Characterization of sapoviruses detected in gastroenteritis outbreaks and identification of asymptomatic adults with high viral load

Abstract Background Sapovirus (SaV) is a pathogen of acute gastroenteritis, and contains a positive-sense single-stranded 7.5 kb RNA genome. Characterization of SaV has been mainly performed with short nucleotide sequences, and the viral load has not been widely determined. Objectives To characteriz...

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Veröffentlicht in:Journal of clinical virology 2009-05, Vol.45 (1), p.67-71
Hauptverfasser: Yoshida, Tetsuya, Kasuo, Shizuko, Azegami, Yuka, Uchiyama, Yurie, Satsumabayashi, Kazuyo, Shiraishi, Takashi, Katayama, Kazuhiko, Wakita, Takaji, Takeda, Naokazu, Oka, Tomoichiro
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container_issue 1
container_start_page 67
container_title Journal of clinical virology
container_volume 45
creator Yoshida, Tetsuya
Kasuo, Shizuko
Azegami, Yuka
Uchiyama, Yurie
Satsumabayashi, Kazuyo
Shiraishi, Takashi
Katayama, Kazuhiko
Wakita, Takaji
Takeda, Naokazu
Oka, Tomoichiro
description Abstract Background Sapovirus (SaV) is a pathogen of acute gastroenteritis, and contains a positive-sense single-stranded 7.5 kb RNA genome. Characterization of SaV has been mainly performed with short nucleotide sequences, and the viral load has not been widely determined. Objectives To characterize SaV strains from two outbreaks in Nagano Prefecture, Japan, using long nucleotide sequences and to measure the viral load in feces. Study design Approximately 2.3 kb of the 3′ terminus of the genome corresponding to the entire capsid gene, ORF2 gene, and 3′ untranslated region were amplified with semi-nested RT-PCR followed by sequencing analysis. The copy numbers of the SaV genome were determined with real-time RT-PCR. Results In Outbreak 1, SaV strains belonging to genogroup I (GI) were detected from seven symptomatic nursery children, in which six SaV isolates had identical nucleotide sequences while one had a single synonymous nucleotide substitution. In Outbreak 2, two similar GIV SaV sequences were detected, in which three nucleotide differences accompanying two non-synonymous substitutions were observed between symptomatic high school students and asymptomatic food handlers at a hotel. The cDNA copies were 1.36 × 107 to 1.05 × 1011 ( n = 7), and 5.05 × 106 to 1.27 × 1010 ( n = 6) per gram of stool specimens in the two outbreaks. Conclusions The nucleotide sequence covering the 3′ terminal 2.3 kb of the genome is useful for better characterization of the SaV strains. In addition, we found for the first time adults who secreted SaV with high viral loads without gastroenteritis symptoms.
doi_str_mv 10.1016/j.jcv.2009.03.003
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Characterization of SaV has been mainly performed with short nucleotide sequences, and the viral load has not been widely determined. Objectives To characterize SaV strains from two outbreaks in Nagano Prefecture, Japan, using long nucleotide sequences and to measure the viral load in feces. Study design Approximately 2.3 kb of the 3′ terminus of the genome corresponding to the entire capsid gene, ORF2 gene, and 3′ untranslated region were amplified with semi-nested RT-PCR followed by sequencing analysis. The copy numbers of the SaV genome were determined with real-time RT-PCR. Results In Outbreak 1, SaV strains belonging to genogroup I (GI) were detected from seven symptomatic nursery children, in which six SaV isolates had identical nucleotide sequences while one had a single synonymous nucleotide substitution. In Outbreak 2, two similar GIV SaV sequences were detected, in which three nucleotide differences accompanying two non-synonymous substitutions were observed between symptomatic high school students and asymptomatic food handlers at a hotel. The cDNA copies were 1.36 × 107 to 1.05 × 1011 ( n = 7), and 5.05 × 106 to 1.27 × 1010 ( n = 6) per gram of stool specimens in the two outbreaks. Conclusions The nucleotide sequence covering the 3′ terminal 2.3 kb of the genome is useful for better characterization of the SaV strains. In addition, we found for the first time adults who secreted SaV with high viral loads without gastroenteritis symptoms.</description><identifier>ISSN: 1386-6532</identifier><identifier>EISSN: 1873-5967</identifier><identifier>DOI: 10.1016/j.jcv.2009.03.003</identifier><identifier>PMID: 19369115</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Adolescent ; Adult ; Allergy and Immunology ; Asymptomatic infection ; Biological and medical sciences ; Caliciviridae Infections - epidemiology ; Caliciviridae Infections - virology ; Carrier State - virology ; Child, Preschool ; Direct sequencing ; Disease Outbreaks ; Feces - virology ; Female ; Food Handling ; Fundamental and applied biological sciences. 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Characterization of SaV has been mainly performed with short nucleotide sequences, and the viral load has not been widely determined. Objectives To characterize SaV strains from two outbreaks in Nagano Prefecture, Japan, using long nucleotide sequences and to measure the viral load in feces. Study design Approximately 2.3 kb of the 3′ terminus of the genome corresponding to the entire capsid gene, ORF2 gene, and 3′ untranslated region were amplified with semi-nested RT-PCR followed by sequencing analysis. The copy numbers of the SaV genome were determined with real-time RT-PCR. Results In Outbreak 1, SaV strains belonging to genogroup I (GI) were detected from seven symptomatic nursery children, in which six SaV isolates had identical nucleotide sequences while one had a single synonymous nucleotide substitution. In Outbreak 2, two similar GIV SaV sequences were detected, in which three nucleotide differences accompanying two non-synonymous substitutions were observed between symptomatic high school students and asymptomatic food handlers at a hotel. The cDNA copies were 1.36 × 107 to 1.05 × 1011 ( n = 7), and 5.05 × 106 to 1.27 × 1010 ( n = 6) per gram of stool specimens in the two outbreaks. Conclusions The nucleotide sequence covering the 3′ terminal 2.3 kb of the genome is useful for better characterization of the SaV strains. 