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1.
PLoS Negl Trop Dis ; 13(7): e0007473, 2019 07.
Artigo em Inglês | MEDLINE | ID: mdl-31306420

RESUMO

The N-linked glycosylation motif at amino acid position 154-156 of the envelope (E) protein of West Nile virus (WNV) is linked to enhanced murine neuroinvasiveness, avian pathogenicity and vector competence. Naturally occurring isolates with altered E protein glycosylation patterns have been observed in WNV isolates; however, the specific effects of these polymorphisms on avian host pathogenesis and vector competence have not been investigated before. In the present study, amino acid polymorphisms, NYT, NYP, NYF, SYP, SYS, KYS and deletion (A'DEL), were reverse engineered into a parental WNV (NYS) cDNA infectious clone to generate WNV glycosylation mutant viruses. These WNV glycosylation mutant viruses were characterized for in vitro growth, pH-sensitivity, temperature-sensitivity and host competence in American crows (AMCR), house sparrows (HOSP) and Culex quinquefasciatus. The NYS and NYT glycosylated viruses showed higher viral replication, and lower pH and temperature sensitivity than NYP, NYF, SYP, SYS, KYS and A'DEL viruses in vitro. Interestingly, in vivo results demonstrated asymmetric effects in avian and mosquito competence that were independent of the E-protein glycosylation status. In AMCRs and HOSPs, all viruses showed comparable viremias with the exception of NYP and KYS viruses that showed attenuated phenotypes. Only NYP showed reduced vector competence in both Cx. quinquefasciatus and Cx. tarsalis. Glycosylated NYT exhibited similar avian virulence properties as NYS, but resulted in higher mosquito oral infectivity than glycosylated NYS and nonglycosylated, NYP, NYF, SYP and KYS mutants. These data demonstrated that amino acid polymorphisms at E154/156 dictate differential avian host and vector competence phenotypes independent of E-protein glycosylation status.


Assuntos
Vetores de Doenças , Proteínas do Envelope Viral/metabolismo , Febre do Nilo Ocidental/virologia , Vírus do Nilo Ocidental/metabolismo , Aedes , Motivos de Aminoácidos , Animais , Chlorocebus aethiops , Culex/virologia , Culicidae/virologia , Modelos Animais de Doenças , Feminino , Glicosilação , Concentração de Íons de Hidrogênio , Camundongos , Mutação , Fenótipo , Pardais/virologia , Células Vero , Proteínas do Envelope Viral/genética , Viremia , Virulência , Replicação Viral , Vírus do Nilo Ocidental/genética
2.
Arch Virol ; 164(7): 1949-1965, 2019 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-31065850

RESUMO

In February 2019, following the annual taxon ratification vote, the order Bunyavirales was amended by creation of two new families, four new subfamilies, 11 new genera and 77 new species, merging of two species, and deletion of one species. This article presents the updated taxonomy of the order Bunyavirales now accepted by the International Committee on Taxonomy of Viruses (ICTV).


Assuntos
Bunyaviridae/classificação , Bunyaviridae/genética , Genoma Viral/genética , Filogenia , RNA Viral/genética
3.
Arch Virol ; 164(3): 927-941, 2019 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-30663021

RESUMO

In October 2018, the order Bunyavirales was amended by inclusion of the family Arenaviridae, abolishment of three families, creation of three new families, 19 new genera, and 14 new species, and renaming of three genera and 22 species. This article presents the updated taxonomy of the order Bunyavirales as now accepted by the International Committee on Taxonomy of Viruses (ICTV).


Assuntos
Arenaviridae/classificação , Animais , Arenaviridae/genética , Arenaviridae/isolamento & purificação , Infecções por Arenaviridae/virologia , Humanos , Filogenia
4.
PLoS Negl Trop Dis ; 12(2): e0006302, 2018 02.
Artigo em Inglês | MEDLINE | ID: mdl-29447156

