Infective EndocarditisMeta-ENDONCT03199287
Clinical Metagenomics of Infective Endocarditis
An observational study of Infective Endocarditis, run by University Hospital, Geneva at 1 site in Switzerland.
Trial summary
Infective endocarditis (IE) is an infection of cardiac valves. IE mainly involves bacteria, more rarely fungi. IE is an uncommon diseases with an estimated incidence of 1-12 cases per 100,000 inhabitants per year. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Infective Endocarditis
- How many people
- 20 participants
- Where
- 1 siteSwitzerland
- Study dates
- 8 Jun 2017to 30 Mar 2021
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- Adult, Older adult
Study population: Adult patient undergoing valvular surgery in the context of suspicion of IE.
Who may be able to join
- The criteria for inclusion of patients are:
- Age over 18 years-old
- Patient operated for valvular surgery in a context of suspected IE.
- Collection of per-operative samples sent to the central bacteriological laboratory for the purpose of establishing a microbiological diagnosis.
- Obtaining the consent of the patient.
Who cannot join
- The exclusion criteria are:
- Opposition of the patient to participate in the study.
- Insufficient quantity (<500 μL) of sampling to perform conventional analyzes and DNA extraction in this project (may be a secondary exclusion criterion if the patient has already given consent).
Trial locations and contacts
1 site in 1 country.
About this study
Infective endocarditis (IE) is an infection of cardiac valves. IE mainly involves bacteria, more rarely fungi. IE is an uncommon diseases with an estimated incidence of 1-12 cases per 100,000 inhabitants per year. The diagnostic of IE relies on the culture of biological samples (blood cultures and per-operative samples) in the bacteriology laboratory in order to identify the pathogen and its susceptibility to antimicrobials. Nonetheless in about 10% of the cases, the blood cultures remain negative, due to antibiotics taken before harvesting, to non-culturable bacteria or to aseptic phenomena.
Clinical metagenomics is defined as the application of high-throughput sequencing (NGS) followed by a specific bioinformatics analysis to obtain clinical information, i.e. pathogen identification and the prediction of their susceptibility to antimicrobials. The metagenome of a sample (i.e. all the genomes of the organisms present) virtually contains all the information necessary for bacteriological diagnosis: what is the pathogenic bacteria , and to which antibiotics it is susceptible.
Hence, using clinical metagenomics in the context of IE appears seducing in order to overcome the limitations of conventional methods based on culture. Here, we propose to assess the performance of clinical metagenomics in the diagnostic of IE.
Read the detailed description
Background and Rationale Infective endocarditis (IE) is an infection of cardiac valves. IE mainly involves bacteria, more rarely fungi. IE is an uncommon diseases with an estimated incidence of 1-12 cases per 100,000 inhabitants per year. The diagnostic of IE relies on the collection of biological samples (blood cultures and per-operative samples) and their culture in the bacteriology laboratory, referred to as conventional methods.
This process, practically unchanged since the time of Pasteur at the end of the 19th century, has the disadvantage of allowing the only detection of the bacteria that can be grown under the usual conditions of a laboratory. If most pathogenic bacteria can do so, some bacteria that may be involved in IE (eg Coxiella sp., Bartonella sp., Tropheryma whipplei) require very specific conditions to multiply. In addition, the prior intake of antibiotics by the patient before the sample collection may negatively influence the culture of the samples. The diagnosis of IE is evoked by considering a range of clinical arguments (fever, microbiological risk behavior (positive blood culture(s), serology (for Coxiella burnettii), echography (presence of an intra-cardiac mass, abscess, leakage and / or disinsertion of a valve), all of which are minor and major criteria for determining the certainty of IE. The treatment of IE is based on prolonged antibiotics (4 to 6 weeks for the majority of cases) and valvular surgery (according to precise indications).
In about 10% of the cases, however, the blood cultures remain negative. These are known as negative culture IE, which may be due to antibiotics taken before sampling, to non-culturable bacteria or to aseptic phenomena. The broad-range PCR which consists of amplifying by PCR then sequencing a fraction of the 16S RNA encoding gene can then be used. It allows the identification of the pathogenic bacterium, but does not give information on any resistance acquired to antibiotics.
