Investigation of the environment and of mothers in transmission of rotavirus infections in the neonatal nursery
A distinct feature of neonatal rotavirus infection is the association of unusual strains that appear to be prevalent only in neonatal units and persist for long periods of time. The main aims of this study were to determine if rotavirus can be detected on environmental surfaces in the neonatal nurse...
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Veröffentlicht in: | Journal of medical virology 2008-06, Vol.80 (6), p.1099-1105 |
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creator | Ramani, Sasirekha Arumugam, Rajesh Gopalarathinam, Nithya Mohanty, Ipsita Mathew, Sudhin Gladstone, Beryl Primrose Jana, Atanu Kumar Kuruvilla, Kurien Anil Kang, Gagandeep |
description | A distinct feature of neonatal rotavirus infection is the association of unusual strains that appear to be prevalent only in neonatal units and persist for long periods of time. The main aims of this study were to determine if rotavirus can be detected on environmental surfaces in the neonatal nursery and whether the infection occurs in mothers of infected and uninfected neonates. Thirty rotavirus positive neonates and an equal number of negative neonates were enrolled in this study. Stool samples from 15 mothers in each group and environmental swabs collected from the bed and surfaces around neonates were tested for rotavirus using single round and nested PCR for the VP6 gene. Rotavirus could be detected in environmental swabs using single round PCR for VP6 gene in 40% of neonates positive for rotavirus antigen by enzyme immunoassay (EIA) and 33.3% of EIA negative neonates. The detection rate was almost 100% using the nested VP6 PCR. Rotavirus was detected in maternal samples only if the nested VP6 PCR was used, with no significant difference between rates of rotavirus detection in maternal fecal samples of infected and uninfected neonates (p-0.4). Sequence analysis of nested VP6 amplicons from two environmental swabs revealed them to be closest in identity to G10P[11], the most common genotype causing infections in neonates in this setting. Interestingly, sequences of amplicons from maternal stool samples did not cluster with G10P[11] or other VP6 subgroup I strains but showed clustering with human strains of VP6 subgroup II. J. Med. Virol. 80:1099-1105, 2008. |
doi_str_mv | 10.1002/jmv.21177 |
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The main aims of this study were to determine if rotavirus can be detected on environmental surfaces in the neonatal nursery and whether the infection occurs in mothers of infected and uninfected neonates. Thirty rotavirus positive neonates and an equal number of negative neonates were enrolled in this study. Stool samples from 15 mothers in each group and environmental swabs collected from the bed and surfaces around neonates were tested for rotavirus using single round and nested PCR for the VP6 gene. Rotavirus could be detected in environmental swabs using single round PCR for VP6 gene in 40% of neonates positive for rotavirus antigen by enzyme immunoassay (EIA) and 33.3% of EIA negative neonates. The detection rate was almost 100% using the nested VP6 PCR. Rotavirus was detected in maternal samples only if the nested VP6 PCR was used, with no significant difference between rates of rotavirus detection in maternal fecal samples of infected and uninfected neonates (p-0.4). Sequence analysis of nested VP6 amplicons from two environmental swabs revealed them to be closest in identity to G10P[11], the most common genotype causing infections in neonates in this setting. Interestingly, sequences of amplicons from maternal stool samples did not cluster with G10P[11] or other VP6 subgroup I strains but showed clustering with human strains of VP6 subgroup II. J. Med. Virol. 80:1099-1105, 2008.