RESUMO

West Nile virus (WNV) and St. Louis encephalitis (SLEV) virus are enzootically maintained in North America in cycles involving the same mosquito vectors and similar avian hosts. However, these viruses exhibit dissimilar viremia and virulence phenotypes in birds: WNV is associated with high magnitude viremias that can result in mortality in certain species such as American crows (AMCRs, Corvus brachyrhynchos) whereas SLEV infection yields lower viremias that have not been associated with avian mortality. Cross-neutralization of these viruses in avian sera has been proposed to explain the reduced circulation of SLEV since the introduction of WNV in North America; however, in 2015, both viruses were the etiologic agents of concurrent human encephalitis outbreaks in Arizona, indicating the need to re-evaluate host factors and cross-neutralization responses as factors potentially affecting viral co-circulation. Reciprocal chimeric WNV and SLEV viruses were constructed by interchanging the pre-membrane (prM)-envelope (E) genes, and viruses subsequently generated were utilized herein for the inoculation of three different avian species: house sparrows (HOSPs; Passer domesticus), house finches (Haemorhous mexicanus) and AMCRs. Cross-protective immunity between parental and chimeric viruses were also assessed in HOSPs. Results indicated that the prM-E genes did not modulate avian replication or virulence differences between WNV and SLEV in any of the three avian species. However, WNV-prME proteins did dictate cross-protective immunity between these antigenically heterologous viruses. Our data provides further evidence of the important role that the WNV / SLEV viral non-structural genetic elements play in viral replication, avian host competence and virulence.


Assuntos
Doenças das Aves/virologia , Vírus da Encefalite de St. Louis/genética , Encefalite Viral/veterinária , Febre do Nilo Ocidental/veterinária , Vírus do Nilo Ocidental/genética , Animais , Doenças das Aves/imunologia , Doenças das Aves/mortalidade , Doenças das Aves/transmissão , Proteção Cruzada/imunologia , Corvos/virologia , Vírus da Encefalite de St. Louis/imunologia , Vírus da Encefalite de St. Louis/fisiologia , Encefalite Viral/imunologia , Encefalite Viral/transmissão , Encefalite Viral/virologia , Tentilhões/virologia , Interações Hospedeiro-Patógeno , Humanos , Fenótipo , Pardais/virologia , Proteínas não Estruturais Virais/genética , Proteínas não Estruturais Virais/imunologia , Viremia , Virulência/genética , Replicação Viral , Febre do Nilo Ocidental/imunologia , Febre do Nilo Ocidental/transmissão , Febre do Nilo Ocidental/virologia , Vírus do Nilo Ocidental/imunologia , Vírus do Nilo Ocidental/fisiologia
5.
PLoS Negl Trop Dis ; 10(8): e0004938, 2016 08.
Artigo em Inglês | MEDLINE | ID: mdl-27548738

RESUMO

West Nile virus (WNV) replicates in a wide variety of avian species, which serve as reservoir and amplification hosts. WNV strains isolated in North America, such as the prototype strain NY99, elicit a highly pathogenic response in certain avian species, notably American crows (AMCRs; Corvus brachyrhynchos). In contrast, a closely related strain, KN3829, isolated in Kenya, exhibits a low viremic response with limited mortality in AMCRs. Previous work has associated the difference in pathogenicity primarily with a single amino acid mutation at position 249 in the helicase domain of the NS3 protein. The NY99 strain encodes a proline residue at this position, while KN3829 encodes a threonine. Introduction of an NS3-T249P mutation in the KN3829 genetic background significantly increased virulence and mortality; however, peak viremia and mortality were lower than those of NY99. In order to elucidate the viral genetic basis for phenotype variations exclusive of the NS3-249 polymorphism, chimeric NY99/KN3829 viruses were created. We show herein that differences in the NS1-2B region contribute to avian pathogenicity in a manner that is independent of and additive with the NS3-249 mutation. Additionally, NS1-2B residues were found to alter temperature sensitivity when grown in avian cells.


Assuntos
Aves/virologia , Polimorfismo Genético , Proteínas não Estruturais Virais/genética , Vírus do Nilo Ocidental/genética , Vírus do Nilo Ocidental/patogenicidade , Animais , Doenças das Aves/virologia , Quênia/epidemiologia , Mutação , América do Norte/epidemiologia , Temperatura , Viremia , Virulência/genética , Replicação Viral , Febre do Nilo Ocidental/epidemiologia , Febre do Nilo Ocidental/virologia , Vírus do Nilo Ocidental/fisiologia
6.
PLoS One ; 11(1): e0147962, 2016.
Artigo em Inglês | MEDLINE | ID: mdl-26807734

