Bacterial infiltration in structural heart valve disease
The pathology of structural valvular heart disease (sVHD) ranges from basic diseases of rheumatologic origin to chronic degenerative remodeling processes after acute bacterial infections. Molecular genetic methods allow detection of the complete microbial spectrum in heart valve tissues independent...
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Veröffentlicht in: | The Journal of thoracic and cardiovascular surgery 2020-01, Vol.159 (1), p.116-124.e4 |
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creator | Oberbach, Andreas Friedrich, Maik Lehmann, Stefanie Schlichting, Nadine Kullnick, Yvonne Gräber, Sandra Buschmann, Tilo Hagl, Christian Bagaev, Erik Gruhle, Miriam Albert, Marion Luehr, Maximilian Pichlmaier, Maximilian Rodloff, Arne C. Reiche, Kristin Kraft, Theresa Horn, Friedemann |
description | The pathology of structural valvular heart disease (sVHD) ranges from basic diseases of rheumatologic origin to chronic degenerative remodeling processes after acute bacterial infections. Molecular genetic methods allow detection of the complete microbial spectrum in heart valve tissues independent of microbiological cultivation. In particular, whole-metagenome analysis is a sensitive and highly specific analytical method that allows a deeper insight into the pathogenicity of the diseases. In the present study we assessed the pathogen spectrum in heart valve tissue from 25 sVHD patients using molecular and microbiological methods.
Twenty-five sVHD patients were selected randomly from an observational cohort study (March 2016 to January 2017). The explanted native heart valves were examined using microbiological methods and immunohistological structural analysis. In addition, the bacterial metagenome of the heart valve tissue was determined using next-generation sequencing.
The use of sonication as a pretreatment of valve tissue from 4 sVHD patients permitted successful detection of Clostridium difficile, Enterococcus faecalis, Staphylococcus saccharolyticus, and Staphylococcus haemolyticus using microbial cultivation. Histological staining revealed intramural localization. Metagenome analysis identified a higher rate of bacterial infiltration in 52% of cases. The pathogen spectrum included both gram-positive and gram-negative bacteria.
Microbiological and molecular biological studies are necessary to detect the spectrum of bacteria in a calcified heart valve. Metagenome analysis is a valid method to gain new insight into the polymicrobial pathophysiology of sVHD. Our results suggest that an undetected proportion of sVHD might be triggered by chronic inflammation or influenced by secondary bacterial infiltration. |
doi_str_mv | 10.1016/j.jtcvs.2019.02.019 |
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Twenty-five sVHD patients were selected randomly from an observational cohort study (March 2016 to January 2017). The explanted native heart valves were examined using microbiological methods and immunohistological structural analysis. In addition, the bacterial metagenome of the heart valve tissue was determined using next-generation sequencing.
The use of sonication as a pretreatment of valve tissue from 4 sVHD patients permitted successful detection of Clostridium difficile, Enterococcus faecalis, Staphylococcus saccharolyticus, and Staphylococcus haemolyticus using microbial cultivation. Histological staining revealed intramural localization. Metagenome analysis identified a higher rate of bacterial infiltration in 52% of cases. The pathogen spectrum included both gram-positive and gram-negative bacteria.
Microbiological and molecular biological studies are necessary to detect the spectrum of bacteria in a calcified heart valve. Metagenome analysis is a valid method to gain new insight into the polymicrobial pathophysiology of sVHD. Our results suggest that an undetected proportion of sVHD might be triggered by chronic inflammation or influenced by secondary bacterial infiltration.</description><identifier>ISSN: 0022-5223</identifier><identifier>EISSN: 1097-685X</identifier><identifier>DOI: 10.1016/j.jtcvs.2019.02.019</identifier><identifier>PMID: 30885626</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>bacterial infiltration ; calcification ; metagenome analysis ; polymicrobial ; structural valvular heart disease ; transcatheter aortic valve implantation</subject><ispartof>The Journal of thoracic and cardiovascular surgery, 2020-01, Vol.159 (1), p.116-124.e4</ispartof><rights>2019 The American Association for Thoracic Surgery</rights><rights>Copyright © 2019 The American Association for Thoracic Surgery. Published by Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c359t-6bd6136e401bcb1152a0ebfe1e032b45b7adc5173aaadeecf1e76db3ac6510993</citedby><cites>FETCH-LOGICAL-c359t-6bd6136e401bcb1152a0ebfe1e032b45b7adc5173aaadeecf1e76db3ac6510993</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.jtcvs.2019.02.019$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30885626$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Oberbach, Andreas</creatorcontrib><creatorcontrib>Friedrich, Maik</creatorcontrib><creatorcontrib>Lehmann, Stefanie</creatorcontrib><creatorcontrib>Schlichting, Nadine</creatorcontrib><creatorcontrib>Kullnick, Yvonne</creatorcontrib><creatorcontrib>Gräber, Sandra</creatorcontrib><creatorcontrib>Buschmann, Tilo</creatorcontrib><creatorcontrib>Hagl, Christian</creatorcontrib><creatorcontrib>Bagaev, Erik</creatorcontrib><creatorcontrib>Gruhle, Miriam</creatorcontrib><creatorcontrib>Albert, Marion</creatorcontrib><creatorcontrib>Luehr, Maximilian</creatorcontrib><creatorcontrib>Pichlmaier, Maximilian</creatorcontrib><creatorcontrib>Rodloff, Arne C.</creatorcontrib><creatorcontrib>Reiche, Kristin</creatorcontrib><creatorcontrib>Kraft, Theresa</creatorcontrib><creatorcontrib>Horn, Friedemann</creatorcontrib><creatorcontrib>Bioinformatics group</creatorcontrib><creatorcontrib>Clinical Microbiology group</creatorcontrib><creatorcontrib>CardiOmics group</creatorcontrib><title>Bacterial infiltration in structural heart valve disease</title><title>The Journal of thoracic and cardiovascular surgery</title><addtitle>J Thorac Cardiovasc Surg</addtitle><description>The pathology of structural valvular heart disease (sVHD) ranges from basic diseases of rheumatologic origin to chronic degenerative remodeling processes after acute bacterial infections. Molecular genetic methods allow detection of the complete microbial spectrum in heart valve tissues independent of microbiological cultivation. In particular, whole-metagenome analysis is a sensitive and highly specific analytical method that allows a deeper insight into the pathogenicity of the diseases. In the present study we assessed the pathogen spectrum in heart valve tissue from 25 sVHD patients using molecular and microbiological methods.
Twenty-five sVHD patients were selected randomly from an observational cohort study (March 2016 to January 2017). The explanted native heart valves were examined using microbiological methods and immunohistological structural analysis. In addition, the bacterial metagenome of the heart valve tissue was determined using next-generation sequencing.
The use of sonication as a pretreatment of valve tissue from 4 sVHD patients permitted successful detection of Clostridium difficile, Enterococcus faecalis, Staphylococcus saccharolyticus, and Staphylococcus haemolyticus using microbial cultivation. Histological staining revealed intramural localization. Metagenome analysis identified a higher rate of bacterial infiltration in 52% of cases. The pathogen spectrum included both gram-positive and gram-negative bacteria.
Microbiological and molecular biological studies are necessary to detect the spectrum of bacteria in a calcified heart valve. Metagenome analysis is a valid method to gain new insight into the polymicrobial pathophysiology of sVHD. Our results suggest that an undetected proportion of sVHD might be triggered by chronic inflammation or influenced by secondary bacterial infiltration.</description><subject>bacterial infiltration</subject><subject>calcification</subject><subject>metagenome analysis</subject><subject>polymicrobial</subject><subject>structural valvular heart disease</subject><subject>transcatheter aortic valve implantation</subject><issn>0022-5223</issn><issn>1097-685X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp9kE9LxDAQxYMo7rr6CQTp0UvrJGnS7cGDLv6DBS8K3kKaTjGl22qSFvz2Zt3Vo6fHML83w3uEnFPIKFB51WZtMJPPGNAyA5ZFOSBzCmWRyqV4OyRzAMZSwRifkRPvWwAoInRMZhyWSyGZnJPlrTYBndVdYvvGdsHpYIc-DokPbjRhdHH1jtqFZNLdhEltPWqPp-So0Z3Hs70uyOv93cvqMV0_Pzytbtap4aIMqaxqSbnEHGhlKkoF04BVgxSBsyoXVaFrI2jBtdY1omkoFrKuuDZSxCglX5DL3d0PN3yO6IPaWG-w63SPw-gVo2VOeQE5RJTvUOMG7x026sPZjXZfioLaVqZa9VOZ2lamgKko0XWxfzBWG6z_PL8dReB6B2CMOVl0yhuLvcHaOjRB1YP998E39Vd-1g</recordid><startdate>202001</startdate><enddate>202001</enddate><creator>Oberbach, Andreas</creator><creator>Friedrich, Maik</creator><creator>Lehmann, Stefanie</creator><creator>Schlichting, Nadine</creator><creator>Kullnick, Yvonne</creator><creator>Gräber, Sandra</creator><creator>Buschmann, Tilo</creator><creator>Hagl, Christian</creator><creator>Bagaev, Erik</creator><creator>Gruhle, Miriam</creator><creator>Albert, Marion</creator><creator>Luehr, Maximilian</creator><creator>Pichlmaier, Maximilian</creator><creator>Rodloff, Arne C.