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1.
J Med Virol ; 91(1): 155-160, 2019 01.
Artículo en Inglés | MEDLINE | ID: mdl-30168582

RESUMEN

Coxsackievirus A16 (CV-A16) commonly causes mild symptoms, but severe diseases, such as aseptic meningitis, encephalitis, and even fatal cases, have been reported. Thirteen CV-A16 strains were isolated from patients with severe hand, foot, and mouth disease in Yunnan, Southwest China, from 2009 to 2015. Subgenotype B1a and B1b of CV-A16 were predominantly circulating the region with B1b the predominant strain in recent years. The mean rate of nucleotide substitution based on the VP1 gene sequence was 4.545 × 10 -3 substitution per site per year from 2009 to 2015. These results may help in understanding the genetic diversity of CV-A16 and develop a CV-A16 vaccine.


Asunto(s)
Enterovirus/clasificación , Enterovirus/aislamiento & purificación , Genotipo , Enfermedad de Boca, Mano y Pie/patología , Enfermedad de Boca, Mano y Pie/virología , Niño , Preescolar , China/epidemiología , Enterovirus/genética , Enfermedad de Boca, Mano y Pie/epidemiología , Humanos , Tasa de Mutación , Proteínas Estructurales Virales/genética
2.
J Med Virol ; 91(5): 881-885, 2019 05.
Artículo en Inglés | MEDLINE | ID: mdl-30613995

RESUMEN

Hand, foot, and mouth disease (HFMD) is a common infectious disease caused by enteroviruses (EVs). In this study, a total of 341 children with serious HFMD were admitted to a pediatric hospital in Yunnan, China in 2012 to 2016. EVs were detected in 283 specimens (83.0%) and were assigned to 17 EV types. Enterovirus A71 (EV-A71) was predominant, accounting for 41.6%, and was followed by coxsackievirus A16 (CV-A16; 18.8%), CV-A6 (9.1%), CV-A10 and E-9 (2.9%), CV-B5 (1.8%), CV-A9 (1.2%), E-30 (0.9%), E-18, CV-A4, C-B3, and CV-A2 (0.6%) and other EV types such as CV-A8, CV-A14, E-14, E-11, and CV-B4 (0.3%). All of the EV-A71 isolates belonged to C4a; the CV-A16 belonged to B1b or B1a, although the B1b strains were predominant; and CV-A6 belonged to D3. In 2012 to 2014, E-9 was the third most frequent serotype (8.2%, 5.0%, and 6.5%, respectively). E-9 was not detected in 2015 and 2016. CV-A6 was not detected in 2012 but was the second most frequent serotype (25.3%) in 2015. Active etiological surveillance of HFMD makes it necessary to be aware of these emerging pathogens.


Asunto(s)
Enterovirus/clasificación , Enterovirus/aislamiento & purificación , Enfermedad de Boca, Mano y Pie/epidemiología , Enfermedad de Boca, Mano y Pie/etiología , Serogrupo , Preescolar , China/epidemiología , Femenino , Enfermedad de Boca, Mano y Pie/patología , Hospitales , Humanos , Masculino
3.
Virol J ; 16(1): 63, 2019 05 08.
Artículo en Inglés | MEDLINE | ID: mdl-31068194

RESUMEN

BACKGROUND: Hand, foot, and mouth disease (HFMD) is a common childhood disease, which is usually caused by enterovirus A (EV-A) serotypes. Enterovirus A71 (EV-A71) and coxsackievirus A16 (CV-A16) are the main etiologic agents. Multiple serotypes of enterovirus B serotypes (EV-B) have been detected in outbreaks or sporadic cases of HFMD. RESULTS: During HFMD surveillance in Yunnan, China in 2013, two echovirus 33 (E-33) isolates were recovered in cell culture and typed by molecular methods from the cerebrospinal fluid (CSF) and feces of two sporadic cases of HFMD complicated by meningitis. Sequence analysis indicated that the study isolates, YNK35 and YNA12, formed an independent branch, and belonged to E-33 genotype H. Recombination analysis indicated multiple recombination events in the genomic sequence of isolate YNK35. The recombination mainly occurred in the non-structural coding region of P2 and P3, and involved intra-species recombination of species B. CONCLUSION: In this study, the complete sequences of two E-33 isolates were determined. This is the first report of severe HFMD associated with E-33 in Yunnan China, and it enriches the number of full-length genome sequences of E-33 in the GenBank database.


Asunto(s)
Enterovirus Humano B/genética , Enfermedad de Boca, Mano y Pie/complicaciones , Enfermedad de Boca, Mano y Pie/virología , Meningitis/virología , Recombinación Genética , China/epidemiología , Enterovirus Humano B/aislamiento & purificación , Monitoreo Epidemiológico , Femenino , Variación Genética , Genoma Viral , Enfermedad de Boca, Mano y Pie/líquido cefalorraquídeo , Humanos , Lactante , Masculino , Filogenia , Serogrupo , Secuenciación Completa del Genoma
4.
Arch Virol ; 162(1): 307-311, 2017 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-27709402

RESUMEN

Human coxsackievirus B2 (CVB2) belongs to the species Human enterovirus B and can cause aseptic meningitis, myocarditis and hand-foot-mouth disease (HFMD). We first determined the complete genome of the RW41-2/YN/CHN/2012 strain, isolated from a patient with HFMD and aseptic meningitis in the Yunnan Province, China in 2012. The strain shared 83.5 % and 82.2 % nucleotide similarity with CVB2 prototype strain Ohio-1, in the complete VP1 gene and the complete genome, respectively. Using phylogenetic and homogeneity analyses for the complete VP1 gene, CVB2 strains could be divided into four genogroups (A-D); the RW41-2/YN/CHN/2012 strain belonging to genogroup D. The amino acid sequence of VP1 is highly conserved. Recombination analyses showed the newly isolated RW41-2/YN/CHN/2012 strain was probably a recombinant, which was closely related to strain CVB2 (KM386639) in the genomic P1 and P2 regions and strains of other human enterovirus B (HEV-B) viruses (KT353721, JX644073, and KP262053) in the P3 region.


