Database : MEDLINE
Search on : caliciviridae and infections [Words]
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[PMID]: 28461205
[Au] Autor:Supadej K; Khamrin P; Kumthip K; Kochjan P; Yodmeeklin A; Ushijima H; Maneekarn N
[Ad] Address:Department of Microbiology, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand.
[Ti] Title:Wide variety of recombinant strains of norovirus GII in pediatric patients hospitalized with acute gastroenteritis in Thailand during 2005 to 2015.
[So] Source:Infect Genet Evol;52:44-51, 2017 Aug.
[Is] ISSN:1567-7257
[Cp] Country of publication:Netherlands
[La] Language:eng
[Ab] Abstract:Norovirus (NoV) has been reported as being a common cause of acute gastroenteritis both in children and adults worldwide. Of the many variants, NoV GII.4 is the most predominant genotype. One of the mechanisms that drives the evolution and emergence of new variants of NoV is homologous recombination. This study describes the genetic recombination involved in cases of NoV GII detected in pediatric patients with acute gastroenteritis in Chiang Mai, Thailand during 2005 to 2015. From a total of 1938 stool samples, 3 (0.15%) were positive for NoV GI and 298 (15.38%) were identified as NoV GII. The genotypes detected in this study were GI.6, GI.14, GII.1, GII.2, GII.3, GII.4, GII.6, GII.7, GII.12, GII.13, GII.14, GII.15, GII.16, GII.17, GII.20, and GII.21. The NoV recombinant strains were verified by analysis of the partial sequence of ORF1 (RdRp)/ORF2 (capsid) junction. Phylogenetic analyses of partial ORF1 and ORF2 regions resulted in the identification of 21 (6.98%) NoV recombinant strains. Among these, 9 recombination patterns were detected in this study; GII.Pe/GII.4, GII.Pg/GII.1, GII.Pg/GII.12, GII.P7/GII.6, GII.P7/GII.14, GII.P12/GII.4, GII.P16/GII.2, GII.P16/GII.13, and GII.P21/GII.3. The findings demonstrated the wide variety of recombinant strains of NoV GII strains detected in pediatric patients admitted to the hospitals with acute gastroenteritis in Chiang Mai, Thailand during the past decade.
[Mh] MeSH terms primary: Caliciviridae Infections/diagnosis
Gastroenteritis/virology
Norovirus/genetics
[Mh] MeSH terms secundary: Child
Evolution, Molecular
Genotype
Hospitalization
Humans
Norovirus/classification
Phylogeny
Recombination, Genetic
Thailand
[Pt] Publication type:JOURNAL ARTICLE
[Em] Entry month:1803
[Cu] Class update date: 180309
[Lr] Last revision date:180309
[Js] Journal subset:IM
[Da] Date of entry for processing:170503
[St] Status:MEDLINE

  2 / 3523 MEDLINE  
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[PMID]: 28450084
[Au] Autor:Bodnar L; Lorusso E; Di Martino B; Catella C; Lanave G; Elia G; Bányai K; Buonavoglia C; Martella V
[Ad] Address:University Aldo Moro of Bari, Valenzano, Italy.
[Ti] Title:Identification of a novel canine norovirus.
[So] Source:Infect Genet Evol;52:75-81, 2017 Aug.
[Is] ISSN:1567-7257
[Cp] Country of publication:Netherlands
[La] Language:eng
[Ab] Abstract:By screening a collection of fecal samples from young dogs from different European countries, noroviruses (NoVs) were found in 13/294 (4.4%) animals with signs of enteritis whilst they were not detected in healthy dogs (0/42). An informative portion of the genome (3.4kb at the 3' end) was generated for four NoV strains. In the capsid protein VP1 region, strains 63.15/2015/ITA and FD53/2007/ITA were genetically related to the canine GVI.2 strain C33/Viseu/2007/PRT (97.4-98.6% nt and 90.3-98.6% aa). Strain FD210/2007/ITA displayed the highest identity to the GVI.1 canine strain Bari/91/2007/ITA (88.0% nt and 95.0% aa). Strain 5010/2009/ITA displayed only 66.6-67.6% nt and 75.5-81.6% aa identities to the GVI.1 canine strains FD210/2007/ITA and Bari/91/2007/ITA and the GVI feline strain M49-1/2012/JPN. Identity to the other canine/feline NoVs strains in the VP1 was lower than 67.6% nt and 62.7% aa. Based on the full-length VP1 amino acid sequence and the criteria proposed for distinction of NoV genotypes, the canine NoV 5010/2009/ITA could represent the prototype of a third GVI genotype, thus providing further evidence for the genetic heterogeneity of NoVs in carnivores.
