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Complete genome sequencing and analysis of six enterovirus 71 strains with different clinical phenotypes

BACKGROUND: Hand, foot and mouth diseases (HFMD) caused by enterovirus 71(EV71) presents a broad spectrum of clinical manifestations ranging from mild febrile disease to fatal neurolocal disease. However, the mechanism of virulence is unknown. METHODS: We isolated 6 strains of EV71 from HFMD patient...

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Autores principales: Wen, Hong-ling, Si, Lu-ying, Yuan, Xiao-jing, Hao, Shu-bin, Gao, Feng, Chu, Fu-lu, Sun, Cheng-xi, Wang, Zhi-yu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3669102/
https://www.ncbi.nlm.nih.gov/pubmed/23577963
http://dx.doi.org/10.1186/1743-422X-10-115
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author Wen, Hong-ling
Si, Lu-ying
Yuan, Xiao-jing
Hao, Shu-bin
Gao, Feng
Chu, Fu-lu
Sun, Cheng-xi
Wang, Zhi-yu
author_facet Wen, Hong-ling
Si, Lu-ying
Yuan, Xiao-jing
Hao, Shu-bin
Gao, Feng
Chu, Fu-lu
Sun, Cheng-xi
Wang, Zhi-yu
author_sort Wen, Hong-ling
collection PubMed
description BACKGROUND: Hand, foot and mouth diseases (HFMD) caused by enterovirus 71(EV71) presents a broad spectrum of clinical manifestations ranging from mild febrile disease to fatal neurolocal disease. However, the mechanism of virulence is unknown. METHODS: We isolated 6 strains of EV71 from HFMD patients with or without neurological symptoms, and sequenced the whole genomes of the viruses to reveal the virulence factors of EV71. RESULTS: Phylogenetic tree based on VP1 region showed that all six strains clustered into C4a of C4 sub-genotype. In the complete polypeptide, 298 positions were found to be variable in all strains, and three of these positions (Val(P814)/Ile(P814) in VP1, Val(P1148)/Ile(P1148) in 3A and Ala (P1728)/Cys (P1728)/Val (P1728) in 3C) were conserved among the strains with neurovirulence, but variable in strains without neurovirulence. In the 5(′)-UTR region, it showed that the first 10 nucleotides were mostly conserved, however from the 11th nucleotide, nucleotide insertions and deletions were quite common. The secondary structure prediction of 5(′)-UTR sequences showed that two of three strains without neurovirulence (SDLY11 and SDLY48) were almost the same, and all strains with neurovirulence (SDLY96, SDLY107 and SDLY153) were different from each other. SDLY107 (a fatal strain) was found different from other strains on four positions (C(P241)/T(P241), A(P571)/T(P571), C(P579)/T(P579) in 5(′)-UTR and T(P7335)/C(P7335) in 3(′)-UTR). CONCLUSIONS: The three positions (Val(P814)/Ile(P814) in VP1, Val(P1148)/Ile(P1148) in 3A and Ala (P1728)/Cys (P1728)/Val (P1728) in 3C), were different between two phenotypes. These suggested that the three positions might be potential virulent positions. And the three varied positions were also found to be conserved in strains with neurovirulence, and variable in strains without neurovirulence. These might reveal that the conservation of two of the three positions or the three together were specific for the strains with neurovirulence. Varation of secondary structure of 5(′)-UTR, might be correlated to the changes of viral virulence. SDLY107 (a fatal strain) was found different from other strains on four positions, these positions might be related with death.
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spelling pubmed-36691022013-06-01 Complete genome sequencing and analysis of six enterovirus 71 strains with different clinical phenotypes Wen, Hong-ling Si, Lu-ying Yuan, Xiao-jing Hao, Shu-bin Gao, Feng Chu, Fu-lu Sun, Cheng-xi Wang, Zhi-yu Virol J Research BACKGROUND: Hand, foot and mouth diseases (HFMD) caused by enterovirus 71(EV71) presents a broad spectrum of clinical manifestations ranging from mild febrile disease to fatal neurolocal disease. However, the mechanism of virulence is unknown. METHODS: We isolated 6 strains of EV71 from HFMD patients with or without neurological symptoms, and sequenced the whole genomes of the viruses to reveal the virulence factors of EV71. RESULTS: Phylogenetic tree based on VP1 region showed that all six strains clustered into C4a of C4 sub-genotype. In the complete polypeptide, 298 positions were found to be variable in all strains, and three of these positions (Val(P814)/Ile(P814) in VP1, Val(P1148)/Ile(P1148) in 3A and Ala (P1728)/Cys (P1728)/Val (P1728) in 3C) were conserved among the strains with neurovirulence, but variable in strains without neurovirulence. In the 5(′)-UTR region, it showed that the first 10 nucleotides were mostly conserved, however from the 11th nucleotide, nucleotide insertions and deletions were quite common. The secondary structure prediction of 5(′)-UTR sequences showed that two of three strains without neurovirulence (SDLY11 and SDLY48) were almost the same, and all strains with neurovirulence (SDLY96, SDLY107 and SDLY153) were different from each other. SDLY107 (a fatal strain) was found different from other strains on four positions (C(P241)/T(P241), A(P571)/T(P571), C(P579)/T(P579) in 5(′)-UTR and T(P7335)/C(P7335) in 3(′)-UTR). CONCLUSIONS: The three positions (Val(P814)/Ile(P814) in VP1, Val(P1148)/Ile(P1148) in 3A and Ala (P1728)/Cys (P1728)/Val (P1728) in 3C), were different between two phenotypes. These suggested that the three positions might be potential virulent positions. And the three varied positions were also found to be conserved in strains with neurovirulence, and variable in strains without neurovirulence. These might reveal that the conservation of two of the three positions or the three together were specific for the strains with neurovirulence. Varation of secondary structure of 5(′)-UTR, might be correlated to the changes of viral virulence. SDLY107 (a fatal strain) was found different from other strains on four positions, these positions might be related with death. BioMed Central 2013-04-11 /pmc/articles/PMC3669102/ /pubmed/23577963 http://dx.doi.org/10.1186/1743-422X-10-115 Text en Copyright © 2013 Wen et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Wen, Hong-ling
Si, Lu-ying
Yuan, Xiao-jing
Hao, Shu-bin
Gao, Feng
Chu, Fu-lu
Sun, Cheng-xi
Wang, Zhi-yu
Complete genome sequencing and analysis of six enterovirus 71 strains with different clinical phenotypes
title Complete genome sequencing and analysis of six enterovirus 71 strains with different clinical phenotypes
title_full Complete genome sequencing and analysis of six enterovirus 71 strains with different clinical phenotypes
title_fullStr Complete genome sequencing and analysis of six enterovirus 71 strains with different clinical phenotypes
title_full_unstemmed Complete genome sequencing and analysis of six enterovirus 71 strains with different clinical phenotypes
title_short Complete genome sequencing and analysis of six enterovirus 71 strains with different clinical phenotypes
title_sort complete genome sequencing and analysis of six enterovirus 71 strains with different clinical phenotypes
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3669102/
https://www.ncbi.nlm.nih.gov/pubmed/23577963
http://dx.doi.org/10.1186/1743-422X-10-115
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