RESUMO

Collection of mosquitoes and testing for vector-borne viruses is a key surveillance activity that directly influences the vector control efforts of public health agencies, including determining when and where to apply insecticides. Vector control districts in California routinely monitor for three human pathogenic viruses including West Nile virus (WNV), Western equine encephalitis virus (WEEV), and St. Louis encephalitis virus (SLEV). Reverse transcription quantitative polymerase chain reaction (RT-qPCR) offers highly sensitive and specific detection of these three viruses in a single multiplex reaction, but this technique requires costly, specialized equipment that is generally only available in centralized public health laboratories. We report the use of reverse transcription loop-mediated isothermal amplification (RT-LAMP) to detect WNV, WEEV, and SLEV RNA extracted from pooled mosquito samples collected in California, including novel primer sets for specific detection of WEEV and SLEV, targeting the nonstructural protein 4 (nsP4) gene of WEEV and the 3' untranslated region (3'-UTR) of SLEV. Our WEEV and SLEV RT-LAMP primers allowed detection of <0.1 PFU/reaction of their respective targets in <30 minutes, and exhibited high specificity without cross reactivity when tested against a panel of alphaviruses and flaviviruses. Furthermore, the SLEV primers do not cross-react with WNV, despite both viruses being closely related members of the Japanese encephalitis virus complex. The SLEV and WEEV primers can also be combined in a single RT-LAMP reaction, with discrimination between amplicons by melt curve analysis. Although RT-qPCR is approximately one order of magnitude more sensitive than RT-LAMP for all three targets, the RT-LAMP technique is less instrumentally intensive than RT-qPCR and provides a more cost-effective method of vector-borne virus surveillance.


Assuntos
Culicidae/virologia , Vírus da Encefalite de St. Louis/isolamento & purificação , Vírus da Encefalite Equina do Oeste/isolamento & purificação , Vírus do Nilo Ocidental/isolamento & purificação , Animais , Primers do DNA , Humanos , Técnicas de Amplificação de Ácido Nucleico , Vigilância da População , Sensibilidade e Especificidade
7.
J Gen Virol ; 95(Pt 12): 2796-2808, 2014 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-25146007

RESUMO

In the past decade, there has been an upsurge in the number of newly described insect-specific flaviviruses isolated pan-globally. We recently described the isolation of a novel flavivirus (tentatively designated 'Nhumirim virus'; NHUV) that represents an example of a unique subset of apparently insect-specific viruses that phylogenetically affiliate with dual-host mosquito-borne flaviviruses despite appearing to be limited to replication in mosquito cells. We characterized the in vitro growth potential and 3' untranslated region (UTR) sequence homology with alternative flaviviruses, and evaluated the virus's capacity to suppress replication of representative Culex spp.-vectored pathogenic flaviviruses in mosquito cells. Only mosquito cell lines were found to support NHUV replication, further reinforcing the insect-specific phenotype of this virus. Analysis of the sequence and predicted RNA secondary structures of the 3' UTR indicated NHUV to be most similar to viruses within the yellow fever serogroup and Japanese encephalitis serogroup, and viruses in the tick-borne flavivirus clade. NHUV was found to share the fewest conserved sequence elements when compared with traditional insect-specific flaviviruses. This suggests that, despite apparently being insect specific, this virus probably diverged from an ancestral mosquito-borne flavivirus. Co-infection experiments indicated that prior or concurrent infection of mosquito cells with NHUV resulted in a significant reduction in virus production of West Nile virus (WNV), St Louis encephalitis virus (SLEV) and Japanese encephalitis virus. The inhibitory effect was most effective against WNV and SLEV with over a 10(6)-fold and 10(4)-fold reduction in peak titres, respectively.


Assuntos
Culicidae/citologia , Flavivirus/genética , Flavivirus/isolamento & purificação , Sequência de Aminoácidos , Animais , Brasil , Linhagem Celular , Regulação Viral da Expressão Gênica , Dados de Sequência Molecular , Filogenia , Proteínas Virais/genética , Proteínas Virais/metabolismo , Replicação Viral
8.
Avian Dis ; 58(2): 255-61, 2014 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-25055630

RESUMO

American crows are acutely sensitive to West Nile virus (WNV) infection, and crow mortality has been used in WNV surveillance to monitor enzootic transmission. However, non-WNV sources of mortality could reduce the reliability of crow death as a surveillance tool. Here, using a combination of histopathologic, toxicologic, virologic, and molecular techniques we describe causes of mortality in 67 American crows (Corvus brachyrhynchos) that were collected from a population in the Sacramento Valley of California in 2012 and 2013. Evidence of infectious disease was detected in 70% (47/67) of carcasses. The majority of deaths were linked to a suite of non-WNV viral, bacterial, and fungal infections (39%; 23/59 cases), WNV (36%; 24/67 cases), and an acute toxic event (25%; 15/59 cases). Coinfections were detected in 20% (12/59) of birds and frequently were associated with WNV and poxviral dermatitis. Inferences about WNV activity based on crow mortality should be supported by laboratory confirmation because crow mortality frequently can be caused by other infectious diseases or toxic events.


