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1 ty has highlighted the threat of a potential pandemic.
2 ght have changed, increasing the threat of a pandemic.
3 za virus emerged in humans, causing a global pandemic.
4 in, where HIV-1 expanded early in the global pandemic.
5 ong people and cause a devastating worldwide pandemic.
6 nza pandemics, as in the 2009 H1N1 influenza pandemic.
7 l strains decades after the emergence of the pandemic.
8 milar to that described during the 2009 H1N1 pandemic.
9 phibian declines driven by a global wildlife pandemic.
10 ght after in order to stem the current HIV-1 pandemic.
11 xplain the frequent failure of AIV to become pandemic.
12 f the regions involved in the current global pandemic.
13 w of opportunity for vaccination in a future pandemic.
14 ndicate a correlation with the spread of the pandemic.
15 orefront of health promotion to address this pandemic.
16 dity and mortality during the 2009 influenza pandemic.
17 limited by neglected populations and the HIV pandemic.
18 d from human to human and cause an influenza pandemic.
19 acterium tuberculosis, remains a major human pandemic.
20 potentially influenced by the 2009 influenza pandemic.
21 e been able to establish and maintain global pandemics.
22 en causing seasonal epidemics and occasional pandemics.
23 ans due to seasonal epidemics and occasional pandemics.
24 for stopping the obesity and type 2 diabetes pandemics.
25 broadens our understanding of the history of pandemics.
26 ccounting for numerous AHC outbreaks and two pandemics.
27 imes and from Indonesia once to cause global pandemics.
28 catastrophic, strong and moderate influenza pandemics.
29 ulation in the strong and moderate influenza pandemics.
30 catastrophic, strong and moderate influenza pandemics.
31 rden through seasonal epidemics and sporadic pandemics.
32 H2N2, and H3N2 subtypes have caused previous pandemics.
33 and influenza A viruses intermittently cause pandemics.
36 ve predecessor and the oseltamivir-resistant pandemic A H1N1 strain that emerged and circulated in Ja
37 vestigating potential adverse effects of the pandemic A(H1N1) vaccine have supported that influenza A
38 ion of alpha-GalCer to piglets infected with pandemic A/California/04/2009 (CA04) H1N1 IAV ameliorate
39 Furthermore, using human immune sera from pandemic A/California/04/2009 immune subjects and mAbs s
44 ence of mycoses is rising because of the HIV pandemic and because immunomodulatory drugs are increasi
45 f the world, and exacerbated by the HIV/AIDS pandemic and emergence of multidrug-resistant strains of
46 responses following challenge with H1N1 2009 pandemic and H3N2 viruses of mice that had been immunize
47 including the inferred ancestral viruses of pandemic and nonpandemic HIV-1 groups M (SIVcpzMB897) an
48 al and predictable, with the accuracy of pre-pandemic and real-time risk assessments hinging on relia
51 ical, especially with the prospect of future pandemics and for the effective development of a univers
52 widespread applications, from tracking virus pandemics and studying the macroevolutionary process of
53 subpopulation in the catastrophic influenza pandemic, and highest among the high-risk 0-19 years sub
54 accine to combat the hepatitis C virus (HCV) pandemic, and induction of broadly neutralizing monoclon
55 estral HIV-1 strains that founded the global pandemic, and very few complete genome sequences are ava
56 (IAV) causes annual epidemics and occasional pandemics, and is one of the best-characterized human RN
61 e monitored for emerging IAVs.IMPORTANCE IAV pandemics are caused by the introduction of novel viruse
65 ealth Organization (WHO) to declare the ZIKV pandemic as a Public Health Emergency of International C
66 rains from the GII.4 genotype causing serial pandemics as the virus evolves new ligand binding and an
68 Zika virus (ZIKV) has recently emerged as a pandemic associated with severe neuropathology in newbor
70 ent becomes the first line of defense during pandemics because there is insufficient time to produce
72 only the spring-summer timing of historical pandemics, but also early increases in pandemic severity
73 uenza A viruses can give rise to devastating pandemics, but currently it is impossible to predict the
76 r results consolidate historical accounts of pandemic cholera with data to show the importance of loc
78 s aureus (CA-MRSA) are the cause of a severe pandemic consisting primarily of skin and soft tissue in
80 id substitution that has been adopted by all pandemic CV-A24v strains and we reveal that this adaptat
82 The imminent threat of viral epidemics and pandemics dictates a need for therapeutic approaches tha
83 biotype is susceptible to CAMPs, but current pandemic El Tor biotype isolates gain CAMP resistance by
84 of intercontinental introductions of seventh pandemic El Tor V. cholerae and that at least seven line
85 cheap, safe and direct evidence relating to pandemic emergence, a field where indirect measurements
88 y pose the greatest threats for zoonotic and pandemic emergence.IMPORTANCE Avian influenza viruses, s
89 tion are urgently needed to combat potential pandemics, emerging viruses, and constantly mutating str
