Prevalence and Diversity of Microbes in the Amniotic Fluid, the Fetal Inflammatory Response, and Pregnancy Outcome in Women with Preterm Pre-Labor Rupture of Membranes

Citation DiGiulio DB, Romero R, Kusanovic JP, Gómez R, Kim CJ, Seok K, Gotsch F, Mazaki‐Tovi S, Vaisbuch E, Sanders K, Bik EM, Chaiworapongsa T, Oyarzún E, Relman DA. Prevalence and diversity of microbes in the amniotic fluid, the fetal inflammatory response, and pregnancy outcome in women with pret...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:American journal of reproductive immunology (1989) 2010-07, Vol.64 (1), p.38-57
Hauptverfasser: DiGiulio, Daniel B., Romero, Roberto, Kusanovic, Juan Pedro, Gómez, Ricardo, Kim, Chong Jai, Seok, Kimberley S., Gotsch, Francesca, Mazaki-Tovi, Shali, Vaisbuch, Edi, Sanders, Katherine, Bik, Elisabeth M., Chaiworapongsa, Tinnakorn, Oyarzún, Enrique, Relman, David A.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 57
container_issue 1
container_start_page 38
container_title American journal of reproductive immunology (1989)
container_volume 64
creator DiGiulio, Daniel B.
Romero, Roberto
Kusanovic, Juan Pedro
Gómez, Ricardo
Kim, Chong Jai
Seok, Kimberley S.
Gotsch, Francesca
Mazaki-Tovi, Shali
Vaisbuch, Edi
Sanders, Katherine
Bik, Elisabeth M.
Chaiworapongsa, Tinnakorn
Oyarzún, Enrique
Relman, David A.
description Citation DiGiulio DB, Romero R, Kusanovic JP, Gómez R, Kim CJ, Seok K, Gotsch F, Mazaki‐Tovi S, Vaisbuch E, Sanders K, Bik EM, Chaiworapongsa T, Oyarzún E, Relman DA. Prevalence and diversity of microbes in the amniotic fluid, the fetal inflammatory response, and pregnancy outcome in women with preterm pre‐labor rupture of membranes. Am J Reprod Immunol 2010; 64: 38–57 Problem  The role played by microbial invasion of the amniotic cavity (MIAC) in preterm pre‐labor rupture of membranes (pPROM) is inadequately characterized, in part because of reliance on cultivation‐based methods. Method of study  Amniotic fluid from 204 subjects with pPROM was analyzed with both cultivation and molecular methods in a retrospective cohort study. Broad‐range and group‐specific polymerase chain reaction (PCR) assays targeted small subunit ribosomal DNA (rDNA), or other gene sequences, from bacteria, fungi, and archaea. Results were correlated with measurements of host inflammation, as well as pregnancy and perinatal outcomes. Results  The prevalence of MIAC was 34% (70/204) by culture, 45% (92/204) by PCR, and 50% (101/204) by both methods combined. The number of bacterial species revealed by PCR (44 species‐level phylotypes) was greater than that by culture (14 species) and included as‐yet uncultivated taxa. Some taxa detected by PCR have been previously associated with the gastrointestinal tract (e.g., Coprobacillus sp.), the mouth (e.g., Rothia dentocariosa), or the vagina in the setting of bacterial vaginosis (e.g., Atopobium vaginae). The relative risk for histologic chorioamnionitis was 2.1 for a positive PCR [95% confidence interval (CI), 1.4–3.0] and 2.0 for a positive culture (95% CI, 1.4–2.7). Bacterial rDNA abundance exhibited a dose relationship with gestational age at delivery (R2 = 0.26; P 
doi_str_mv 10.1111/j.1600-0897.2010.00830.x