Assuntos
Doenças das Aves/epidemiologia , Coinfecção/veterinária , Doenças Transmissíveis/veterinária , Corvos , Poluentes Ambientais/toxicidade , Monitoramento Epidemiológico , Febre do Nilo Ocidental/epidemiologia , Vírus do Nilo Ocidental/isolamento & purificação , Animais , Doenças das Aves/mortalidade , Doenças das Aves/virologia , California/epidemiologia , Cromatografia Líquida de Alta Pressão/veterinária , Cromatografia Líquida/veterinária , Coinfecção/epidemiologia , Coinfecção/mortalidade , Coinfecção/virologia , Doenças Transmissíveis/epidemiologia , Doenças Transmissíveis/etiologia , Doenças Transmissíveis/mortalidade , Monitoramento Epidemiológico/veterinária , Hepatopatias/epidemiologia , Hepatopatias/etiologia , Hepatopatias/mortalidade , Hepatopatias/veterinária , Prevalência , Reação em Cadeia da Polimerase em Tempo Real/veterinária , Reprodutibilidade dos Testes , Reação em Cadeia da Polimerase Via Transcriptase Reversa/veterinária , Estações do Ano , Sensibilidade e Especificidade , Espectrometria de Massas em Tandem/veterinária , Febre do Nilo Ocidental/mortalidade , Febre do Nilo Ocidental/virologia
9.
PLoS One ; 9(6): e100802, 2014.
Artigo em Inglês | MEDLINE | ID: mdl-24971589

RESUMO

A single helicase amino acid substitution, NS3-T249P, has been shown to increase viremia magnitude/mortality in American crows (AMCRs) following West Nile virus (WNV) infection. Lineage/intra-lineage geographic variants exhibit consistent amino acid polymorphisms at this locus; however, the majority of WNV isolates associated with recent outbreaks reported worldwide have a proline at the NS3-249 residue. In order to evaluate the impact of NS3-249 variants on avian and mammalian virulence, multiple amino acid substitutions were engineered into a WNV infectious cDNA (NY99; NS3-249P) and the resulting viruses inoculated into AMCRs, house sparrows (HOSPs) and mice. Differential viremia profiles were observed between mutant viruses in the two bird species; however, the NS3-249P virus produced the highest mean peak viral loads in both avian models. In contrast, this avian modulating virulence determinant had no effect on LD50 or the neurovirulence phenotype in the murine model. Recombinant helicase proteins demonstrated variable helicase and ATPase activities; however, differences did not correlate with avian or murine viremia phenotypes. These in vitro and in vivo data indicate that avian-specific phenotypes are modulated by critical viral-host protein interactions involving the NS3-249 residue that directly influence transmission efficiency and therefore the magnitude of WNV epizootics in nature.


Assuntos
Substituição de Aminoácidos , Especificidade de Hospedeiro , Proteínas não Estruturais Virais/genética , Vírus do Nilo Ocidental/genética , Sequência de Aminoácidos , Animais , Chlorocebus aethiops , Corvos/virologia , Camundongos , Dados de Sequência Molecular , Polimorfismo de Nucleotídeo Único , RNA Helicases/química , RNA Helicases/genética , RNA Helicases/metabolismo , Serina Endopeptidases/química , Serina Endopeptidases/genética , Serina Endopeptidases/metabolismo , Pardais/virologia , Células Vero , Proteínas não Estruturais Virais/química , Proteínas não Estruturais Virais/metabolismo , Virulência/genética , Vírus do Nilo Ocidental/patogenicidade
10.
PLoS One ; 8(7): e68988, 2013.
Artigo em Inglês | MEDLINE | ID: mdl-23894387

RESUMO

Next-generation sequencing (NGS) is emerging as a powerful tool for elucidating genetic information for a wide range of applications. Unfortunately, the surging popularity of NGS has not yet been accompanied by an improvement in automated techniques for preparing formatted sequencing libraries. To address this challenge, we have developed a prototype microfluidic system for preparing sequencer-ready DNA libraries for analysis by Illumina sequencing. Our system combines droplet-based digital microfluidic (DMF) sample handling with peripheral modules to create a fully-integrated, sample-in library-out platform. In this report, we use our automated system to prepare NGS libraries from samples of human and bacterial genomic DNA. E. coli libraries prepared on-device from 5 ng of total DNA yielded excellent sequence coverage over the entire bacterial genome, with >99% alignment to the reference genome, even genome coverage, and good quality scores. Furthermore, we produced a de novo assembly on a previously unsequenced multi-drug resistant Klebsiella pneumoniae strain BAA-2146 (KpnNDM). The new method described here is fast, robust, scalable, and automated. Our device for library preparation will assist in the integration of NGS technology into a wide variety of laboratories, including small research laboratories and clinical laboratories.