[Mh] MeSH terms primary: Caliciviridae Infections/veterinary
Dog Diseases/virology
Gastroenteritis/veterinary
Norovirus/classification
[Mh] MeSH terms secundary: Animals
Caliciviridae Infections/diagnosis
Caliciviridae Infections/epidemiology
Dog Diseases/epidemiology
Dogs
Europe/epidemiology
Evolution, Molecular
Feces/virology
Gastroenteritis/virology
Genome, Viral
Norovirus/genetics
Norovirus/isolation & purification
Phylogeny
Sequence Analysis, RNA
[Pt] Publication type:JOURNAL ARTICLE
[Em] Entry month:1803
[Cu] Class update date: 180309
[Lr] Last revision date:180309
[Js] Journal subset:IM
[Da] Date of entry for processing:170429
[St] Status:MEDLINE

  3 / 3523 MEDLINE  
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[PMID]: 28453838
[Au] Autor:Lindesmith LC; Mallory ML; Jones TA; Richardson C; Goodwin RR; Baehner F; Mendelman PM; Bargatze RF; Baric RS
[Ad] Address:Department of Epidemiology, University of North Carolina, Chapel Hill, NC, USA.
[Ti] Title:Impact of Pre-exposure History and Host Genetics on Antibody Avidity Following Norovirus Vaccination.
[So] Source:J Infect Dis;215(6):984-991, 2017 03 15.
[Is] ISSN:1537-6613
[Cp] Country of publication:United States
[La] Language:eng
[Ab] Abstract:Background: Development of high avidity, broadly neutralizing antibodies (Abs) is a priority after vaccination against rapidly evolving, widely disseminated viruses like human norovirus. After vaccination with a multivalent GI.1 and GII.4c norovirus virus-like particle (VLP) vaccine candidate adjuvanted with alum and monophosphoryl lipid A (MPL), blockade Ab titers peaked early, with no increase in titer following a second vaccine dose. Methods: Blockade Ab relative avidity was evaluated by measuring the slope of blockade Ab neutralization curves. Results: Blockade Ab avidity to the GI.1 vaccine component peaked at day 35 (7 days after dose 2). Avidities to heterotypic genogroup I VLPs were not sustained at day 35 after vaccination or GI.1 infection, as measured from archived sera. Only secretor-positive participants maintained high avidity blockade Ab to GI.1 at day 180. Avidity to the GII.4c vaccine component peaked at day 7, remained elevated through day 180, and was not secretor dependent. Avidity to an immunologically novel GII.4 strain VLP correlated with preexisting Ab titer to an ancestral strain Epitope A. Conclusions: Host genetics and pre-exposure history shape norovirus vaccine Ab responses, including blockade Ab avidity. Avidity of potentially neutralizing Ab may be an important metric for evaluating vaccine responses to highly penetrant viruses with cross-reactive serotypes.
[Mh] MeSH terms primary: Antibody Affinity
Caliciviridae Infections/prevention & control
Vaccines, Virus-Like Particle/therapeutic use
Viral Vaccines/therapeutic use
[Mh] MeSH terms secundary: Adjuvants, Immunologic/administration & dosage
Adolescent
Adult
Aged
Aged, 80 and over
Antibodies, Neutralizing/blood
Antibodies, Viral/blood
Caliciviridae Infections/genetics
Cross Reactions
Double-Blind Method
Epitopes/immunology
Female
Humans
Male
Middle Aged
Norovirus
United States
Vaccination
Vaccines, Virus-Like Particle/administration & dosage
Viral Vaccines/administration & dosage
Young Adult
[Pt] Publication type:CLINICAL TRIAL, PHASE I; JOURNAL ARTICLE; MULTICENTER STUDY; RANDOMIZED CONTROLLED TRIAL
[Nm] Name of substance:0 (Adjuvants, Immunologic); 0 (Antibodies, Neutralizing); 0 (Antibodies, Viral); 0 (Epitopes); 0 (Vaccines, Virus-Like Particle); 0 (Viral Vaccines)
[Em] Entry month:1706
[Cu] Class update date: 180308
[Lr] Last revision date:180308
[Js] Journal subset:AIM; IM
[Da] Date of entry for processing:170429
[St] Status:MEDLINE
[do] DOI:10.1093/infdis/jix045

  4 / 3523 MEDLINE  
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[PMID]: 29471848
[Au] Autor:Binn LN; Norby EA; Marchwicki RH; Jarman RG; Keiser PB; Hang J
[Ad] Address:Viral Diseases Branch, Walter Reed Army Institute of Research, Silver Spring, MD, 20910, USA. leonard.n.binn.vol@mail.mil.