</creator><creator>Reiche, Kristin</creator><creator>Kraft, Theresa</creator><creator>Horn, Friedemann</creator><general>Elsevier Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>202001</creationdate><title>Bacterial infiltration in structural heart valve disease</title><author>Oberbach, Andreas ; Friedrich, Maik ; Lehmann, Stefanie ; Schlichting, Nadine ; Kullnick, Yvonne ; Gräber, Sandra ; Buschmann, Tilo ; Hagl, Christian ; Bagaev, Erik ; Gruhle, Miriam ; Albert, Marion ; Luehr, Maximilian ; Pichlmaier, Maximilian ; Rodloff, Arne C. ; Reiche, Kristin ; Kraft, Theresa ; Horn, Friedemann</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c359t-6bd6136e401bcb1152a0ebfe1e032b45b7adc5173aaadeecf1e76db3ac6510993</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>bacterial infiltration</topic><topic>calcification</topic><topic>metagenome analysis</topic><topic>polymicrobial</topic><topic>structural valvular heart disease</topic><topic>transcatheter aortic valve implantation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Oberbach, Andreas</creatorcontrib><creatorcontrib>Friedrich, Maik</creatorcontrib><creatorcontrib>Lehmann, Stefanie</creatorcontrib><creatorcontrib>Schlichting, Nadine</creatorcontrib><creatorcontrib>Kullnick, Yvonne</creatorcontrib><creatorcontrib>Gräber, Sandra</creatorcontrib><creatorcontrib>Buschmann, Tilo</creatorcontrib><creatorcontrib>Hagl, Christian</creatorcontrib><creatorcontrib>Bagaev, Erik</creatorcontrib><creatorcontrib>Gruhle, Miriam</creatorcontrib><creatorcontrib>Albert, Marion</creatorcontrib><creatorcontrib>Luehr, Maximilian</creatorcontrib><creatorcontrib>Pichlmaier, Maximilian</creatorcontrib><creatorcontrib>Rodloff, Arne C.</creatorcontrib><creatorcontrib>Reiche, Kristin</creatorcontrib><creatorcontrib>Kraft, Theresa</creatorcontrib><creatorcontrib>Horn, Friedemann</creatorcontrib><creatorcontrib>Bioinformatics group</creatorcontrib><creatorcontrib>Clinical Microbiology group</creatorcontrib><creatorcontrib>CardiOmics group</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of thoracic and cardiovascular surgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Oberbach, Andreas</au><au>Friedrich, Maik</au><au>Lehmann, Stefanie</au><au>Schlichting, Nadine</au><au>Kullnick, Yvonne</au><au>Gräber, Sandra</au><au>Buschmann, Tilo</au><au>Hagl, Christian</au><au>Bagaev, Erik</au><au>Gruhle, Miriam</au><au>Albert, Marion</au><au>Luehr, Maximilian</au><au>Pichlmaier, Maximilian</au><au>Rodloff, Arne C.</au><au>Reiche, Kristin</au><au>Kraft, Theresa</au><au>Horn, Friedemann</au><aucorp>Bioinformatics group</aucorp><aucorp>Clinical Microbiology group</aucorp><aucorp>CardiOmics group</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Bacterial infiltration in structural heart valve disease</atitle><jtitle>The Journal of thoracic and cardiovascular surgery</jtitle><addtitle>J Thorac Cardiovasc Surg</addtitle><date>2020-01</date><risdate>2020</risdate><volume>159</volume><issue>1</issue><spage>116</spage><epage>124.e4</epage><pages>116-124.e4</pages><issn>0022-5223</issn><eissn>1097-685X</eissn><abstract>The pathology of structural valvular heart disease (sVHD) ranges from basic diseases of rheumatologic origin to chronic degenerative remodeling processes after acute bacterial infections. Molecular genetic methods allow detection of the complete microbial spectrum in heart valve tissues independent of microbiological cultivation. In particular, whole-metagenome analysis is a sensitive and highly specific analytical method that allows a deeper insight into the pathogenicity of the diseases. In the present study we assessed the pathogen spectrum in heart valve tissue from 25 sVHD patients using molecular and microbiological methods.
Twenty-five sVHD patients were selected randomly from an observational cohort study (March 2016 to January 2017). The explanted native heart valves were examined using microbiological methods and immunohistological structural analysis. In addition, the bacterial metagenome of the heart valve tissue was determined using next-generation sequencing.
The use of sonication as a pretreatment of valve tissue from 4 sVHD patients permitted successful detection of Clostridium difficile, Enterococcus faecalis, Staphylococcus saccharolyticus, and Staphylococcus haemolyticus using microbial cultivation. Histological staining revealed intramural localization. Metagenome analysis identified a higher rate of bacterial infiltration in 52% of cases. The pathogen spectrum included both gram-positive and gram-negative bacteria.
Microbiological and molecular biological studies are necessary to detect the spectrum of bacteria in a calcified heart valve. Metagenome analysis is a valid method to gain new insight into the polymicrobial pathophysiology of sVHD. Our results suggest that an undetected proportion of sVHD might be triggered by chronic inflammation or influenced by secondary bacterial infiltration.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>30885626</pmid><doi>10.1016/j.jtcvs.2019.02.019</doi></addata></record> |
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subjects | bacterial infiltration calcification metagenome analysis polymicrobial structural valvular heart disease transcatheter aortic valve implantation |
title | Bacterial infiltration in structural heart valve disease |
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