Cargando…

Advances in virus research Volume 111 /

Detalles Bibliográficos
Clasificación:Libro Electrónico
Otros Autores: Mettenleiter, Thomas C. (Editor ), Kielian, Margaret C., 1952- (Editor ), Roossinck, Marilyn J. (Editor )
Formato: Electrónico eBook
Idioma:Inglés
Publicado: Cambridge, MA : Academic Press, 2021.
Colección:Advances in virus research ; v. 111
Temas:
Acceso en línea:Texto completo

MARC

LEADER 00000cam a2200000Ii 4500
001 SCIDIR_on1280314757
003 OCoLC
005 20231120010611.0
006 m o d
007 cr cnu---unuuu
008 211025s2021 mau o 000 0 eng d
040 |a OPELS  |b eng  |e rda  |e pn  |c OPELS  |d OCLCF  |d OCLCO  |d SFB  |d OCLCQ  |d AAA  |d OCLCO 
020 |z 9780128246054 
020 |z 0128246057 
035 |a (OCoLC)1280314757 
050 4 |a QR360 
082 0 4 |a 579.2  |2 23 
245 0 0 |a Advances in virus research  |n Volume 111 /  |c edited by Thomas C. Mettenleiter, Margaret Kielian, Marilyn J. Roossinck. 
264 1 |a Cambridge, MA :  |b Academic Press,  |c 2021. 
300 |a 1 online resource (1 volume) 
336 |a text  |b txt  |2 rdacontent 
337 |a computer  |b c  |2 rdamedia 
338 |a online resource  |b cr  |2 rdacarrier 
490 0 |a Advances in virus research ;  |v v. 111 
588 0 |a Print version record. 
505 0 |a Intro -- Advances in Virus Research -- Copyright -- Contents -- Contributors -- Chapter One: Parainfluenza virus entry at the onset of infection -- 1. Introduction to parainfluenza virus infection and entry -- 2. HN�s structure and receptor binding -- 3. F: Primed for action in its pre-fusion state -- 4. HN interaction with F and HN�s role in the activation of F -- 5. The transient intermediate state of F -- 6. Final stages of fusion and entry -- 7. Fitness requirements of the HN/F fusion complex in human lung -- 8. Inhibitors of entry -- 8.1. Antivirals targeting HN�s role in receptor binding -- 8.2. Hijacking HN to trigger F prematurely -- 8.3. Antibodies that target F�s conformation or HN-F interaction -- 8.4. Blocking fusion at F�s transitional intermediate state -- 9. Future directions -- Acknowledgments -- References -- Chapter Two: Molecular archeology of human viruses -- 1. Three decades of aDNA research and more than a century of virology set expectations for archeovirology -- 1.1. Lessons from aDNA and aRNA -- 1.2. Lessons from virology -- 2. Promises and pitfalls of archeovirology -- 2.1. Survival, detectability and authentication of ancient viral sequences -- 2.1.1. Specimen/sample types -- 2.1.2. Selection/detection method -- 2.1.3. Authentication/phylogenetic dating criterion -- 2.2. Key questions of archeovirology -- 2.2.1. Origins and timescales -- 2.2.2. Diversity and its temporal dynamics -- 3. Outlook -- References -- Chapter Three: Advancing phage therapy through the lens of virus host-breadth and emergence potential -- 1. Phage biology, and the history and promise of phage therapy -- 1.1. Combating antibiotic-resistant bacteria could capitalize on lytic phage biology -- 1.2. Historical development of phage therapy -- 1.2.1. Discovery of phages -- 1.2.2. Politics of phage therapy -- 1.2.3. Phage therapy vs antibiotics. 
505 8 |a 1.3. Phage therapy offers many advantages over traditional antibiotics -- 1.4. Limitations to phage therapy -- 2. Phage host-range and development of generalized treatment -- 2.1. Host-range (specialism vs generalism) in lytic phages -- 2.2. Considerations for using few vs many phages in administered treatment -- 2.3. Observations and measures of host-range breadth in phages -- 2.4. Case example: Exploring host-range of lytic phages targeting P. aeruginosa -- 2.4.1. Study design to test killing ability of naturally-occurring phages across challenge hosts -- 2.4.2. Naturally-occurring phages differ in relative specialism vs generalism in host-use -- 2.4.3. Phage productivity on susceptible bacteria is additionally informative for gauging host-breadth -- 2.4.4. Using ``greedy algorithms�� to estimate useful combinations of phages for generalized treatment -- 2.4.5. Testing efficacy of a cocktail using in-vitro experiments on known and novel host strains -- 3. Phages can evolve in response to their environments, potentially altering host breadth -- 3.1. Evolution and ecology matter in phage-therapy development -- 3.1.1. Mutation rates affect phage evolution -- 3.1.2. Beyond mutations: Other sources of genetic material -- 3.1.3. Phages can evolve during treatment -- 3.1.4. Lessons from the emergence of zoonotic diseases -- 3.1.5. Lessons from experimental evolution -- 4. Conclusion -- Acknowledgments -- Appendix -- References -- Chapter Four: Alphavirus RNA replication in vertebrate cells -- 1. Introduction -- 2. Viral components of the RNA replication machinery -- 2.1. Precursors of ns-proteins -- 2.2. nsP1 -- 2.3. nsP2 -- 2.4. nsP3 -- 2.5. nsP4 -- 3. Host components of RNA replication machinery -- 4. Architecture, functioning, biogenesis and properties of replication complexes. 
505 8 |a 5. Functional interactions between components of alphavirus RNA replication machinery -- 6. Replicase inhibitors -- 7. Conclusions and perspectives -- Acknowledgments -- References. 
650 0 |a Virology. 
650 0 |a Virology  |x Research. 
650 6 |a Virologie.  |0 (CaQQLa)201-0008933 
650 6 |a Virologie  |x Recherche.  |0 (CaQQLa)201-0032557 
650 7 |a Virology  |2 fast  |0 (OCoLC)fst01167670 
650 7 |a Virology  |x Research  |2 fast  |0 (OCoLC)fst01167675 
700 1 |a Mettenleiter, Thomas C.,  |e editor. 
700 1 |a Kielian, Margaret C.,  |d 1952-  |e editor. 
700 1 |a Roossinck, Marilyn J.,  |e editor. 
776 0 8 |i Print version:  |t Advances in virus research. Volume 111.  |d Amsterdam : Academic Press, 2021  |z 9780128246054  |w (OCoLC)1272893343 
856 4 0 |u https://sciencedirect.uam.elogim.com/science/bookseries/00653527/111  |z Texto completo