Asunto(s)
Enterovirus Humano B/clasificación , Enterovirus Humano B/aislamiento & purificación , Genoma Viral , Enfermedad de Boca, Mano y Pie/virología , ARN Viral/genética , Análisis de Secuencia de ADN , Preescolar , China , Análisis por Conglomerados , Enterovirus Humano B/genética , Genotipo , Enfermedad de Boca, Mano y Pie/complicaciones , Humanos , Masculino , Meningitis Aséptica/virología , Filogenia , Recombinación Genética , Homología de Secuencia de Ácido Nucleico
5.
Medicine (Baltimore) ; 97(31): e11610, 2018 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-30075535

RESUMEN

Hand, foot, and mouth disease (HFMD) is a common infectious disease caused by multiple enteroviruses (EVs) in China. To better define the etiologic agents and clinical characteristics of HFMD, we conducted this study in Yunnan, China.In this study, 1280 stool specimens were collected from pediatric patients hospitalized for treatment of HFMD in 2010. EV was detected with nested reverse transcription polymerase chain reaction and directly genotyped by gene sequencing of the viral protein 1 (VP1) region. Phylogenetic analysis was performed based on the VP1 partial gene and the clinical characteristics were analyzed using SPSS Software.Of 1280 specimens, 1115 (87.1%) tested positive for EV. Seventeen different EV serotypes were detected. Coxsackievirus A16 (CA16) was the most frequently detected serotype (615/1115 cases, 55.1%), followed by enterovirus 71 (EV71; 392/1115, 35.2%), CA10 (45/1115, 4.0%), and CA4 (23/1115, 2.1%). Among the 709 severe cases, CA16, EV71, CA10, and CA4 accounted for 48.0%, 42.0%, 3.5%, and 2.3%, respectively. Of the 26 critical cases, 13 were caused by EV71, 9 by CA16, 2 by CA4, and 1 each were the result of CA10 and E9, respectively. All EV71, CA16, CA10, and CA4 isolates were highly homologous to the strains isolated from mainland China, and belonged to the C4a, B1a, G, and C genotypes, respectively.Our study showed that EV71 and CA16 were the main causative agents for severe and critical HFMD, but other serotypes can also cause severe and critical cases.


Asunto(s)
Enterovirus/genética , Heces/virología , Enfermedad de Boca, Mano y Pie/virología , Adolescente , Niño , Preescolar , China/epidemiología , Brotes de Enfermedades , Femenino , Genotipo , Enfermedad de Boca, Mano y Pie/epidemiología , Hospitalización , Humanos , Lactante , Masculino , Filogenia , Serogrupo
6.
Sci Rep ; 7(1): 8448, 2017 08 16.
Artículo en Inglés | MEDLINE | ID: mdl-28814774

RESUMEN

Human echovirus 18 (E-18) is a member of the enterovirus B species. To date, sixteen full-length genome sequences of E-18 are available in the GenBank database. In this study, we describe the complete genomic characterization of two E-18 strains isolated in Yunnan, China. Pairwise comparisons of the nucleotide sequences and the deduced amino acid sequences revealed that the two Yunnan E-18 strains had 87.5% nucleotide identity and 96.3-96.5% amino acid identity with the Chinese strain. Phylogenetic and bootscanning analyses revealed the two E-18 strains had the highest identity with other several EV-B serotypes than the other E-18 strains in the P3 coding region, especially, 3B region of the Swine Vesicular disease virus (SVDV) strain HK70, indicated that frequent intertypic recombination might have occurred in the two Yunnan strains. This study contributes the complete genome sequences of E-18 to the GenBank database and provides valuable information on the molecular epidemiology of E-18 in China.


Asunto(s)
Enterovirus Humano B/genética , Enterovirus Humano B/fisiología , Enfermedad de Boca, Mano y Pie/virología , Recombinación Genética , Células A549 , Línea Celular , Línea Celular Tumoral , Enterovirus Humano B/clasificación , Genoma Viral/genética , Genómica/métodos , Humanos , Filogenia , Análisis de Secuencia de ADN , Especificidad de la Especie
7.
Genome Announc ; 5(19)2017 May 11.
Artículo en Inglés | MEDLINE | ID: mdl-28495768

RESUMEN

The complete genome sequence of the enterovirus 71 strain CSF15/YN/CHN/2013, first isolated from cerebrospinal fluid of a child in Yunnan, China, in 2013, was determined. According to the phylogenetic and homogeneity analyses, the isolate was assigned to subgenotype C4a.

8.
Genome Announc ; 5(23)2017 Jun 08.
Artículo en Inglés | MEDLINE | ID: mdl-28596404

RESUMEN

Human echovirus 20 (E-20) belongs to the Human enterovirus B (HEV-B) species and is often detected in nonpolio enterovirus cases of acute flaccid paralysis. We determined the complete genome of strain 812/YN/CHN/2010, isolated from a child with severe hand-foot-and-mouth disease in Yunnan, China, in 2010.

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