</description><identifier>ISSN: 0146-6615</identifier><identifier>EISSN: 1096-9071</identifier><identifier>DOI: 10.1002/jmv.21177</identifier><identifier>PMID: 18428133</identifier><identifier>CODEN: JMVIDB</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Antigens, Viral - analysis ; Antigens, Viral - genetics ; Beds - virology ; Biological and medical sciences ; Capsid Proteins - genetics ; Case-Control Studies ; Cross Infection - transmission ; Cross Infection - virology ; environment ; Feces - virology ; Female ; Fundamental and applied biological sciences. Psychology ; Genes, Viral - genetics ; Human viral diseases ; Humans ; Infant, Newborn ; Infant, Newborn, Diseases - virology ; Infectious diseases ; Male ; Medical sciences ; Microbiology ; Miscellaneous ; Mothers ; neonates ; Nurseries, Hospital ; nursery ; Phylogeny ; Polymerase Chain Reaction ; Rotavirus ; Rotavirus - classification ; Rotavirus - genetics ; Rotavirus - isolation & purification ; Rotavirus Infections - transmission ; Rotavirus Infections - virology ; Sensitivity and Specificity ; Viral diseases ; Virology</subject><ispartof>Journal of medical virology, 2008-06, Vol.80 (6), p.1099-1105</ispartof><rights>Copyright © 2008 Wiley‐Liss, Inc.</rights><rights>2008 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4467-2d735caca31990daa931df809555023797a938172a867b6f6fdf5c69b9eacf773</citedby><cites>FETCH-LOGICAL-c4467-2d735caca31990daa931df809555023797a938172a867b6f6fdf5c69b9eacf773</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjmv.21177$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjmv.21177$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20306306$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18428133$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ramani, Sasirekha</creatorcontrib><creatorcontrib>Arumugam, Rajesh</creatorcontrib><creatorcontrib>Gopalarathinam, Nithya</creatorcontrib><creatorcontrib>Mohanty, Ipsita</creatorcontrib><creatorcontrib>Mathew, Sudhin</creatorcontrib><creatorcontrib>Gladstone, Beryl Primrose</creatorcontrib><creatorcontrib>Jana, Atanu Kumar</creatorcontrib><creatorcontrib>Kuruvilla, Kurien Anil</creatorcontrib><creatorcontrib>Kang, Gagandeep</creatorcontrib><title>Investigation of the environment and of mothers in transmission of rotavirus infections in the neonatal nursery</title><title>Journal of medical virology</title><addtitle>J. Med. Virol</addtitle><description>A distinct feature of neonatal rotavirus infection is the association of unusual strains that appear to be prevalent only in neonatal units and persist for long periods of time. The main aims of this study were to determine if rotavirus can be detected on environmental surfaces in the neonatal nursery and whether the infection occurs in mothers of infected and uninfected neonates. Thirty rotavirus positive neonates and an equal number of negative neonates were enrolled in this study. Stool samples from 15 mothers in each group and environmental swabs collected from the bed and surfaces around neonates were tested for rotavirus using single round and nested PCR for the VP6 gene. Rotavirus could be detected in environmental swabs using single round PCR for VP6 gene in 40% of neonates positive for rotavirus antigen by enzyme immunoassay (EIA) and 33.3% of EIA negative neonates. The detection rate was almost 100% using the nested VP6 PCR. Rotavirus was detected in maternal samples only if the nested VP6 PCR was used, with no significant difference between rates of rotavirus detection in maternal fecal samples of infected and uninfected neonates (p-0.4). Sequence analysis of nested VP6 amplicons from two environmental swabs revealed them to be closest in identity to G10P[11], the most common genotype causing infections in neonates in this setting. Interestingly, sequences of amplicons from maternal stool samples did not cluster with G10P[11] or other VP6 subgroup I strains but showed clustering with human strains of VP6 subgroup II. J. Med. Virol. 80:1099-1105, 2008.