Assuntos
Biblioteca Gênica , Sequenciamento de Nucleotídeos em Larga Escala/instrumentação , Técnicas Analíticas Microfluídicas/instrumentação , Análise de Sequência de DNA/instrumentação , DNA Bacteriano/genética , Genoma Bacteriano/genética , Genoma Humano/genética , Humanos , Integração de Sistemas
11.
RNA Biol ; 10(4): 502-15, 2013 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-23558773

RESUMO

Use of second generation sequencing (SGS) technologies for transcriptional profiling (RNA-Seq) has revolutionized transcriptomics, enabling measurement of RNA abundances with unprecedented specificity and sensitivity and the discovery of novel RNA species. Preparation of RNA-Seq libraries requires conversion of the RNA starting material into cDNA flanked by platform-specific adaptor sequences. Each of the published methods and commercial kits currently available for RNA-Seq library preparation suffers from at least one major drawback, including long processing times, large starting material requirements, uneven coverage, loss of strand information and high cost. We report the development of a new RNA-Seq library preparation technique that produces representative, strand-specific RNA-Seq libraries from small amounts of starting material in a fast, simple and cost-effective manner. Additionally, we have developed a new quantitative PCR-based assay for precisely determining the number of PCR cycles to perform for optimal enrichment of the final library, a key step in all SGS library preparation workflows.


Assuntos
Escherichia coli/genética , Perfilação da Expressão Gênica/métodos , Biblioteca Gênica , Reação em Cadeia da Polimerase/métodos , Transcrição Reversa , Análise de Sequência de RNA/métodos , Sequência de Bases , Linhagem Celular Tumoral , Biologia Computacional , Sequenciamento de Nucleotídeos em Larga Escala/métodos , Humanos
12.
Anal Biochem ; 438(1): 90-6, 2013 Jul 01.
Artigo em Inglês | MEDLINE | ID: mdl-23535274

RESUMO

To fully understand the interactions of a pathogen with its host, it is necessary to analyze the RNA transcripts of both the host and pathogen throughout the course of an infection. Although this can be accomplished relatively easily on the host side, the analysis of pathogen transcripts is complicated by the overwhelming amount of host RNA isolated from an infected sample. Even with the read depth provided by second-generation sequencing, it is extremely difficult to get enough pathogen reads for an effective gene-level analysis. In this study, we describe a novel capture-based technique and device that considerably enriches for pathogen transcripts from infected samples. This versatile method can, in principle, enrich for any pathogen in any infected sample. To test the technique's efficacy, we performed time course tissue culture infections using Rift Valley fever virus and Francisella tularensis. At each time point, RNA sequencing (RNA-Seq) was performed and the results of the treated samples were compared with untreated controls. The capture of pathogen transcripts, in all cases, led to more than an order of magnitude enrichment of pathogen reads, greatly increasing the number of genes hit, the coverage of those genes, and the depth at which each transcript was sequenced.


Assuntos
Francisella tularensis/genética , Francisella tularensis/fisiologia , Interações Hospedeiro-Patógeno , Vírus da Febre do Vale do Rift/genética , Vírus da Febre do Vale do Rift/fisiologia , Análise de Sequência de RNA/métodos , Linhagem Celular , Perfilação da Expressão Gênica , Humanos , Macrófagos/microbiologia , Macrófagos/virologia , Hibridização de Ácido Nucleico , RNA Bacteriano/genética , RNA Mensageiro/genética , RNA Viral/genética
13.
Biotechniques ; 53(6): 373-80, 2012 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-23227988

RESUMO

Second-generation sequencing (SGS) has become the preferred method for RNA transcriptome profiling of organisms and single cells. However, SGS analysis of transcriptome diversity (including protein-coding transcripts and regulatory non-coding RNAs) is inefficient unless the sample of interest is first depleted of nucleic acids derived from ribosomal RNA (rRNA), which typically account for up to 95% of total intracellular RNA content. Here we describe a novel microscale hydroxyapatite chromatography (HAC) normalization method to remove eukaryotic and prokaryotic high abundant rRNA species, thereby increasing sequence coverage depth and transcript diversity across non-rRNA populations. RNA-seq analysis of Escherichia coli K-12 and human intracellular total RNA showed that HAC-based normalization enriched for all non-ribosomal RNA species regardless of RNA transcript abundance or length when compared with untreated controls. Microcolumn HAC normalization generated rRNA-depleted cDNA libraries comparable to the well-established duplex specific nuclease (DSN) normalization and Ribo-Zero rRNA-depletion methods, thus establishing microscale HAC as an effective, cost saving, and non-destructive alternative normalization technique.