[Ti] Title:Canine caliciviruses of four serotypes from military and research dogs recovered in 1963-1978 belong to two phylogenetic clades in the Vesivirus genus.
[So] Source:Virol J;15(1):39, 2018 Feb 23.
[Is] ISSN:1743-422X
[Cp] Country of publication:England
[La] Language:eng
[Ab] Abstract:BACKGROUND: Vesiviruses (family Caliciviridae) had been shown capable of invading a variety of host species, raising concern of their zoonotic potential. Since the 1980's, several canine caliciviruses (CaCV) isolates have been reported and are phylogenetically related to the vesiviruses with features distinct from both Vesicular exanthema of swine virus (VESV) and Feline calicivirus (FCV) species in phylogeny, serology and cell culture specificities. Etiological studies of canine diseases in dogs used for military services and laboratory studies were conducted in 1963-1978 at the Walter Reed Army Institute of Research. Multiple known and unknown viral pathogens including caliciviruses were recovered. METHODS: Four unidentified isolates were recovered in Walter Reed Canine Cells (WRCC) from respiratory, fecal and penile specimens. Physicochemical tests, electron microscopy, viral cultivation in human and animal cells, antibody neutralization assays, and recently the genome sequencing were used to characterize the isolates. Sera from these dogs and their cohorts were tested with the isolates to determine origin and prevalence of the infections. RESULTS: The viral isolates were small non-enveloped spherical RNA virions, 27 to 42 nm in diameter with cup-like structures, indicating they are caliciviruses. They propagated in WRCC and MDCK cells, not in either other canine cells or human and other animal cells. Each isolate is antigenically distinct and react with dog sera in respective cohorts. The genomes have nucleotide identities ranging from 70.3% to 90.7% and encode the non-structural polyprotein (1810 amino acids), major capsid protein (691 amino acids) and minor structural protein (134 amino acids). They belong to two different phylogenetic clades in Vesivirus genus with close relation with canine calicivirus (CaCV). CONCLUSIONS: These CaCV isolates have restricted cell tropism, antigenic diversity and genetic variation. Further investigation will shed light on antigenic relation to other vesiviruses, and its pathogenicity for dogs and potential infectivity to other animals. Together with the previously reported CaCV strains provides significant evidence to support the formation of a new CaCV species in the Vesivirus genus.
[Pt] Publication type:JOURNAL ARTICLE
[Em] Entry month:1802
[Cu] Class update date: 180227
[Lr] Last revision date:180227
[St] Status:In-Data-Review
[do] DOI:10.1186/s12985-018-0944-4

  5 / 3523 MEDLINE  
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[PMID]: 29440610
[Au] Autor:Harcourt-Brown N; Harcourt-Brown F
[Ad] Address:30 Crab Lane, Bilton, Harrogate, North Yorkshire HG1 3BE.
[Ti] Title:Preventing rabbit haemorrhagic disease.
[So] Source:Vet Rec;182(6):172-173, 2018 02 10.
[Is] ISSN:2042-7670
[Cp] Country of publication:England
[La] Language:eng
[Mh] MeSH terms primary: Caliciviridae Infections/prevention & control
Hemorrhagic Disease Virus, Rabbit
[Mh] MeSH terms secundary: Animals
Hemorrhagic Disorders
Rabbits
[Pt] Publication type:LETTER; COMMENT
[Em] Entry month:1802
[Cu] Class update date: 180223
[Lr] Last revision date:180223
[Js] Journal subset:IM
[Da] Date of entry for processing:180215
[St] Status:MEDLINE
[do] DOI:10.1136/vr.k576

  6 / 3523 MEDLINE  
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[PMID]: 28449729
[Au] Autor:Bidalot M; Théry L; Kaplon J; De Rougemont A; Ambert-Balay K
[Ad] Address:National Reference Centre for Gastroenteritis Viruses, Laboratory of Biology and Pathology, University Hospital Dijon Bourgogne, Dijon, France.