90 In 2009, the global outbreak of an influenza pandemic emphasized the need for an effective vaccine ad
93 t increased after the influenza A(H1N1) 2009 pandemic from 72% in 2010-2011 to 89% in 2014-2015 (P <
96 979 and 2010 to block glycan binding of four pandemic GII.4 noroviruses isolated in the last 4 decade
97 ed for at least 6 years against 3 decades of pandemic GII.4 NoV.IMPORTANCE Human noroviruses (NoVs) a
99 during natural coinfection of a patient with pandemic H1N1 (2009) and seasonal H1N1 influenza A virus
101 y coinfected with seasonal H1N1 (A/H1N1) and pandemic H1N1 (pdm/H1N1) during the Southern hemisphere
102 ssessed the public health risk of CIV-H3N2 x pandemic H1N1 (pdmH1N1) reassortants by characterizing t
103 luated the potential for viruses of the 2009 pandemic H1N1 (pH1N1) and seasonal H3N2 lineages to reas
105 sly shown that the NS1 protein from the 2009 pandemic H1N1 (pH1N1) virus is not able to inhibit gener
106 wn that the NS1 protein from this human 2009 pandemic H1N1 (pH1N1) virus was an effective interferon
107 th the PB2, NA, and M segments from the 2009 pandemic H1N1 (PH1N1) virus.In vitro and in vivo evaluat
108 d applies those tools to viruses of the 2009 pandemic H1N1 and seasonal H3N2 lineages, which currentl
109 st HAI response and protected mice against a pandemic H1N1 challenge were vaccines that contained the
112 ed with alum, the protective efficacy of the pandemic H1N1 influenza (pH1N1) vaccine was substantiall
115 ently characterized two swine viruses of the pandemic H1N1 lineage, A/swine/Virginia/1814-1/2012 (pH1
116 gglutinin was identified that increases 2009 pandemic H1N1 virus binding to human-like alpha2,6-linke
118 we show that distinct mutations in the 2009 pandemic H1N1 virus genome have occurred with increased
119 tibodies specific for the HA1 subunit of the pandemic H1N1 virus, and analyzed the correlation with t
121 During the 2015-16 influenza season, when pandemic H1N1 was the predominant virus, studies from th
122 tion of multiple IAV strains including H1N1, pandemic H1N1, H3N2 and H5N1, which supports the "wedge"
124 al vector expressing NA from avian (H5N1) or pandemic (H1N1) influenza virus, elicited NA-specific an
126 Our findings suggest that the 2009 influenza pandemic has an evident impact on the relative burden of
128 ructions in Bayesian phylogeography of virus pandemics have been improved by utilizing a Bayesian sto
130 o promote virus release from infected cells, pandemic HIV-1 group M strains evolved Vpu as a tetherin
131 rse primate lentiviruses including different pandemic HIV-1 group M subtypes for their ability to dow
132 from diverse primate lentiviruses including pandemic HIV-1 group M subtypes, we demonstrate that Nef
136 DC infected with seasonal IAV, but not with pandemic IAV, enhance maturation of uninfected DC and T
138 sentative group I (H5N1) and group II (H7N9) pandemic IAVs in mice and ferrets and could be used to b
139 s involved in the continually evolving HIV-1 pandemic.IMPORTANCE Very little is known about the ances
140 nt, which predate the first reported cholera pandemic in 1817, broadens our understanding of the hist
141 ses is important because H2 viruses caused a pandemic in 1957 and could cross into humans again.
147 ct of vaccine interventions during influenza pandemics in Chicago, and assist in vaccine intervention
148 tury [4]; and the most recent 19(th) century pandemic, in which Y. pestis spread worldwide [5] and be
149 veloped to indefinitely control the HIV/AIDS pandemic; in individual patients, these engineered molec
150 mplex 5 (A:cc5), has caused three successive pandemics, including epidemics in sub-Saharan Africa.
153 ine candidate expressing NA (PIV5-NA) from a pandemic influenza (pdmH1N1) virus or highly pathogenic
155 a mixing vessel for the generation of novel pandemic influenza A viruses through reassortment becaus
158 onfidence interval [CI], 2.61-6.13) for 2009 pandemic influenza A(H1N1) and 1.76 (95% CI, 1.33-2.32)
161 s season was characterized by a delayed 2009 pandemic influenza A(H1N1) virus (A[H1N1]pdm09) epidemic
162 3N2) virus infection (P = .002) but not 2009 pandemic influenza A(H1N1) virus (A[H1N1]pdm09) or influ
163 nfluenza season, nearly all circulating 2009 pandemic influenza A(H1N1) virus (A[H1N1]pdm09) strains
164 unit vaccine (ISV) targeting monovalent 2009 pandemic influenza A(H1N1) virus or live-attenuated infl
166 asonal influenza A/Panama/2007/99 (H3N2) and pandemic influenza A/Netherlands/602/2009 (H1N1) viruses
168 International Health Regulations (2005), and Pandemic Influenza Preparedness Framework-strives for a
170 le with multiple gene segments from the 2009 pandemic influenza virus strain without prior adaptation
171 HA protein is central to the emergence of a pandemic influenza virus, its required molecular propert
172 tween prior exposures to seasonal and recent pandemic influenza viruses and the development of hetero
174 In addition to seasonal infections, emerging pandemic influenza viruses present a continued threat to
183 n ST131, with accurate identification of the pandemic multidrug-resistant clonal subgroup ST131-H30.