Assuntos
Cromatografia de Afinidade/métodos , Durapatita/química , Biblioteca Gênica , RNA/genética , Análise de Sequência de RNA/métodos , Transcriptoma , Sequência de Bases , Cromatografia por Troca Iônica/métodos , Mapeamento Cromossômico , Escherichia coli K12/genética , Humanos , Leucócitos Mononucleares/química , RNA/análise , RNA/química
14.
Am J Trop Med Hyg ; 87(3): 559-64, 2012 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-22826479

RESUMO

To determine whether West Nile virus (WNV) persistent infection in avian hosts may potentially serve as an overwintering mechanism, House Sparrows and House Finches, experimentally and naturally infected with several strains of WNV, and two naturally infected Western Scrub-Jays were held in mosquito-proof outdoor aviaries from 2007-March 2008. Overall, 94% (n = 36) of House Sparrows, 100% (n = 14) of House Finches and 2 Western Scrub-Jays remained WNV antibody positive. When combined by species, 37% of the House Sparrows, 50% of the House Finches, and 2 Western Scrub-Jays were WNV RNA positive at necropsy, up to 36 weeks post-infection. Infectious WNV was not detected. Our study supports the hypothesis that some avian hosts support the long-term persistence of WNV RNA, but it remains unresolved whether these infections relapse to restart an avian-arthropod transmission cycle and thereby serve as an overwintering mechanism for WNV.


Assuntos
Doenças das Aves/virologia , Tentilhões/virologia , RNA Viral/isolamento & purificação , Pardais/virologia , Febre do Nilo Ocidental/veterinária , Vírus do Nilo Ocidental/isolamento & purificação , Animais , Anticorpos Antivirais/sangue , Doenças das Aves/transmissão , Culicidae/virologia , Imuno-Histoquímica , Febre do Nilo Ocidental/transmissão , Febre do Nilo Ocidental/virologia , Vírus do Nilo Ocidental/patogenicidade
15.
J Gen Virol ; 93(Pt 1): 39-49, 2012 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-21940408

RESUMO

Despite utilizing the same avian hosts and mosquito vectors, St Louis encephalitis virus (SLEV) and West Nile virus (WNV) display dissimilar vector-infectivity and vertebrate-pathogenic phenotypes. SLEV exhibits a low oral infection threshold for Culex mosquito vectors and is avirulent in avian hosts, producing low-magnitude viraemias. In contrast, WNV is less orally infective to mosquitoes and elicits high-magnitude viraemias in a wide range of avian species. In order to identify the genetic determinants of these different phenotypes and to assess the utility of mosquito and vertebrate cell lines for recapitulating in vivo differences observed between these viruses, reciprocal WNV and SLEV pre-membrane and envelope protein (prME) chimeric viruses were generated and growth of these mutant viruses was characterized in mammalian (Vero), avian (duck) and mosquito [Aedes (C6/36) and Culex (CT)] cells. In both vertebrate lines, WNV grew to 100-fold higher titres than SLEV, and growth and cytopathogenicity phenotypes, determined by chimeric phenotypes, were modulated by genetic elements outside the prME gene region. Both chimeras exhibited distinctive growth patterns from those of SLEV in C6/36 cells, indicating the role of both structural and non-structural gene regions for growth in this cell line. In contrast, growth of chimeric viruses was indistinguishable from that of virus containing homologous prME genes in CT cells, indicating that structural genetic elements could specifically dictate growth differences of these viruses in relevant vectors. These data provide genetic insight into divergent enzootic maintenance strategies that could also be useful for the assessment of emergence mechanisms of closely related flaviviruses.


Assuntos
Quimera/crescimento & desenvolvimento , Vírus da Encefalite de St. Louis/crescimento & desenvolvimento , Encefalite de St. Louis/virologia , Proteínas do Envelope Viral/metabolismo , Febre do Nilo Ocidental/virologia , Vírus do Nilo Ocidental/crescimento & desenvolvimento , Aedes , Motivos de Aminoácidos , Sequência de Aminoácidos , Animais , Linhagem Celular , Quimera/genética , Quimera/fisiologia , Culicidae , Efeito Citopatogênico Viral , Patos , Vírus da Encefalite de St. Louis/química , Vírus da Encefalite de St. Louis/genética , Vírus da Encefalite de St. Louis/fisiologia , Evolução Molecular , Humanos , Dados de Sequência Molecular , Alinhamento de Sequência , Proteínas do Envelope Viral/química , Proteínas do Envelope Viral/genética , Vírus do Nilo Ocidental/química , Vírus do Nilo Ocidental/genética , Vírus do Nilo Ocidental/fisiologia
16.
Am J Trop Med Hyg ; 85(4): 758-67, 2011 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-21976584