[Ti] Title:Emergence of new recombinant noroviruses GII.p16-GII.4 and GII.p16-GII.2, France, winter 2016 to 2017.
[So] Source:Euro Surveill;22(15), 2017 Apr 13.
[Is] ISSN:1560-7917
[Cp] Country of publication:Sweden
[La] Language:eng
[Ab] Abstract:An early increase in outbreaks of norovirus gastroenteritis characterised at the French National Reference Centre occurred this winter season. They were concurrent with an unusual pattern of circulating strains, with three predominant genotypes: the re-emergent variant GII.P4 2009-GII.4 2012 found in 28% of norovirus outbreaks and two new emergent recombinant strains GII.P16-GII.4 2012 and GII.P16-GII.2 never before observed in France, found in 24% and 14% of norovirus outbreaks, respectively.
[Mh] MeSH terms primary: Caliciviridae Infections/virology
Communicable Diseases, Emerging/epidemiology
Communicable Diseases, Emerging/virology
Gastroenteritis/epidemiology
Gastroenteritis/virology
Norovirus/genetics
Seasons
[Mh] MeSH terms secundary: Caliciviridae Infections/epidemiology
Feces/virology
France/epidemiology
Humans
Norovirus/isolation & purification
Reassortant Viruses/genetics
Reassortant Viruses/isolation & purification
[Pt] Publication type:JOURNAL ARTICLE
[Em] Entry month:1802
[Cu] Class update date: 180220
[Lr] Last revision date:180220
[Js] Journal subset:IM
[Da] Date of entry for processing:170429
[St] Status:MEDLINE

  7 / 3523 MEDLINE  
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[PMID]: 29024672
[Au] Autor:Dalton KP; Arnal JL; Benito AA; Chacón G; Martín Alonso JM; Parra F
[Ad] Address:Instituto Universitario de Biotecnología de Asturias, Universidad de Oviedo, Oviedo, Spain. Electronic address: daltonkevin@uniovi.es.
[Ti] Title:Conventional and real time RT-PCR assays for the detection and differentiation of variant rabbit hemorrhagic disease virus (RHDVb) and its recombinants.
[So] Source:J Virol Methods;251:118-122, 2018 Jan.
[Is] ISSN:1879-0984
[Cp] Country of publication:Netherlands
[La] Language:eng
[Ab] Abstract:Since its emergence, variant RHDV (RHDVb/RHDV2) has spread throughout the Iberian Peninsula aided by the apparent lack of cross protection provided by classic (genogroup 1; G1) strain derived vaccines. In addition to RHDVb, full-length genome sequencing of RHDV strains has recently revealed the circulation of recombinant viruses on the Iberian Peninsula. These recombinant viruses contain the RHDVb structural protein encoding sequences and the non-structural coding regions of either pathogenic RHDV-G1 strains or non-pathogenic (np) rabbit caliciviruses. The aim of the work was twofold: firstly to validate a diagnostic real time RT-PCR developed in 2012 for the detection of RHDVb strains and secondly, to design a conventional RT-PCR for the differentiation of RHDVb strains from RHDVb recombinants by subsequent sequencing of the amplicon.
[Mh] MeSH terms primary: Caliciviridae Infections/veterinary
Genetic Variation
Hemorrhagic Disease Virus, Rabbit/classification
Hemorrhagic Disease Virus, Rabbit/isolation & purification
Polymerase Chain Reaction/methods
Rabbits/virology
[Mh] MeSH terms secundary: Animals
Caliciviridae Infections/virology
Hemorrhagic Disease Virus, Rabbit/genetics
Recombination, Genetic
Spain
[Pt] Publication type:JOURNAL ARTICLE; VALIDATION STUDIES
[Em] Entry month:1802
[Cu] Class update date: 180201
[Lr] Last revision date:180201
[Js] Journal subset:IM
[Da] Date of entry for processing:171013
[St] Status:MEDLINE

  8 / 3523 MEDLINE  
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[PMID]: 28986291
[Au] Autor:Meli ML; Berger A; Willi B; Spiri AM; Riond B; Hofmann-Lehmann R
[Ad] Address:Clinical Laboratory, Vetsuisse Faculty, University of Zurich, Zurich, Switzerland; Center for Clinical Studies, Vetsuisse Faculty, University of Zurich, Zurich, Switzerland. Electronic address: mmeli@vetclinics.uzh.ch.