</description><subject>Antigens, Viral - analysis</subject><subject>Antigens, Viral - genetics</subject><subject>Beds - virology</subject><subject>Biological and medical sciences</subject><subject>Capsid Proteins - genetics</subject><subject>Case-Control Studies</subject><subject>Cross Infection - transmission</subject><subject>Cross Infection - virology</subject><subject>environment</subject><subject>Feces - virology</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Genes, Viral - genetics</subject><subject>Human viral diseases</subject><subject>Humans</subject><subject>Infant, Newborn</subject><subject>Infant, Newborn, Diseases - virology</subject><subject>Infectious diseases</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Microbiology</subject><subject>Miscellaneous</subject><subject>Mothers</subject><subject>neonates</subject><subject>Nurseries, Hospital</subject><subject>nursery</subject><subject>Phylogeny</subject><subject>Polymerase Chain Reaction</subject><subject>Rotavirus</subject><subject>Rotavirus - classification</subject><subject>Rotavirus - genetics</subject><subject>Rotavirus - isolation & purification</subject><subject>Rotavirus Infections - transmission</subject><subject>Rotavirus Infections - virology</subject><subject>Sensitivity and Specificity</subject><subject>Viral diseases</subject><subject>Virology</subject><issn>0146-6615</issn><issn>1096-9071</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkk1v1DAQhi0EosvCgT8AuVCJQ1p_JHZ8RBVdSgsIQYGbNevYxSWxi50s7L_HIaGcEJIlSzPPvDOe1wg9JviIYEyPr_vdESVEiDtoRbDkpcSC3EUrTCpeck7qA_QgpWuMcSMpvY8OSFPRhjC2QuHM70wa3BUMLvgi2GL4agrjdy4G3xs_FODbKdyHnIipcL4YIvjUu5SWihgGyPw4Ja3Rk9DMZSVvgocBusKPMZm4f4juWeiSebTca3R5-vLjyavy4t3m7OTFRamriouStoLVGjQwIiVuASQjrW2wrOsaUyakyJGGCAoNF1tuuW1trbncSgPaCsHW6HDWvYnh-5hfqPLA2nQd5InGpLgkVYPr6r8gxVRWuJIZfD6DOoaUorHqJroe4l4RrCYbVLZB_bYhs08W0XHbm_Yvuew9A88WAJKGzuaNapduOYoZ5tNZo-OZ--E6s_93R_X6zac_rcu5wqXB_LytgPhNccFErT6_3ajN-bn8Uon3apP5pzNvISi4inmKyw8UEzZ9FiJ5zX4B2Ue4ag</recordid><startdate>200806</startdate><enddate>200806</enddate><creator>Ramani, Sasirekha</creator><creator>Arumugam, Rajesh</creator><creator>Gopalarathinam, Nithya</creator><creator>Mohanty, Ipsita</creator><creator>Mathew, Sudhin</creator><creator>Gladstone, Beryl Primrose</creator><creator>Jana, Atanu Kumar</creator><creator>Kuruvilla, Kurien Anil</creator><creator>Kang, Gagandeep</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Liss</general><scope>FBQ</scope><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7U9</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>200806</creationdate><title>Investigation of the environment and of mothers in transmission of rotavirus infections in the neonatal nursery</title><author>Ramani, Sasirekha ; Arumugam, Rajesh ; Gopalarathinam, Nithya ; Mohanty, Ipsita ; Mathew, Sudhin ; Gladstone, Beryl Primrose ; Jana, Atanu Kumar ; Kuruvilla, Kurien Anil ; Kang, Gagandeep</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4467-2d735caca31990daa931df809555023797a938172a867b6f6fdf5c69b9eacf773</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Antigens, Viral - analysis</topic><topic>Antigens, Viral - genetics</topic><topic>Beds - virology</topic><topic>Biological and medical sciences</topic><topic>Capsid Proteins - genetics</topic><topic>Case-Control Studies</topic><topic>Cross Infection - transmission</topic><topic>Cross Infection - virology</topic><topic>environment</topic><topic>Feces - virology</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Genes, Viral - genetics</topic><topic>Human viral diseases</topic><topic>Humans</topic><topic>Infant, Newborn</topic><topic>Infant, Newborn, Diseases - virology</topic><topic>Infectious diseases</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Microbiology</topic><topic>Miscellaneous</topic><topic>Mothers</topic><topic>neonates</topic><topic>Nurseries, Hospital</topic><topic>nursery</topic><topic>Phylogeny</topic><topic>Polymerase Chain Reaction</topic><topic>Rotavirus</topic><topic>Rotavirus - classification</topic><topic>Rotavirus - genetics</topic><topic>Rotavirus - isolation & purification</topic><topic>Rotavirus Infections - transmission</topic><topic>Rotavirus Infections - virology</topic><topic>Sensitivity and Specificity</topic><topic>Viral