RESUMO

A West Nile virus (WNV) isolate from Mexico (TM171-03) and BIRD1153, a unique genotype from Texas, have exhibited reduced murine neuroinvasive phenotypes. To determine if murine neuroinvasive capacity equates to avian virulence potential, American crow (Corvus brachyrhynchos) and house sparrows (Passer domesticus) were experimentally inoculated with representative murine neuroinvasive/non-neuroinvasive strains. In both avian species, a plaque variant from Mexico that was E-glycosylation competent produced higher viremias than an E-glycosylation-incompetent variant, indicating the potential importance of E-glycosylation for avian replication. The murine non-neuroinvasive BIRD1153 strain was significantly attenuated in American crows but not house sparrows when compared with the murine neuroinvasive Texas strain. Despite the loss of murine neuroinvasive properties of nonglycosylated variants from Mexico, our data indicate avian replication potential of these strains and that unique WNV virulence characteristics exist between murine and avian models. The implications of reduced avian replication of variants from Mexico for restricted WNV transmission in Latin America is discussed.


Assuntos
Aves/virologia , Vírus do Nilo Ocidental/patogenicidade , Animais , Anticorpos Antivirais/sangue , Sequência de Bases , Primers do DNA , Glicosilação , México , Texas , Virulência , Vírus do Nilo Ocidental/imunologia , Vírus do Nilo Ocidental/isolamento & purificação
17.
J Gen Virol ; 92(Pt 12): 2810-2820, 2011 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-21865445

RESUMO

The hallmark attribute of North American West Nile virus (WNV) strains has been high pathogenicity in certain bird species. Surprisingly, this avian virulent WNV phenotype has not been observed during its geographical expansion into the Caribbean, Central America and South America. One WNV variant (TM171-03-pp1) isolated in Mexico has demonstrated an attenuated phenotype in two widely distributed North American bird species, American crows (AMCRs) and house sparrows (HOSPs). In order to identify genetic determinants associated with attenuated avian replication of the TM171-03-pp1 variant, chimeric viruses between the NY99 and Mexican strains were generated, and their replicative capacity was assessed in cell culture and in AMCR, HOSP and house finch avian hosts. The results demonstrated that mutations in both the pre-membrane (prM-I141T) and envelope (E-S156P) genes mediated the attenuation phenotype of the WNV TM171-03-pp1 variant in a chicken macrophage cell line and in all three avian species assayed. Inclusion of the prM-I141T and E-S156P TM171-03-pp1 mutations in the NY99 backbone was necessary to achieve the avian attenuation level of the Mexican virus. Furthermore, reciprocal incorporation of both prM-T141I and E-P156S substitutions into the Mexican virus genome was necessary to generate a virus that exhibited avian virulence equivalent to the NY99 virus. These structural changes may indicate the presence of new evolutionary pressures exerted on WNV populations circulating in Latin America or may signify a genetic bottleneck that has constrained their epiornitic potential in alternative geographical locations.


Assuntos
Corvos/virologia , Tentilhões/virologia , Pardais/virologia , Proteínas do Envelope Viral/metabolismo , Vírus do Nilo Ocidental/genética , Substituição de Aminoácidos , Animais , Doenças das Aves/virologia , Linhagem Celular , Galinhas , Clonagem Molecular , DNA Complementar/genética , Proteínas de Membrana/genética , México , Mutação , Fenótipo , Filogeografia , Plasmídeos/genética , Análise de Sequência de DNA , Proteínas do Envelope Viral/genética , Carga Viral , Virulência , Replicação Viral , Vírus do Nilo Ocidental/isolamento & purificação , Vírus do Nilo Ocidental/patogenicidade
18.
Nat Genet ; 39(9): 1162-6, 2007 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-17694056

RESUMO

West Nile virus (WNV), first recognized in North America in 1999, has been responsible for the largest arboviral epiornitic and epidemic of human encephalitis in recorded history. Despite the well-described epidemiological patterns of WNV in North America, the basis for the emergence of WNV-associated avian pathology, particularly in the American crow (AMCR) sentinel species, and the large scale of the North American epidemic and epiornitic is uncertain. We report here that the introduction of a T249P amino acid substitution in the NS3 helicase (found in North American WNV) in a low-virulence strain was sufficient to generate a phenotype highly virulent to AMCRs. Furthermore, comparative sequence analyses of full-length WNV genomes demonstrated that the same site (NS3-249) was subject to adaptive evolution. These phenotypic and evolutionary results provide compelling evidence for the positive selection of a mutation encoding increased viremia potential and virulence in the AMCR sentinel bird species.


