΡ‚ΠΈΡ† субтипа H7

    Control problems for viscous stratified fluid

    No full text

    The Features of The Hyperbolic Slab Waveguide

    No full text
    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 wave’s propagation axis could be equal to zero

    The Features of The Hyperbolic Slab Waveguide

    No full text
    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 wave’s propagation axis could be equal to zero
    corecore