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_744619934</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>744619934</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4020-430ffeb709d2159954da79e3c22fe4359c4717a3f15bea1b3f270444b401959e3</originalsourceid><addsrcrecordid>eNqNkcFu1DAQhiMEoqXwCsg3Ls3Wjp04lrgshW232m1RBerRcpIJ9ZI4W9tpN0_Ea9bJlr2CL2ONv_-fkf8oQgTPSDhnmxnJMI5xLvgswaGLcU7xbPcqOj48vA53zLKYM5wfRe-c2-BACcrfRkcJppSkOT-O_ny38KgaMCUgZSr0VT-CddoPqKvRWpe2K8AhbZC_BzRvje68LtGi6XV1OvUW4FWDlqZuVNsq39kB3YLbdsbB6eQYBvwyypQDuul92bUwut2FatCT9vfjuwfbjjVeqaKz6Lbf-t7CtAG0hVUG3PvoTa0aBx9e6kn0c_Htx_llvLq5WJ7PV3HJcIJjRnFdQ8GxqBKSCpGySnEBtEySGhhNRck44YrWJC1AkYLWCceMsYJhItIAnkSf9r5b2z304LxstSuhacISXe8kZywjQlD2b5LSNBMJxYHM92T4Tecs1HJrdavsIAmWY55yI8fY5BibHPOUU55yF6QfX4b0RQvVQfg3wAB83gNPuoHhv43l_GqZT6vFe7l2HnYHubK_ZcYpT-Xd9YVcX9P0y9XlWi7oM7zwvig</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>733569230</pqid></control><display><type>article</type><title>Prevalence and Diversity of Microbes in the Amniotic Fluid, the Fetal Inflammatory Response, and Pregnancy Outcome in Women with Preterm Pre-Labor Rupture of Membranes</title><source>MEDLINE</source><source>Wiley Online Library</source><creator>DiGiulio, Daniel B. ; Romero, Roberto ; Kusanovic, Juan Pedro ; Gómez, Ricardo ; Kim, Chong Jai ; Seok, Kimberley S. ; Gotsch, Francesca ; Mazaki-Tovi, Shali ; Vaisbuch, Edi ; Sanders, Katherine ; Bik, Elisabeth M. ; Chaiworapongsa, Tinnakorn ; Oyarzún, Enrique ; Relman, David A.</creator><creatorcontrib>DiGiulio, Daniel B. ; Romero, Roberto ; Kusanovic, Juan Pedro ; Gómez, Ricardo ; Kim, Chong Jai ; Seok, Kimberley S. ; Gotsch, Francesca ; Mazaki-Tovi, Shali ; Vaisbuch, Edi ; Sanders, Katherine ; Bik, Elisabeth M. ; Chaiworapongsa, Tinnakorn ; Oyarzún, Enrique ; Relman, David A.</creatorcontrib><description>Citation DiGiulio DB, Romero R, Kusanovic JP, Gómez R, Kim CJ, Seok K, Gotsch F, Mazaki‐Tovi S, Vaisbuch E, Sanders K, Bik EM, Chaiworapongsa T, Oyarzún E, Relman DA. Prevalence and diversity of microbes in the amniotic fluid, the fetal inflammatory response, and pregnancy outcome in women with preterm pre‐labor rupture of membranes. Am J Reprod Immunol 2010; 64: 38–57 Problem  The role played by microbial invasion of the amniotic cavity (MIAC) in preterm pre‐labor rupture of membranes (pPROM) is inadequately characterized, in part because of reliance on cultivation‐based methods. Method of study  Amniotic fluid from 204 subjects with pPROM was analyzed with both cultivation and molecular methods in a retrospective cohort study. Broad‐range and group‐specific polymerase chain reaction (PCR) assays targeted small subunit ribosomal DNA (rDNA), or other gene sequences, from bacteria, fungi, and archaea. Results were correlated with measurements of host inflammation, as well as pregnancy and perinatal outcomes. Results  The prevalence of MIAC was 34% (70/204) by culture, 45% (92/204) by PCR, and 50% (101/204) by both methods combined. The number of bacterial species revealed by PCR (44 species‐level phylotypes) was greater than that by culture (14 species) and included as‐yet uncultivated taxa. Some taxa detected by PCR have been previously associated with the gastrointestinal tract (e.g., Coprobacillus sp.), the mouth (e.g., Rothia dentocariosa), or the vagina in the setting of bacterial vaginosis (e.g., Atopobium vaginae). The relative risk for histologic chorioamnionitis was 2.1 for a positive PCR [95% confidence interval (CI), 1.4–3.0] and 2.0 for a positive culture (95% CI, 1.4–2.7). Bacterial rDNA abundance exhibited a dose