Modeling of Urinary Microbiota Associated With Cystitis
A decade ago, when the Human Microbiome Project was starting, urinary tract (UT) was not included because the bladder and urine were considered to be sterile. Today, we are presented with evidence that healthy UT possesses native microbiota and any major event disrupting its “equilibrium” can impact...
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Published in | Frontiers in cellular and infection microbiology Vol. 11; p. 643638 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
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16.03.2021
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Abstract | A decade ago, when the Human Microbiome Project was starting, urinary tract (UT) was not included because the bladder and urine were considered to be sterile. Today, we are presented with evidence that healthy UT possesses native microbiota and any major event disrupting its “equilibrium” can impact the host also. This dysbiosis often leads to cystitis symptoms, which is the most frequent lower UT complaint, especially among women. Cystitis is one of the most common causes of antimicrobial drugs prescriptions in primary and secondary care and an important contributor to the problem of antimicrobial resistance. Despite this fact, we still have trouble distinguishing whether the primary cause of majority of cystitis cases is a single pathogen overgrowth, or a systemic disorder affecting entire UT microbiota. There are relatively few studies monitoring changes and dynamics of UT microbiota in cystitis patients, making this field of research still an unknown. In this study variations to the UT microbiota of cystitis patients were identified and microbial dynamics has been modeled. The microbial genetic profile of urine samples from 28 patients was analyzed by 16S rDNA Illumina sequencing and bioinformatics analysis. One patient with bacterial cystitis symptoms was prescribed therapy based on national guideline recommendations on antibacterial treatment of urinary tract infections (UTI) and UT microbiota change was monitored by 16S rDNA sequencing on 24 h basis during the entire therapy duration. The results of sequencing implied that a particular class of bacteria is associated with majority of cystitis cases in this study. The contributing role of this class of bacteria –
Gammaproteobacteria
, was further predicted by generalized Lotka-Volterra modeling (gLVM). Longitudinal microbiota insight obtained from a single patient under prescribed antimicrobial therapy revealed rapid and extensive changes in microbial composition and emphasized the need for current guidelines revision in regards to therapy duration. Models based on gLVM indicated protective role of two taxonomic classes of bacteria,
Actinobacteria
and
Bacteroidia
class, which appear to actively suppress pathogen overgrowth. |
---|---|
AbstractList | A decade ago, when the Human Microbiome Project was starting, urinary tract (UT) was not included because the bladder and urine were considered to be sterile. Today, we are presented with evidence that healthy UT possesses native microbiota and any major event disrupting its "equilibrium" can impact the host also. This dysbiosis often leads to cystitis symptoms, which is the most frequent lower UT complaint, especially among women. Cystitis is one of the most common causes of antimicrobial drugs prescriptions in primary and secondary care and an important contributor to the problem of antimicrobial resistance. Despite this fact, we still have trouble distinguishing whether the primary cause of majority of cystitis cases is a single pathogen overgrowth, or a systemic disorder affecting entire UT microbiota. There are relatively few studies monitoring changes and dynamics of UT microbiota in cystitis patients, making this field of research still an unknown. In this study variations to the UT microbiota of cystitis patients were identified and microbial dynamics has been modeled. The microbial genetic profile of urine samples from 28 patients was analyzed by 16S rDNA Illumina sequencing and bioinformatics analysis. One patient with bacterial cystitis symptoms was prescribed therapy based on national guideline recommendations on antibacterial treatment of urinary tract infections (UTI) and UT microbiota change was monitored by 16S rDNA sequencing on 24 h basis during the entire therapy duration. The results of sequencing implied that a particular class of bacteria is associated with majority of cystitis cases in this study. The contributing role of this class of bacteria -