Concept of clinical metagenomics Clinical metagenomics is defined as the application of high-throughput sequencing (NGS) followed by a specific bioinformatics analysis to obtain clinical information, i.e. pathogen identification and the prediction of their susceptibility to antimicrobials. The metagenome of a sample (i.e. all the genomes of the organisms present) virtually contains all the information necessary for bacteriological diagnosis: what is / are the pathogenic bacteria (s), and to which antibiotics it/they is/are susceptible. The concept of clinical metagenomics has developed in parallel with the new DNA sequencing technologies introduced in the mid-2000s and much more efficient in terms of throughput than the sequencing method described by Sanger. While this concept is attractive, there are still many obstacles to its implementation. First, clinical specimens from bacterial infections usually contain a high concentration of leukocytes, the genome of which is about 1000 times larger than that of bacteria. Thus, the first limiting step for clinical metagenomics is the need to obtain sufficient bacterial DNA to allow the preparation of quality libraries for sequencing, but also to reduce the concentration of human DNA whose sequencing is unnecessary in this context . Methods are available but their evaluation for clinical metagenomics purposes is necessary. Secondly, the complexity of the bioinformatics data to be managed by a microbiologist requires that data be exploited as automated as possible together with a user-friendly interface, which is not the case today even if online platforms are being developed. The taxonomic assignment of sequences, their assembly, the identification of genes and chromosomal mutations associated with antibiotic resistance, and the establishment of a link between the resistance determinant and the host bacterium are additional obstacles to the implementation of clinical metagenomics. Finally, if the time taken to obtain results that can be exploited by the microbiologist tends to decrease, it is now comparable to that of culture, at a much higher cost. However, sustained competition between sequencer manufacturers should maintain their decline as has been the case over the last decade.
Relevance of the use of clinical metagenomics in IE
The use of clinical metagenomics in the context of IE therefore seems relevant for several reasons:
- Most IE are monomicrobial, which support the good performance of clinical metagenomics according to our preliminary results.
- The culture of intraoperative samples performed in an IE context is sometimes negative, due to antibiotic pre-treatment and / or non-cultivation under the routine conditions of the pathogen (eg Bartonella spp or Coxiella spp.), leaving room for improvement.
- The treatment of IE is a long-term treatment that requires accurate diagnosis in accordance with pathogens' susceptibility to antibiotics. If the pathogen is not found in culture, broad spectrum antibiotics should be administered to the patient with a double risk of treatment failure and toxicity. However, clinical metagenomics could provide information on antibiotic sensitivity even in the case of a negative culture.
- In most cases, the microbiological diagnosis of IE is not an emergency diagnosis, which is compatible with the use of clinical metagenomics for which the time of implementation is at best 48-72h.
Hence, we propose to assess the performance of clinical metagenomics in the diagnostic of IE.
- Conditions
- Infective Endocarditis
- Keywords
- metagenomics, next-generation sequencing, bioinformatics, antibiotic susceptibility
- Medical subject headings
- Endocarditis
What is being measured
The primary outcome is the main question the study is designed to answer.
Diagnostic of IE
The diagnostic of IE obtained by conventional methods and by clinical metagenomics
Measured: 24 months
Secondary outcomes (3)
Number of species identified by conventional methods but not by clinical metagenomics
Number of species identified by conventional methods but not by clinical metagenomics
Measured: 24 months
Number of species not identified by conventional methods but found in clinical metagenomics
Number of species not identified by conventional methods but found in clinical metagenomics
Measured: 24 months
Inference of antibiotic susceptibility
For each antibiotic, number of patients for whom prediction of bacterial sensitivity agrees with the sensitivity data obtained by conventional methods.
Measured: 24 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted26 Jun 2017
- Study start8 Jun 2017
- Primary completion31 Dec 2020
- Study completion30 Mar 2021
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Infective EndocarditisStudies of the same condition, open and under way.