relationship with gestational age at delivery (R2 = 0.26; P &lt; 0.01). A positive PCR was associated with lower mean birthweight, and with higher rates of respiratory distress syndrome and necrotizing enterocolitis (P &lt; 0.05 for each outcome). Conclusion  MIAC in pPROM is more common than previously recognized and is associated in some cases with uncultivated taxa, some of which are typically associated with the gastrointestinal tract. The detection of MIAC by molecular methods has clinical significance.</description><identifier>ISSN: 1046-7408</identifier><identifier>EISSN: 1600-0897</identifier><identifier>DOI: 10.1111/j.1600-0897.2010.00830.x</identifier><identifier>PMID: 20331587</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>16S ; Abundance ; Adult ; Amniotic fluid ; Amniotic Fluid - microbiology ; Archaea ; Atopobium vaginae ; Birth weight ; Cavities ; Chorioamnionitis ; Chorioamnionitis - microbiology ; cytokines ; Dopamine ; Female ; fetal inflammatory response syndrome ; Fetal Membranes, Premature Rupture - microbiology ; Fetuses ; Fungi ; Gastrointestinal tract ; Gestational age ; Humans ; Inflammation ; interleukin-6 ; intraamniotic infection ; intraamniotic inflammation ; molecular microbiology ; Mouth ; Necrotizing enterocolitis ; Nucleotide sequence ; Phylogeny ; Polymerase Chain Reaction ; Pregnancy ; Pregnancy Complications, Infectious - microbiology ; Pregnancy Outcome ; preterm birth ; preterm delivery ; preterm pre-labor rupture of membrane ; rDNA ; Respiratory distress syndrome ; Risk assessment ; Rothia dentocariosa ; Rupture ; Vagina ; Vaginosis ; Vaginosis, Bacterial - microbiology</subject><ispartof>American journal of reproductive immunology (1989), 2010-07, Vol.64 (1), p.38-57</ispartof><rights>Published 2010. This article is a US Government work and is in the public domain in the USA.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4020-430ffeb709d2159954da79e3c22fe4359c4717a3f15bea1b3f270444b401959e3</citedby><cites>FETCH-LOGICAL-c4020-430ffeb709d2159954da79e3c22fe4359c4717a3f15bea1b3f270444b401959e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1600-0897.2010.00830.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1600-0897.2010.00830.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20331587$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>DiGiulio, Daniel B.</creatorcontrib><creatorcontrib>Romero, Roberto</creatorcontrib><creatorcontrib>Kusanovic, Juan Pedro</creatorcontrib><creatorcontrib>Gómez, Ricardo</creatorcontrib><creatorcontrib>Kim, Chong Jai</creatorcontrib><creatorcontrib>Seok, Kimberley S.</creatorcontrib><creatorcontrib>Gotsch, Francesca</creatorcontrib><creatorcontrib>Mazaki-Tovi, Shali</creatorcontrib><creatorcontrib>Vaisbuch, Edi</creatorcontrib><creatorcontrib>Sanders, Katherine</creatorcontrib><creatorcontrib>Bik, Elisabeth M.</creatorcontrib><creatorcontrib>Chaiworapongsa, Tinnakorn</creatorcontrib><creatorcontrib>Oyarzún, Enrique</creatorcontrib><creatorcontrib>Relman, David A.