[Ti] Title:Molecular detection of feline calicivirus in clinical samples: A study comparing its detection by RT-qPCR directly from swabs and after virus isolation.
[So] Source:J Virol Methods;251:54-60, 2018 Jan.
[Is] ISSN:1879-0984
[Cp] Country of publication:Netherlands
[La] Language:eng
[Ab] Abstract:Feline caliciviruses (FCVs) are non-enveloped RNA viruses that exhibit high genetic variation. Two reverse transcription quantitative polymerase chain reaction (RT-qPCR) FCV assays (S1 and S2) were evaluated using samples from 300 field cats. The direct detection of FCV in swabs and after propagation in cell culture, as well as the influence of storage conditions, was assessed. FCV-RNA detectability on dry swabs was similar after storage at either 4°C or -20°C, but viral burdens were maintained for a longer time period when viral transport medium was used. A total of 97 (32%) samples was considered FCV PCR-positive. Of these, 81% and 77% tested positive directly from swabs using S1 and S2, respectively; 84% and 81% tested positive after enrichment in cell culture, respectively. Combined detection by RT-PCR directly from swabs and after VI was most sensitive (up to 96%). Neither of the methods alone were able to detect all FCV-positive samples. In conclusion, clinical samples should be collected in viral transport medium, stored at ≤4°C and processed as soon as possible. The combination of cell culture with RT-qPCR or detection directly from swabs using a combination of different RT-qPCR assays is recommended to reach a high sensitivity of FCV detection.
[Mh] MeSH terms primary: Caliciviridae Infections/veterinary
Calicivirus, Feline/isolation & purification
Cat Diseases/diagnosis
Cat Diseases/virology
Molecular Diagnostic Techniques/methods
Real-Time Polymerase Chain Reaction/methods
Specimen Handling/methods
[Mh] MeSH terms secundary: Animals
Caliciviridae Infections/diagnosis
Caliciviridae Infections/virology
Cats
Sensitivity and Specificity
Virus Cultivation
[Pt] Publication type:COMPARATIVE STUDY; EVALUATION STUDIES; JOURNAL ARTICLE
[Em] Entry month:1802
[Cu] Class update date: 180201
[Lr] Last revision date:180201
[Js] Journal subset:IM
[Da] Date of entry for processing:171008
[St] Status:MEDLINE

  9 / 3523 MEDLINE  
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[PMID]: 28941616
[Au] Autor:Dalton KP; Podadera A; Granda V; Nicieza I; Del Llano D; González R; de Los Toyos JR; García Ocaña M; Vázquez F; Martín Alonso JM; Prieto JM; Parra F; Casais R
[Ad] Address:Instituto Universitario de Biotecnología de Asturias, Departamento de Bioquímica y Biología Molecular, Edificio Santiago Gascón, Universidad de Oviedo, Campus El Cristo, 33006, Oviedo, Spain. Electronic address: daltonkevin@uniovi.es.
[Ti] Title:ELISA for detection of variant rabbit haemorrhagic disease virus RHDV2 antigen in liver extracts.
[So] Source:J Virol Methods;251:38-42, 2018 Jan.
[Is] ISSN:1879-0984
[Cp] Country of publication:Netherlands
[La] Language:eng
[Ab] Abstract:The emergence and rapid spread of variant of the rabbit hemorrhagic disease virus (RHDV2) require new diagnostic tools to ensure that efficient control measures are adopted. In the present study, a specific sandwich enzyme-linked immunosorbent assay (ELISA) for detection of RHDV2 antigens in rabbit liver homogenates, based on the use of an RHDV2-specific monoclonal antibody (Mab) 2D9 for antigen capture and an anti-RHDV2 goat polyclonal antibody (Pab), was developed. This ELISA was able to successfully detect RHDV2 and RHDV2 recombinant virions with high sensitivity (100%) and specificity (97.22%). No cross-reactions were detected with RHDV G1 viruses while low cross-reactivity was detected with one of the RHDVa samples analyzed. The ELISA afforded good repeatability and had high analytical sensitivity as it was able to detect a dilution 1:163,640 (6.10ng/mL) of purified RHDV-N11 VLPs, which contained approximately 3.4×10 molecules/mL particles. The reliable discrimination between closely related viruses is crucial to understand the epidemiology and the interaction of co-existing pathogens. In the work described here we design and validate an ELISA for laboratory based, specific, sensitive and reliable detection of RHDVb/RHDV2. This ELISA is a valuable, specific virological tool for monitoring virus circulation, which will permit a better control of this disease.