, was further predicted by generalized Lotka-Volterra modeling (gLVM). Longitudinal microbiota insight obtained from a single patient under prescribed antimicrobial therapy revealed rapid and extensive changes in microbial composition and emphasized the need for current guidelines revision in regards to therapy duration. Models based on gLVM indicated protective role of two taxonomic classes of bacteria,
and
class, which appear to actively suppress pathogen overgrowth. A decade ago, when the Human Microbiome Project was starting, urinary tract (UT) was not included because the bladder and urine were considered to be sterile. Today, we are presented with evidence that healthy UT possesses native microbiota and any major event disrupting its “equilibrium” can impact the host also. This dysbiosis often leads to cystitis symptoms, which is the most frequent lower UT complaint, especially among women. Cystitis is one of the most common causes of antimicrobial drugs prescriptions in primary and secondary care and an important contributor to the problem of antimicrobial resistance. Despite this fact, we still have trouble distinguishing whether the primary cause of majority of cystitis cases is a single pathogen overgrowth, or a systemic disorder affecting entire UT microbiota. There are relatively few studies monitoring changes and dynamics of UT microbiota in cystitis patients, making this field of research still an unknown. In this study variations to the UT microbiota of cystitis patients were identified and microbial dynamics has been modeled. The microbial genetic profile of urine samples from 28 patients was analyzed by 16S rDNA Illumina sequencing and bioinformatics analysis. One patient with bacterial cystitis symptoms was prescribed therapy based on national guideline recommendations on antibacterial treatment of urinary tract infections (UTI) and UT microbiota change was monitored by 16S rDNA sequencing on 24 h basis during the entire therapy duration. The results of sequencing implied that a particular class of bacteria is associated with majority of cystitis cases in this study. The contributing role of this class of bacteria – Gammaproteobacteria , was further predicted by generalized Lotka-Volterra modeling (gLVM). Longitudinal microbiota insight obtained from a single patient under prescribed antimicrobial therapy revealed rapid and extensive changes in microbial composition and emphasized the need for current guidelines revision in regards to therapy duration. Models based on gLVM indicated protective role of two taxonomic classes of bacteria, Actinobacteria and Bacteroidia class, which appear to actively suppress pathogen overgrowth. A decade ago, when the Human Microbiome Project was starting, urinary tract (UT) was not included because the bladder and urine were considered to be sterile. Today, we are presented with evidence that healthy UT possesses native microbiota and any major event disrupting its "equilibrium" can impact the host also. This dysbiosis often leads to cystitis symptoms, which is the most frequent lower UT complaint, especially among women. Cystitis is one of the most common causes of antimicrobial drugs prescriptions in primary and secondary care and an important contributor to the problem of antimicrobial resistance. Despite this fact, we still have trouble distinguishing whether the primary cause of majority of cystitis cases is a single pathogen overgrowth, or a systemic disorder affecting entire UT microbiota. There are relatively few studies monitoring changes and dynamics of UT microbiota in cystitis patients, making this field of research still an unknown. In this study variations to the UT microbiota of cystitis patients were identified and microbial dynamics has been modeled. The microbial genetic profile of urine samples from 28 patients was analyzed by 16S rDNA Illumina sequencing and bioinformatics analysis. One patient with bacterial cystitis symptoms was prescribed therapy based on national guideline recommendations on antibacterial treatment of urinary tract infections (UTI) and UT microbiota change was monitored by 16S rDNA sequencing on 24 h basis during the entire therapy duration. The results of sequencing implied that a particular class of bacteria is associated with majority of cystitis cases in this study. The contributing role of this class of bacteria - Gammaproteobacteria, was further predicted by generalized Lotka-Volterra modeling (gLVM). Longitudinal microbiota insight obtained from a single patient under prescribed antimicrobial therapy revealed rapid and extensive changes in microbial composition and emphasized the need for current guidelines revision in regards to therapy duration. Models based on gLVM indicated protective role of two taxonomic classes of bacteria, Actinobacteria and Bacteroidia class, which appear to actively suppress pathogen overgrowth.A decade ago, when the Human Microbiome Project was starting, urinary tract (UT) was not included because the bladder and urine were considered to be sterile. Today, we are presented with evidence that healthy UT possesses native microbiota and any major event disrupting its "equilibrium" can impact the host also. This dysbiosis often leads to cystitis symptoms, which is the most frequent lower UT complaint, especially among women. Cystitis is one of the most common causes of antimicrobial drugs prescriptions in primary and secondary care and an important contributor to the problem of antimicrobial resistance. Despite this fact, we still have trouble distinguishing whether the primary cause of majority of cystitis cases is a single pathogen overgrowth, or a systemic disorder affecting entire UT microbiota. There are relatively few studies monitoring changes and dynamics of UT microbiota in cystitis patients, making this field of research still an unknown. In this study variations to the UT microbiota of cystitis patients were identified and microbial dynamics has been modeled. The microbial genetic profile of urine samples from 28 patients was analyzed by 16S rDNA Illumina sequencing and bioinformatics analysis. One patient with bacterial cystitis symptoms was prescribed therapy based on national guideline recommendations on antibacterial treatment of urinary tract infections (UTI) and UT microbiota change was monitored by 16S rDNA sequencing on 24 h basis during the entire therapy duration. The results of sequencing implied that a particular class of bacteria is associated with majority of cystitis cases in this study. The contributing role of this class of bacteria - Gammaproteobacteria, was further predicted by generalized Lotka-Volterra modeling (gLVM). Longitudinal microbiota insight obtained from a single patient under prescribed antimicrobial therapy revealed rapid and extensive changes in microbial composition and emphasized the need for current guidelines revision in regards to therapy duration. Models based on gLVM indicated protective role of two taxonomic classes of bacteria, Actinobacteria and Bacteroidia class, which appear to actively suppress pathogen overgrowth. A decade ago, when the Human Microbiome Project was starting, urinary tract (UT) was not included because the bladder and urine were considered to be sterile. Today, we are presented with evidence that healthy UT possesses native microbiota and any major event disrupting its “equilibrium” can impact the host also. This dysbiosis often leads to cystitis symptoms, which is the most frequent lower UT complaint, especially among women. Cystitis is one of the most common causes of antimicrobial drugs prescriptions in primary and secondary care and an important contributor to the problem of antimicrobial resistance. Despite this fact, we still have trouble distinguishing whether the primary cause of majority of cystitis cases is a single pathogen overgrowth, or a systemic disorder affecting entire UT microbiota. There are relatively few studies monitoring changes and dynamics of UT microbiota in cystitis patients, making this field of research still an unknown. In this study variations to the UT microbiota of cystitis patients were identified and microbial dynamics has been modeled. The microbial genetic profile of urine samples from 28 patients was analyzed by 16S rDNA Illumina sequencing and bioinformatics analysis. One patient with bacterial cystitis symptoms was prescribed therapy based on national guideline recommendations on antibacterial treatment of urinary tract infections (UTI) and UT microbiota change was monitored by 16S rDNA sequencing on 24 h basis during the entire therapy duration. The results of sequencing implied that a particular class of bacteria is associated with majority of cystitis cases in this study. The contributing role of this class of bacteria – Gammaproteobacteria, was further predicted by generalized Lotka-Volterra modeling (gLVM). Longitudinal microbiota insight obtained from a single patient under prescribed antimicrobial therapy revealed rapid and extensive changes in microbial composition and emphasized the need for current guidelines revision in regards to therapy duration. Models based on gLVM indicated protective role of two taxonomic classes of bacteria, Actinobacteria and Bacteroidia class, which appear to actively suppress pathogen overgrowth. |