</creatorcontrib><title>Prevalence and Diversity of Microbes in the Amniotic Fluid, the Fetal Inflammatory Response, and Pregnancy Outcome in Women with Preterm Pre-Labor Rupture of Membranes</title><title>American journal of reproductive immunology (1989)</title><addtitle>Am J Reprod Immunol</addtitle><description>Citation DiGiulio DB, Romero R, Kusanovic JP, Gómez R, Kim CJ, Seok K, Gotsch F, Mazaki‐Tovi S, Vaisbuch E, Sanders K, Bik EM, Chaiworapongsa T, Oyarzún E, Relman DA. Prevalence and diversity of microbes in the amniotic fluid, the fetal inflammatory response, and pregnancy outcome in women with preterm pre‐labor rupture of membranes. Am J Reprod Immunol 2010; 64: 38–57 Problem  The role played by microbial invasion of the amniotic cavity (MIAC) in preterm pre‐labor rupture of membranes (pPROM) is inadequately characterized, in part because of reliance on cultivation‐based methods. Method of study  Amniotic fluid from 204 subjects with pPROM was analyzed with both cultivation and molecular methods in a retrospective cohort study. Broad‐range and group‐specific polymerase chain reaction (PCR) assays targeted small subunit ribosomal DNA (rDNA), or other gene sequences, from bacteria, fungi, and archaea. Results were correlated with measurements of host inflammation, as well as pregnancy and perinatal outcomes. Results  The prevalence of MIAC was 34% (70/204) by culture, 45% (92/204) by PCR, and 50% (101/204) by both methods combined. The number of bacterial species revealed by PCR (44 species‐level phylotypes) was greater than that by culture (14 species) and included as‐yet uncultivated taxa. Some taxa detected by PCR have been previously associated with the gastrointestinal tract (e.g., Coprobacillus sp.), the mouth (e.g., Rothia dentocariosa), or the vagina in the setting of bacterial vaginosis (e.g., Atopobium vaginae). The relative risk for histologic chorioamnionitis was 2.1 for a positive PCR [95% confidence interval (CI), 1.4–3.0] and 2.0 for a positive culture (95% CI, 1.4–2.7). Bacterial rDNA abundance exhibited a dose relationship with gestational age at delivery (R2 = 0.26; P &lt; 0.01). A positive PCR was associated with lower mean birthweight, and with higher rates of respiratory distress syndrome and necrotizing enterocolitis (P &lt; 0.05 for each outcome). Conclusion  MIAC in pPROM is more common than previously recognized and is associated in some cases with uncultivated taxa, some of which are typically associated with the gastrointestinal tract. The detection of MIAC by molecular methods has clinical significance.</description><subject>16S</subject><subject>Abundance</subject><subject>Adult</subject><subject>Amniotic fluid</subject><subject>Amniotic Fluid - microbiology</subject><subject>Archaea</subject><subject>Atopobium vaginae</subject><subject>Birth weight</subject><subject>Cavities</subject><subject>Chorioamnionitis</subject><subject>Chorioamnionitis - microbiology</subject><subject>cytokines</subject><subject>Dopamine</subject><subject>Female</subject><subject>fetal inflammatory response syndrome</subject><subject>Fetal Membranes, Premature Rupture - microbiology</subject><subject>Fetuses</subject><subject>Fungi</subject><subject>Gastrointestinal tract</subject><subject>Gestational age</subject><subject>Humans</subject><subject>Inflammation</subject><subject>interleukin-6</subject><subject>intraamniotic infection</subject><subject>intraamniotic inflammation</subject><subject>molecular microbiology</subject><subject>Mouth</subject><subject>Necrotizing enterocolitis</subject><subject>Nucleotide sequence</subject><subject>Phylogeny</subject><subject>Polymerase Chain Reaction</subject><subject>Pregnancy</subject><subject>Pregnancy Complications, Infectious - microbiology</subject><subject>Pregnancy