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Psychology</topic><topic>Gastroenteritis - epidemiology</topic><topic>Gastroenteritis - virology</topic><topic>Genome, Viral</topic><topic>Human viral diseases</topic><topic>Humans</topic><topic>Infectious Disease</topic><topic>Infectious diseases</topic><topic>Japan</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Microbiology</topic><topic>Miscellaneous</topic><topic>Nested RT-PCR</topic><topic>Outbreak</topic><topic>Phylogeny</topic><topic>Real-time RT-PCR</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>RNA, Viral - genetics</topic><topic>Sapovirus</topic><topic>Sapovirus - classification</topic><topic>Sapovirus - genetics</topic><topic>Sapovirus - isolation &amp; purification</topic><topic>Schools</topic><topic>Schools, Nursery</topic><topic>Viral diseases</topic><topic>Viral Load</topic><topic>Virology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yoshida, Tetsuya</creatorcontrib><creatorcontrib>Kasuo, Shizuko</creatorcontrib><creatorcontrib>Azegami, Yuka</creatorcontrib><creatorcontrib>Uchiyama, Yurie</creatorcontrib><creatorcontrib>Satsumabayashi, Kazuyo</creatorcontrib><creatorcontrib>Shiraishi, Takashi</creatorcontrib><creatorcontrib>Katayama, Kazuhiko</creatorcontrib><creatorcontrib>Wakita, Takaji</creatorcontrib><creatorcontrib>Takeda, Naokazu</creatorcontrib><creatorcontrib>Oka, Tomoichiro</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of clinical virology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yoshida, Tetsuya</au><au>Kasuo, Shizuko</au><au>Azegami, Yuka</au><au>Uchiyama, Yurie</au><au>Satsumabayashi, Kazuyo</au><au>Shiraishi, Takashi</au><au>Katayama, Kazuhiko</au><au>Wakita, Takaji</au><au>Takeda, Naokazu</au><au>Oka, Tomoichiro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Characterization of sapoviruses detected in gastroenteritis outbreaks and identification of asymptomatic adults with high viral load</atitle><jtitle>Journal of clinical virology</jtitle><addtitle>J Clin Virol</addtitle><date>2009-05-01</date><risdate>2009</risdate><volume>45</volume><issue>1</issue><spage>67</spage><epage>71</epage><pages>67-71</pages><issn>1386-6532</issn><eissn>1873-5967</eissn><abstract>Abstract Background Sapovirus (SaV) is a pathogen of acute gastroenteritis, and contains a positive-sense single-stranded 7.5 kb RNA genome. Characterization of SaV has been mainly performed with short nucleotide sequences, and the viral load has not been widely determined. Objectives To characterize SaV strains from two outbreaks in Nagano Prefecture, Japan, using long nucleotide sequences and to measure the viral load in feces. Study design Approximately 2.3 kb of the 3′ terminus of the genome corresponding to the entire capsid gene, ORF2 gene, and 3′ untranslated region were amplified with semi-nested RT-PCR followed by sequencing analysis. The copy numbers of the SaV genome were determined with real-time RT-PCR. Results In Outbreak 1, SaV strains belonging to genogroup I (GI) were detected from seven symptomatic nursery children, in which six SaV isolates had identical nucleotide sequences while one had a single synonymous nucleotide substitution. In Outbreak 2, two similar GIV SaV sequences were detected, in which three nucleotide differences accompanying two non-synonymous substitutions were observed between symptomatic high school students and asymptomatic food handlers at a hotel. The cDNA copies were 1.36 × 107 to 1.05 × 1011 ( n = 7), and 5.05 × 106 to 1.27 × 1010 ( n = 6) per gram of stool specimens in the two outbreaks. Conclusions The nucleotide sequence covering the 3′ terminal 2.3 kb of the genome is useful for better characterization of the SaV strains. In addition, we found for the first time adults who secreted SaV with high viral loads without gastroenteritis symptoms.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>19369115</pmid><doi>10.1016/j.jcv.2009.03.003</doi><tpages>5</tpages></addata></record>
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subjects Adolescent
Adult
Allergy and Immunology
Asymptomatic infection
Biological and medical sciences
Caliciviridae Infections - epidemiology
Caliciviridae Infections - virology
Carrier State - virology
Child, Preschool
Direct sequencing
Disease Outbreaks
Feces - virology
Female
Food Handling
Fundamental and applied biological sciences. Psychology
Gastroenteritis - epidemiology
Gastroenteritis - virology
Genome, Viral
Human viral diseases
Humans
Infectious Disease
Infectious diseases
Japan
Male
Medical sciences
Microbiology
Miscellaneous
Nested RT-PCR
Outbreak
Phylogeny
Real-time RT-PCR
Reverse Transcriptase Polymerase Chain Reaction
RNA, Viral - genetics
Sapovirus
Sapovirus - classification
Sapovirus - genetics
Sapovirus - isolation & purification
Schools
Schools, Nursery
Viral diseases
Viral Load
Virology
title Characterization of sapoviruses detected in gastroenteritis outbreaks and identification of asymptomatic adults with high viral load
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