Author | Barisic, Karmela Ceprnja, Marina Svetlicic, Ema Zucko, Jurica Starcevic, Lucija Starcevic, Antonio Oros, Damir Skrlin, Jasenka Melvan, Ena |
AuthorAffiliation | 1 Biochemical Laboratory, Special Hospital Agram, Polyclinic Zagreb , Zagreb , Croatia 5 Department for Clinical Microbiology and Hospital Infection, University Hospital Dubrava , Zagreb , Croatia 3 Laboratory for Bioinformatics, Faculty of Food Technology and Biotechnology, Zagreb University , Zagreb , Croatia 4 Department of Biological Science, Faculty of Science, Macquarie University , Sydney, NSW , Australia 2 Department of Medical Biochemistry and Hematology, Faculty of Pharmacy and Biochemistry, Zagreb University , Zagreb , Croatia |
AuthorAffiliation_xml | – name: 2 Department of Medical Biochemistry and Hematology, Faculty of Pharmacy and Biochemistry, Zagreb University , Zagreb , Croatia – name: 1 Biochemical Laboratory, Special Hospital Agram, Polyclinic Zagreb , Zagreb , Croatia – name: 3 Laboratory for Bioinformatics, Faculty of Food Technology and Biotechnology, Zagreb University , Zagreb , Croatia – name: 5 Department for Clinical Microbiology and Hospital Infection, University Hospital Dubrava , Zagreb , Croatia – name: 4 Department of Biological Science, Faculty of Science, Macquarie University , Sydney, NSW , Australia |
Author_xml | – sequence: 1 givenname: Marina surname: Ceprnja fullname: Ceprnja, Marina – sequence: 2 givenname: Damir surname: Oros fullname: Oros, Damir – sequence: 3 givenname: Ena surname: Melvan fullname: Melvan, Ena – sequence: 4 givenname: Ema surname: Svetlicic fullname: Svetlicic, Ema – sequence: 5 givenname: Jasenka surname: Skrlin fullname: Skrlin, Jasenka – sequence: 6 givenname: Karmela surname: Barisic fullname: Barisic, Karmela – sequence: 7 givenname: Lucija surname: Starcevic fullname: Starcevic, Lucija – sequence: 8 givenname: Jurica surname: Zucko fullname: Zucko, Jurica – sequence: 9 givenname: Antonio surname: Starcevic fullname: Starcevic, Antonio |
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Cites_doi | 10.1186/s12866-018-1379-1 10.3389/fcimb.2013.00041 10.1007/s11884-016-0345-8 10.1136/ewjm.176.1.51 10.1128/JCM.02876-13 10.1038/nrmicro3432 10.1186/s40168-019-0729-z 10.1128/mBio.00218-20 10.1093/jtm/taz036 10.1016/j.tibtech.2019.12.021 10.1186/s12014-020-09289-4 10.1371/journal.pone.0093827 10.1016/j.ajog.2015.05.032 10.1093/jac/dkv020 10.1097/MOU.0000000000000396 10.1186/1479-5876-10-174 10.1038/s41598-019-46078-y 10.1371/journal.pone.0014116 10.15252/msb.20178157 10.1038/s41587-019-0209-9 10.1038/s41598-018-22660-8 10.1002/14651858.CD004682.pub2 10.1038/nrurol.2014.361 10.4137/BBI.S12462 10.1128/JCM.05852-11 10.1017/CBO9781139173179 10.1038/nmeth.3869 10.1038/s41585-018-0104-z 10.1097/GCO.0000000000000298 10.1038/nature08821 10.1038/ismej.2011.139 10.1186/1471-2180-12-205 10.1186/s40168-017-0305-3 10.1128/JCM.02452-13 |
ContentType | Journal Article |
Copyright | Copyright © 2021 Ceprnja, Oros, Melvan, Svetlicic, Skrlin, Barisic, Starcevic, Zucko and Starcevic. Copyright © 2021 Ceprnja, Oros, Melvan, Svetlicic, Skrlin, Barisic, Starcevic, Zucko and Starcevic 2021 Ceprnja, Oros, Melvan, Svetlicic, Skrlin, Barisic, Starcevic, Zucko and Starcevic |
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Keywords | therapy duration microbial interaction modeling antibiotics microbiome 16S rRNA sequencing urinary tract infection |
Language | English |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Edited by: Alan J. Wolfe, Loyola University Chicago, United States This article was submitted to Microbiome in Health and Disease, a section of the journal Frontiers in Cellular and Infection Microbiology Reviewed by: Qunfeng Dong, Loyola University Chicago, United States; Linda Brubaker, University of San Diego, United States |
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SubjectTerms | 16S rRNA sequencing antibiotics Cellular and Infection Microbiology microbial interaction modeling microbiome therapy duration urinary tract infection |
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Title | Modeling of Urinary Microbiota Associated With Cystitis |
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