Outcome</subject><subject>preterm birth</subject><subject>preterm delivery</subject><subject>preterm pre-labor rupture of membrane</subject><subject>rDNA</subject><subject>Respiratory distress syndrome</subject><subject>Risk assessment</subject><subject>Rothia dentocariosa</subject><subject>Rupture</subject><subject>Vagina</subject><subject>Vaginosis</subject><subject>Vaginosis, Bacterial - microbiology</subject><issn>1046-7408</issn><issn>1600-0897</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkcFu1DAQhiMEoqXwCsg3Ls3Wjp04lrgshW232m1RBerRcpIJ9ZI4W9tpN0_Ea9bJlr2CL2ONv_-fkf8oQgTPSDhnmxnJMI5xLvgswaGLcU7xbPcqOj48vA53zLKYM5wfRe-c2-BACcrfRkcJppSkOT-O_ny38KgaMCUgZSr0VT-CddoPqKvRWpe2K8AhbZC_BzRvje68LtGi6XV1OvUW4FWDlqZuVNsq39kB3YLbdsbB6eQYBvwyypQDuul92bUwut2FatCT9vfjuwfbjjVeqaKz6Lbf-t7CtAG0hVUG3PvoTa0aBx9e6kn0c_Htx_llvLq5WJ7PV3HJcIJjRnFdQ8GxqBKSCpGySnEBtEySGhhNRck44YrWJC1AkYLWCceMsYJhItIAnkSf9r5b2z304LxstSuhacISXe8kZywjQlD2b5LSNBMJxYHM92T4Tecs1HJrdavsIAmWY55yI8fY5BibHPOUU55yF6QfX4b0RQvVQfg3wAB83gNPuoHhv43l_GqZT6vFe7l2HnYHubK_ZcYpT-Xd9YVcX9P0y9XlWi7oM7zwvig</recordid><startdate>201007</startdate><enddate>201007</enddate><creator>DiGiulio, Daniel B.</creator><creator>Romero, Roberto</creator><creator>Kusanovic, Juan Pedro</creator><creator>Gómez, Ricardo</creator><creator>Kim, Chong Jai</creator><creator>Seok, Kimberley S.</creator><creator>Gotsch, Francesca</creator><creator>Mazaki-Tovi, Shali</creator><creator>Vaisbuch, Edi</creator><creator>Sanders, Katherine</creator><creator>Bik, Elisabeth M.</creator><creator>Chaiworapongsa, Tinnakorn</creator><creator>Oyarzún, Enrique</creator><creator>Relman, David A.</creator><general>Blackwell Publishing Ltd</general><scope>BSCLL</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>7X8</scope><scope>7T5</scope><scope>7T7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope></search><sort><creationdate>201007</creationdate><title>Prevalence and Diversity of Microbes in the Amniotic Fluid, the Fetal Inflammatory Response, and Pregnancy Outcome in Women with Preterm Pre-Labor Rupture of Membranes</title><author>DiGiulio, Daniel B. ; Romero, Roberto ; Kusanovic, Juan Pedro ; Gómez, Ricardo ; Kim, Chong Jai ; Seok, Kimberley S. ; Gotsch, Francesca ; Mazaki-Tovi, Shali ; Vaisbuch, Edi ; Sanders, Katherine ; Bik, Elisabeth M. ; Chaiworapongsa, Tinnakorn ; Oyarzún, Enrique ; Relman, David A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4020-430ffeb709d2159954da79e3c22fe4359c4717a3f15bea1b3f270444b401959e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>16S</topic><topic>Abundance</topic><topic>Adult</topic><topic>Amniotic fluid</topic><topic>Amniotic Fluid - microbiology</topic><topic>Archaea</topic><topic>Atopobium vaginae</topic><topic>Birth weight</topic><topic>Cavities</topic><topic>Chorioamnionitis</topic><topic>Chorioamnionitis - microbiology</topic><topic>cytokines</topic><topic>Dopamine</topic><topic>Female</topic><topic>fetal inflammatory response syndrome</topic><topic>Fetal Membranes, Premature Rupture - microbiology</topic><topic>Fetuses</topic><topic>Fungi</topic><topic>Gastrointestinal tract</topic><topic>Gestational age</topic><topic>Humans</topic><topic>Inflammation</topic><topic>interleukin-6</topic><topic>intraamniotic infection</topic><topic>intraamniotic inflammation</topic><topic>molecular microbiology</topic><topic>Mouth</topic><topic>Necrotizing