diseases</topic><topic>Virology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ramani, Sasirekha</creatorcontrib><creatorcontrib>Arumugam, Rajesh</creatorcontrib><creatorcontrib>Gopalarathinam, Nithya</creatorcontrib><creatorcontrib>Mohanty, Ipsita</creatorcontrib><creatorcontrib>Mathew, Sudhin</creatorcontrib><creatorcontrib>Gladstone, Beryl Primrose</creatorcontrib><creatorcontrib>Jana, Atanu Kumar</creatorcontrib><creatorcontrib>Kuruvilla, Kurien Anil</creatorcontrib><creatorcontrib>Kang, Gagandeep</creatorcontrib><collection>AGRIS</collection><collection>Istex</collection><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>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of medical virology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ramani, Sasirekha</au><au>Arumugam, Rajesh</au><au>Gopalarathinam, Nithya</au><au>Mohanty, Ipsita</au><au>Mathew, Sudhin</au><au>Gladstone, Beryl Primrose</au><au>Jana, Atanu Kumar</au><au>Kuruvilla, Kurien Anil</au><au>Kang, Gagandeep</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Investigation of the environment and of mothers in transmission of rotavirus infections in the neonatal nursery</atitle><jtitle>Journal of medical virology</jtitle><addtitle>J. Med. Virol</addtitle><date>2008-06</date><risdate>2008</risdate><volume>80</volume><issue>6</issue><spage>1099</spage><epage>1105</epage><pages>1099-1105</pages><issn>0146-6615</issn><eissn>1096-9071</eissn><coden>JMVIDB</coden><abstract>A distinct feature of neonatal rotavirus infection is the association of unusual strains that appear to be prevalent only in neonatal units and persist for long periods of time. The main aims of this study were to determine if rotavirus can be detected on environmental surfaces in the neonatal nursery and whether the infection occurs in mothers of infected and uninfected neonates. Thirty rotavirus positive neonates and an equal number of negative neonates were enrolled in this study. Stool samples from 15 mothers in each group and environmental swabs collected from the bed and surfaces around neonates were tested for rotavirus using single round and nested PCR for the VP6 gene. Rotavirus could be detected in environmental swabs using single round PCR for VP6 gene in 40% of neonates positive for rotavirus antigen by enzyme immunoassay (EIA) and 33.3% of EIA negative neonates. The detection rate was almost 100% using the nested VP6 PCR. Rotavirus was detected in maternal samples only if the nested VP6 PCR was used, with no significant difference between rates of rotavirus detection in maternal fecal samples of infected and uninfected neonates (p-0.4). Sequence analysis of nested VP6 amplicons from two environmental swabs revealed them to be closest in identity to G10P[11], the most common genotype causing infections in neonates in this setting. Interestingly, sequences of amplicons from maternal stool samples did not cluster with G10P[11] or other VP6 subgroup I strains but showed clustering with human strains of VP6 subgroup II. J. Med. Virol. 80:1099-1105, 2008.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>18428133</pmid><doi>10.1002/jmv.21177</doi><tpages>7</tpages></addata></record> |
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subjects | Antigens, Viral - analysis Antigens, Viral - genetics Beds - virology Biological and medical sciences Capsid Proteins - genetics Case-Control Studies Cross Infection - transmission Cross Infection - virology environment Feces - virology Female Fundamental and applied biological sciences. Psychology Genes, Viral - genetics Human viral diseases Humans Infant, Newborn Infant, Newborn, Diseases - virology Infectious diseases Male Medical sciences Microbiology Miscellaneous Mothers neonates Nurseries, Hospital nursery Phylogeny Polymerase Chain Reaction Rotavirus Rotavirus - classification Rotavirus - genetics Rotavirus - isolation & purification Rotavirus Infections - transmission Rotavirus Infections - virology Sensitivity and Specificity Viral diseases Virology |
title | Investigation of the environment and of mothers in transmission of rotavirus infections in the neonatal nursery |
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