- More trials run by University Hospital, GenevaThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 20 participants (actual)
Sponsor and investigators
- Lead sponsor
- University Hospital, Geneva
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Prof. Jacques SCHRENZEL, University Hospital, Geneva
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT03199287
- Sponsor's protocol ID
- 2017-00114
- Other IDs
- 2017
- Acronym
- Meta-ENDO
- Status last verified
- Apr 2021
- First submitted
- 22 Jun 2017
- Last updated
- 28 Apr 2021
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 28 Apr 2021. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Clinical Metagenomics of Infective Endocarditis
- ClinicalTrials.gov ID
- NCT03199287
- Acronym / sponsor ID
- Meta-ENDO / 2017-00114
- Conditions
- Infective Endocarditis
- Keywords
- metagenomics, next-generation sequencing, bioinformatics, antibiotic susceptibility
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 20 participants (actual)
- Lead sponsor
- University Hospital, GenevaUniversity, hospital or other
- Study start
- 8 Jun 2017 (actual)
- Primary completion
- 31 Dec 2020 (actual)
- Study completion
- 30 Mar 2021 (actual)
- First posted
- 26 Jun 2017 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Infective endocarditis (IE) is an infection of cardiac valves. IE mainly involves bacteria, more rarely fungi. IE is an uncommon diseases with an estimated incidence of 1-12 cases per 100,000 inhabitants per year. The diagnostic of IE relies on the culture of biological samples (blood cultures and per-operative samples) in the bacteriology laboratory in order to identify the pathogen and its susceptibility to antimicrobials. Nonetheless in about 10% of the cases, the blood cultures remain negative, due to antibiotics taken before harvesting, to non-culturable bacteria or to aseptic phenomena.
Clinical metagenomics is defined as the application of high-throughput sequencing (NGS) followed by a specific bioinformatics analysis to obtain clinical information, i.e. pathogen identification and the prediction of their susceptibility to antimicrobials. The metagenome of a sample (i.e. all the genomes of the organisms present) virtually contains all the information necessary for bacteriological diagnosis: what is the pathogenic bacteria , and to which antibiotics it is susceptible.
Hence, using clinical metagenomics in the context of IE appears seducing in order to overcome the limitations of conventional methods based on culture. Here, we propose to assess the performance of clinical metagenomics in the diagnostic of IE.
Detailed description
Background and Rationale Infective endocarditis (IE) is an infection of cardiac valves. IE mainly involves bacteria, more rarely fungi. IE is an uncommon diseases with an estimated incidence of 1-12 cases per 100,000 inhabitants per year. The diagnostic of IE relies on the collection of biological samples (blood cultures and per-operative samples) and their culture in the bacteriology laboratory, referred to as conventional methods.
This process, practically unchanged since the time of Pasteur at the end of the 19th century, has the disadvantage of allowing the only detection of the bacteria that can be grown under the usual conditions of a laboratory. If most pathogenic bacteria can do so, some bacteria that may be involved in IE (eg Coxiella sp., Bartonella sp., Tropheryma whipplei) require very specific conditions to multiply. In addition, the prior intake of antibiotics by the patient before the sample collection may negatively influence the culture of the samples. The diagnosis of IE is evoked by considering a range of clinical arguments (fever, microbiological risk behavior (positive blood culture(s), serology (for Coxiella burnettii), echography (presence of an intra-cardiac mass, abscess, leakage and / or disinsertion of a valve), all of which are minor and major criteria for determining the certainty of IE. The treatment of IE is based on prolonged antibiotics (4 to 6 weeks for the majority of cases) and valvular surgery (according to precise indications).
In about 10% of the cases, however, the blood cultures remain negative. These are known as negative culture IE, which may be due to antibiotics taken before sampling, to non-culturable bacteria or to aseptic phenomena. The broad-range PCR which consists of amplifying by PCR then sequencing a fraction of the 16S RNA encoding gene can then be used. It allows the identification of the pathogenic bacterium, but does not give information on any resistance acquired to antibiotics.