enterocolitis</topic><topic>Nucleotide sequence</topic><topic>Phylogeny</topic><topic>Polymerase Chain Reaction</topic><topic>Pregnancy</topic><topic>Pregnancy Complications, Infectious - microbiology</topic><topic>Pregnancy Outcome</topic><topic>preterm birth</topic><topic>preterm delivery</topic><topic>preterm pre-labor rupture of membrane</topic><topic>rDNA</topic><topic>Respiratory distress syndrome</topic><topic>Risk assessment</topic><topic>Rothia dentocariosa</topic><topic>Rupture</topic><topic>Vagina</topic><topic>Vaginosis</topic><topic>Vaginosis, Bacterial - microbiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>DiGiulio, Daniel B.</creatorcontrib><creatorcontrib>Romero, Roberto</creatorcontrib><creatorcontrib>Kusanovic, Juan Pedro</creatorcontrib><creatorcontrib>Gómez, Ricardo</creatorcontrib><creatorcontrib>Kim, Chong Jai</creatorcontrib><creatorcontrib>Seok, Kimberley S.</creatorcontrib><creatorcontrib>Gotsch, Francesca</creatorcontrib><creatorcontrib>Mazaki-Tovi, Shali</creatorcontrib><creatorcontrib>Vaisbuch, Edi</creatorcontrib><creatorcontrib>Sanders, Katherine</creatorcontrib><creatorcontrib>Bik, Elisabeth M.</creatorcontrib><creatorcontrib>Chaiworapongsa, Tinnakorn</creatorcontrib><creatorcontrib>Oyarzún, Enrique</creatorcontrib><creatorcontrib>Relman, David A.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Immunology Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>American journal of reproductive immunology (1989)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>DiGiulio, Daniel B.</au><au>Romero, Roberto</au><au>Kusanovic, Juan Pedro</au><au>Gómez, Ricardo</au><au>Kim, Chong Jai</au><au>Seok, Kimberley S.</au><au>Gotsch, Francesca</au><au>Mazaki-Tovi, Shali</au><au>Vaisbuch, Edi</au><au>Sanders, Katherine</au><au>Bik, Elisabeth M.</au><au>Chaiworapongsa, Tinnakorn</au><au>Oyarzún, Enrique</au><au>Relman, David A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Prevalence and Diversity of Microbes in the Amniotic Fluid, the Fetal Inflammatory Response, and Pregnancy Outcome in Women with Preterm Pre-Labor Rupture of Membranes</atitle><jtitle>American journal of reproductive immunology (1989)</jtitle><addtitle>Am J Reprod Immunol</addtitle><date>2010-07</date><risdate>2010</risdate><volume>64</volume><issue>1</issue><spage>38</spage><epage>57</epage><pages>38-57</pages><issn>1046-7408</issn><eissn>1600-0897</eissn><abstract>Citation DiGiulio DB, Romero R, Kusanovic JP, Gómez R, Kim CJ, Seok K, Gotsch F, Mazaki‐Tovi S, Vaisbuch E, Sanders K, Bik EM, Chaiworapongsa T, Oyarzún E, Relman DA. Prevalence and diversity of microbes in the amniotic fluid, the fetal inflammatory response, and pregnancy outcome in women with preterm pre‐labor rupture of membranes. Am J Reprod Immunol 2010; 64: 38–57 Problem  The role played by microbial invasion of the amniotic cavity (MIAC) in preterm pre‐labor rupture of membranes (pPROM) is inadequately characterized, in part because of reliance on cultivation‐based methods. Method of study  Amniotic fluid from 204 subjects with pPROM was analyzed with both cultivation and molecular methods in a retrospective cohort study. Broad‐range and group‐specific polymerase chain reaction (PCR) assays targeted small subunit ribosomal DNA (rDNA), or other gene sequences, from bacteria, fungi, and archaea. Results were correlated with measurements of host inflammation, as well as pregnancy and perinatal