Assuntos
Doenças das Aves/virologia , Corvos/virologia , Mutação , Vírus do Nilo Ocidental/genética , América , Substituição de Aminoácidos , Animais , Evolução Molecular , Genoma Viral , Geografia , Humanos , Filogenia , RNA Helicases/genética , Serina Endopeptidases/genética , Proteínas não Estruturais Virais/genética , Virulência/genética , Vírus do Nilo Ocidental/isolamento & purificação , Vírus do Nilo Ocidental/patogenicidade
19.
Avian Dis ; 51(2): 573-7, 2007 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-17626486

RESUMO

The New York 1999 strain of West Nile virus (WNV) is nearly 100% fatal in the American crow (Corvus brachyrhynchos). We evaluated four WNV vaccine formulations in American crows, including intramuscular (i.m.) DNA vaccine, i.m. DNA vaccine with adjuvant, orally administered microencapsulated DNA vaccine, and i.m. killed vaccine. Neutralizing antibodies developed in approximately 80% of crows that received the DNA vaccine i.m. (with or without adjuvant), and in 44% that received the killed vaccine. However, no crows that received the oral microencapsulated DNA vaccine or the placebo developed WNV antibodies. All crows were challenged 10 wk after initial vaccination. No unvaccinated crows survived challenge, and survival rates were 44% (i.m. DNA vaccine), 60% (i.m. DNA vaccine with adjuvant), 0% (oral microencapsulated DNA vaccine), and 11% (killed vaccine). Peak viremia titers in the birds that survived were significantly lower as compared to titers in birds that died. Parenteral administration of a WNV DNA vaccine was associated with reduced mortality but did not provide sterile immunity.


Assuntos
Doenças das Aves/prevenção & controle , Doenças das Aves/virologia , Corvos , Vacinas de DNA/imunologia , Febre do Nilo Ocidental/veterinária , Vacinas contra o Vírus do Nilo Ocidental/imunologia , Animais , Doenças das Aves/imunologia , Doenças das Aves/mortalidade , DNA Viral/imunologia , Febre do Nilo Ocidental/imunologia , Febre do Nilo Ocidental/mortalidade , Febre do Nilo Ocidental/prevenção & controle
20.
J Gen Virol ; 87(Pt 12): 3611-3622, 2006 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-17098976

RESUMO

The NY99 genotype of West Nile virus (WNV) introduced into North America has demonstrated high virulence for American crows (AMCRs), whilst a closely related WNV strain (KEN-3829) from Kenya exhibits substantially reduced virulence in AMCRs [Brault, A. C., Langevin, S. A., Bowen, R. A., Panella, N. A., Biggerstaff, B. J., Miller, B. R. & Nicholas, K. (2004). Emerg Infect Dis 10, 2161-2168]. Viruses rescued from infectious cDNA clones of both the NY99 and KEN-3829 strains demonstrated virulence comparable to that of their parental strains in AMCRs. To begin to define parameters that might explain the different virulence phenotypes between these two viruses, temperature-sensitivity assays were performed for both viruses at the high temperatures experienced in viraemic AMCRs. Growth curves of the two WNV strains were performed in African green monkey kidney (Vero; 37-42 degrees C) and duck embryonic fibroblast (DEF; 37-45 degrees C) cells cultured at temperatures that were tolerated by the cell line. Unlike the NY99 virus, marked decreases in KEN-3829 viral titres were detected between 36 and 120 h post-infection (p.i.) at temperatures above 43 degrees C. Replication of KEN-3829 viral RNA was reduced 6500-fold at 72 h p.i. in DEF cells incubated at 44 degrees C relative to levels of intracellular virus-specific RNA measured at 37 degrees C. In contrast, replication of virus derived from the NY99 infectious cDNA at 44 degrees C demonstrated only a 17-fold reduction in RNA level. These results indicated that the ability of WNV NY99 to replicate at the high temperatures measured in infected AMCRs could be an important factor leading to the increased avian virulence and emergence of this strain of WNV.


Assuntos
Doenças das Aves/virologia , Corvos/virologia , Replicação Viral , Febre do Nilo Ocidental/veterinária , Vírus do Nilo Ocidental/fisiologia , Vírus do Nilo Ocidental/patogenicidade , Animais , Temperatura Corporal , Linhagem Celular , Chlorocebus aethiops , Patos , RNA Viral/biossíntese , Análise de Sobrevida , Temperatura , Células Vero , Ensaio de Placa Viral , Virulência , Febre do Nilo Ocidental/virologia
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