[Mh] MeSH terms primary: Antigens, Viral/analysis
Caliciviridae Infections/veterinary
Diagnostic Tests, Routine/methods
Enzyme-Linked Immunosorbent Assay/methods
Hemorrhagic Disease Virus, Rabbit/isolation & purification
Liver/virology
[Mh] MeSH terms secundary: Animals
Antigens, Viral/immunology
Caliciviridae Infections/diagnosis
Caliciviridae Infections/virology
Cross Reactions
Hemorrhagic Disease Virus, Rabbit/immunology
Reproducibility of Results
Sensitivity and Specificity
Veterinary Medicine/methods
[Pt] Publication type:EVALUATION STUDIES; JOURNAL ARTICLE
[Nm] Name of substance:0 (Antigens, Viral)
[Em] Entry month:1802
[Cu] Class update date: 180201
[Lr] Last revision date:180201
[Js] Journal subset:IM
[Da] Date of entry for processing:170925
[St] Status:MEDLINE

  10 / 3523 MEDLINE  
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[PMID]: 29284004
[Au] Autor:Fu JG; Shi C; Xu C; Lin Q; Zhang J; Yi QH; Zhang J; Bao CJ; Huo X; Zhu YF; Ai J; Xing Z
[Ad] Address:Medical School and Jiangsu Key Laboratory of Molecular Medicine, Nanjing University, Nanjing, China.
[Ti] Title:Outbreaks of acute gastroenteritis associated with a re-emerging GII.P16-GII.2 norovirus in the spring of 2017 in Jiangsu, China.
[So] Source:PLoS One;12(12):e0186090, 2017.
[Is] ISSN:1932-6203
[Cp] Country of publication:United States
[La] Language:eng
[Ab] Abstract:A total of 64 acute gastroenteritis outbreaks with 2,953 patients starting in December of 2016 and occurring mostly in the late spring of 2017 were reported in Jiangsu, China. A recombinant GII.P16-GII.2 norovirus variant was associated with 47 outbreaks (73.4%) for the gastroenteritis epidemic, predominantly occurring in February and March of 2017. Sequence analysis of the RNA-dependent RNA polymerase (RdRp) and capsid protein of the viral isolates from these outbreaks confirmed that this GII.P16-GII.2 strain was the GII.P16-GII.2 variant with the intergenotypic recombination, identified in Taiwan, Hong Kong, and other cities in China in 2016. This GII.P16-GII.2 recombinant variant appeared to a re-emerging strain, firstly identified in 2011-2012 from Japan and USA but might be independently originated from other GII.P16-GII.2 variants for sporadic and outbreaks of gastroenteritis in Japan and China before 2016. Further identification of unique amino acid mutations in both VP1 and RdRp of NoV strain as shown in this report may provide insight in explaining its structural and antigenic changes, potentially critical for the variant recombinant to gain its predominance in causing regional and worldwide epidemics.
[Mh] MeSH terms primary: Caliciviridae Infections/epidemiology
Disease Outbreaks
Gastroenteritis/epidemiology
Norovirus/isolation & purification
[Mh] MeSH terms secundary: Acute Disease
China/epidemiology
Genes, Viral
Humans
Norovirus/classification
Norovirus/genetics
Norovirus/pathogenicity
Phylogeny
Viral Proteins/genetics
[Pt] Publication type:JOURNAL ARTICLE; RESEARCH SUPPORT, NON-U.S. GOV'T
[Nm] Name of substance:0 (Viral Proteins)
[Em] Entry month:1801
[Cu] Class update date: 180129
[Lr] Last revision date:180129
[Js] Journal subset:IM
[Da] Date of entry for processing:171229
[St] Status:MEDLINE
[do] DOI:10.1371/journal.pone.0186090


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