outcomes. Results  The prevalence of MIAC was 34% (70/204) by culture, 45% (92/204) by PCR, and 50% (101/204) by both methods combined. The number of bacterial species revealed by PCR (44 species‐level phylotypes) was greater than that by culture (14 species) and included as‐yet uncultivated taxa. Some taxa detected by PCR have been previously associated with the gastrointestinal tract (e.g., Coprobacillus sp.), the mouth (e.g., Rothia dentocariosa), or the vagina in the setting of bacterial vaginosis (e.g., Atopobium vaginae). The relative risk for histologic chorioamnionitis was 2.1 for a positive PCR [95% confidence interval (CI), 1.4–3.0] and 2.0 for a positive culture (95% CI, 1.4–2.7). Bacterial rDNA abundance exhibited a dose relationship with gestational age at delivery (R2 = 0.26; P &lt; 0.01). A positive PCR was associated with lower mean birthweight, and with higher rates of respiratory distress syndrome and necrotizing enterocolitis (P &lt; 0.05 for each outcome). Conclusion  MIAC in pPROM is more common than previously recognized and is associated in some cases with uncultivated taxa, some of which are typically associated with the gastrointestinal tract. The detection of MIAC by molecular methods has clinical significance.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>20331587</pmid><doi>10.1111/j.1600-0897.2010.00830.x</doi><tpages>20</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1046-7408
ispartof American journal of reproductive immunology (1989), 2010-07, Vol.64 (1), p.38-57
issn 1046-7408
1600-0897
language eng
recordid cdi_proquest_miscellaneous_744619934
source MEDLINE; Wiley Online Library
subjects 16S
Abundance
Adult
Amniotic fluid
Amniotic Fluid - microbiology
Archaea
Atopobium vaginae
Birth weight
Cavities
Chorioamnionitis
Chorioamnionitis - microbiology
cytokines
Dopamine
Female
fetal inflammatory response syndrome
Fetal Membranes, Premature Rupture - microbiology
Fetuses
Fungi
Gastrointestinal tract
Gestational age
Humans
Inflammation
interleukin-6
intraamniotic infection
intraamniotic inflammation
molecular microbiology
Mouth
Necrotizing enterocolitis
Nucleotide sequence
Phylogeny
Polymerase Chain Reaction
Pregnancy
Pregnancy Complications, Infectious - microbiology
Pregnancy Outcome
preterm birth
preterm delivery
preterm pre-labor rupture of membrane
rDNA
Respiratory distress syndrome
Risk assessment
Rothia dentocariosa
Rupture
Vagina
Vaginosis
Vaginosis, Bacterial - microbiology
title Prevalence and Diversity of Microbes in the Amniotic Fluid, the Fetal Inflammatory Response, and Pregnancy Outcome in Women with Preterm Pre-Labor Rupture of Membranes
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-04T15%3A24%3A03IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Prevalence%20and%20Diversity%20of%20Microbes%20in%20the%20Amniotic%20Fluid,%20the%20Fetal%20Inflammatory%20Response,%20and%20Pregnancy%20Outcome%20in%20Women%20with%20Preterm%20Pre-Labor%20Rupture%20of%20Membranes&rft.jtitle=American%20journal%20of%20reproductive%20immunology%20(1989)&rft.au=DiGiulio,%20Daniel%20B.&rft.date=2010-07&rft.volume=64&rft.issue=1&rft.spage=38&rft.epage=57&rft.pages=38-57&rft.issn=1046-7408&rft.eissn=1600-0897&rft_id=info:doi/10.1111/j.1600-0897.2010.00830.x&rft_dat=%3Cproquest_cross%3E744619934%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=733569230&rft_id=info:pmid/20331587&rfr_iscdi=true