186 Despite a large body of evidence showing the pandemic of chronic kidney disease, the impact of pre-op
192 Furthermore, IAVs can cause unpredictable pandemics of great consequence when viruses not previous
195 possibility of novel reassortants causing a pandemic outbreak necessitate the development of an anti
197 1.04% (95% CI: 0.15, 3.2) for the 2009 H1N1 pandemic, owing to the late timing of the vaccination pr
198 important source of influenza A virus (IAV) pandemics, owing to large, diverse viral reservoirs in p
199 ome highly pathogenic, raising concerns of a pandemic, particularly if these viruses acquire efficien
201 Eurasian avian-like (EA) swine H1N1 and 2009 pandemic (pdm/09) H1N1 viruses, reassortment between the
202 proportions of influenza B cases in the pre-pandemic period (2003-2008) negatively correlated with t
204 st that the highly pathogenic H7N9 virus has pandemic potential and should be closely monitored.
206 s and data sources, and assessed subnational pandemic potential for four viral haemorrhagic fevers in
208 lity of these viruses further highlights the pandemic potential of AIVs in the wild bird reservoir an
209 ut currently it is impossible to predict the pandemic potential of circulating avian influenza viruse
212 tment has implications for assessment of the pandemic potential of newly emerged influenza viruses, f
230 importance of developing an H10 vaccine for pandemic preparedness.IMPORTANCE Avian origin H10 influe
231 ccines against influenza virus and can guide pandemic-preparedness efforts directed against emerging
234 inistration, the government faced unexpected pandemics, ranging from the HIV/AIDS pandemic, which beg
236 AVs) cause seasonal epidemics and occasional pandemics, representing a serious public health concern.
238 with a focus on the epidemiology of the CPE pandemic; review risk factors for colonization and infec
244 andemic arose from a region not considered a pandemic risk, owing to an expansion of IAV diversity in
245 catastrophic, strong, and moderate influenza pandemic scenarios, due to their larger social contact n
246 rical pandemics, but also early increases in pandemic severity and multiple waves of transmission.
247 e analyse the time periods between influenza pandemics since 1700 under different assumptions to dete
250 es (T2D) has attained the status of a global pandemic, spreading from affluent industrialized nations
254 resistant to polymyxins, whereas a previous pandemic strain of the biotype Classical is polymyxin-se
255 mains unclear whether exposure to a previous pandemic strain stimulates immunity to a pandemic strain
256 c detection of particular strains, such as a pandemic strain versus a previous seasonal influenza, pl
257 le in the emergence of genetically "shifted" pandemic strains as well as its potential role as a cata
258 ns to determine whether the emergence of new pandemic strains is a memoryless or history-dependent pr
259 the natural history of GAS, the evolution of pandemic strains, and novel roles for several key virule
266 er of the human immunodeficiency virus (HIV) pandemic, the Democratic Republic of the Congo (DRC) is
267 Historically it was responsible for three pandemics: the Plague of Justinian in the 6(th) century
272 , and the scientific community to respond to pandemic threats when sufficient prior knowledge exists,
273 uses with the greatest risk of evolving into pandemic threats, and/or to understand drivers of such e
278 cine against seasonal influenza and emerging pandemic threats.IMPORTANCE Seasonal influenza viruses c
280 ng social disruption, being able, early in a pandemic, to immunize those who had received prepandemic
282 ly required, would reduce the total doses of pandemic vaccine then needed, extending vaccine supplies
283 ved prepandemic vaccine with one dose of the pandemic vaccine, rather than the 2 doses typically requ
284 e relationships between globally circulating pandemic Vibrio cholerae clones and local bacterial popu
287 virus reassortants resembling the 1918 human pandemic virus can become transmissible among mammals by
289 inin (HA) protein or reassortment with other pandemic viruses endow HPAI H5N1 viruses with the potent
291 human immunodeficiency virus type 1 (HIV-1) pandemic was ignited in Leopoldville (now known as Kinsh
292 To address the chikungunya fever (CHIKF) pandemic, we used an EILV cDNA clone to design a chimeri
293 ng (21.96%), and moderate (11.73%) influenza pandemics were compared against vaccine intervention sce
295 sporadic infections or spread worldwide in a pandemic when novel strains emerge in the human populati
296 xpected pandemics, ranging from the HIV/AIDS pandemic, which began during the Reagan administration,
297 large-scale antiviral interventions during a pandemic with co-circulation of AVS and AVR strains, our
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