Concept of clinical metagenomics Clinical metagenomics is defined as the application of high-throughput sequencing (NGS) followed by a specific bioinformatics analysis to obtain clinical information, i.e. pathogen identification and the prediction of their susceptibility to antimicrobials. The metagenome of a sample (i.e. all the genomes of the organisms present) virtually contains all the information necessary for bacteriological diagnosis: what is / are the pathogenic bacteria (s), and to which antibiotics it/they is/are susceptible. The concept of clinical metagenomics has developed in parallel with the new DNA sequencing technologies introduced in the mid-2000s and much more efficient in terms of throughput than the sequencing method described by Sanger. While this concept is attractive, there are still many obstacles to its implementation. First, clinical specimens from bacterial infections usually contain a high concentration of leukocytes, the genome of which is about 1000 times larger than that of bacteria. Thus, the first limiting step for clinical metagenomics is the need to obtain sufficient bacterial DNA to allow the preparation of quality libraries for sequencing, but also to reduce the concentration of human DNA whose sequencing is unnecessary in this context . Methods are available but their evaluation for clinical metagenomics purposes is necessary. Secondly, the complexity of the bioinformatics data to be managed by a microbiologist requires that data be exploited as automated as possible together with a user-friendly interface, which is not the case today even if online platforms are being developed. The taxonomic assignment of sequences, their assembly, the identification of genes and chromosomal mutations associated with antibiotic resistance, and the establishment of a link between the resistance determinant and the host bacterium are additional obstacles to the implementation of clinical metagenomics. Finally, if the time taken to obtain results that can be exploited by the microbiologist tends to decrease, it is now comparable to that of culture, at a much higher cost. However, sustained competition between sequencer manufacturers should maintain their decline as has been the case over the last decade.
Relevance of the use of clinical metagenomics in IE
The use of clinical metagenomics in the context of IE therefore seems relevant for several reasons:
- Most IE are monomicrobial, which support the good performance of clinical metagenomics according to our preliminary results.
- The culture of intraoperative samples performed in an IE context is sometimes negative, due to antibiotic pre-treatment and / or non-cultivation under the routine conditions of the pathogen (eg Bartonella spp or Coxiella spp.), leaving room for improvement.
- The treatment of IE is a long-term treatment that requires accurate diagnosis in accordance with pathogens' susceptibility to antibiotics. If the pathogen is not found in culture, broad spectrum antibiotics should be administered to the patient with a double risk of treatment failure and toxicity. However, clinical metagenomics could provide information on antibiotic sensitivity even in the case of a negative culture.
- In most cases, the microbiological diagnosis of IE is not an emergency diagnosis, which is compatible with the use of clinical metagenomics for which the time of implementation is at best 48-72h.
Hence, we propose to assess the performance of clinical metagenomics in the diagnostic of IE.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Age groups
- Adult, Older adult
- Study population
- Adult patient undergoing valvular surgery in the context of suspicion of IE.
Key inclusion criteria (5 listed)
- Age over 18 years-old
- Patient operated for valvular surgery in a context of suspected IE.
- Collection of per-operative samples sent to the central bacteriological laboratory for the purpose of establishing a microbiological diagnosis.
- Obtaining the consent of the patient.
Key exclusion criteria (3 listed)
- Opposition of the patient to participate in the study.
- Insufficient quantity (<500 μL) of sampling to perform conventional analyzes and DNA extraction in this project (may be a secondary exclusion criterion if the patient has already given consent).
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Diagnostic of IE
Time frame: 24 months
The diagnostic of IE obtained by conventional methods and by clinical metagenomics
3 secondary outcomes
Number of species identified by conventional methods but not by clinical metagenomics
Time frame: 24 months
Number of species not identified by conventional methods but found in clinical metagenomics
Time frame: 24 months
Inference of antibiotic susceptibility
Time frame: 24 months
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 28 Apr 2021.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Infective Endocarditis, run by University Hospital, Geneva at 1 site in Switzerland.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 5 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 28 Apr 2021. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Switzerland. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Diagnostic of IE (time frame: 24 months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 28 Apr 2021.