Usability of rectal swabs for microbiome sampling in a cohort study of hematological and oncological patients

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Usability of rectal swabs for microbiome sampling in a cohort study of hematological and oncological patients. / Biehl, Lena M; Garzetti, Debora; Farowski, Fedja; Ring, Diana; Koeppel, Martin B; Rohde, Holger; Schafhausen, Philippe; Stecher, Bärbel; Vehreschild, Maria J G T.

in: PLOS ONE, Jahrgang 14, Nr. 4, 2019, S. e0215428.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Biehl, LM, Garzetti, D, Farowski, F, Ring, D, Koeppel, MB, Rohde, H, Schafhausen, P, Stecher, B & Vehreschild, MJGT 2019, 'Usability of rectal swabs for microbiome sampling in a cohort study of hematological and oncological patients', PLOS ONE, Jg. 14, Nr. 4, S. e0215428. https://doi.org/10.1371/journal.pone.0215428

APA

Biehl, L. M., Garzetti, D., Farowski, F., Ring, D., Koeppel, M. B., Rohde, H., Schafhausen, P., Stecher, B., & Vehreschild, M. J. G. T. (2019). Usability of rectal swabs for microbiome sampling in a cohort study of hematological and oncological patients. PLOS ONE, 14(4), e0215428. https://doi.org/10.1371/journal.pone.0215428

Vancouver

Bibtex

@article{b57dafaa235b4ac599aad6de7c45e8fa,
title = "Usability of rectal swabs for microbiome sampling in a cohort study of hematological and oncological patients",
abstract = "OBJECTIVES: Large-scale clinical studies investigating associations between intestinal microbiota signatures and human diseases usually rely on stool samples. However, the timing of repeated stool sample collection cannot be predefined in longitudinal settings. Rectal swabs, being straightforward to obtain, have the potential to overcome this drawback. Therefore, we assessed the usability of rectal swabs for microbiome sampling in a cohort of hematological and oncological patients.STUDY DESIGN: We used a pipeline for intestinal microbiota analysis from deep rectal swabs which was established and validated with test samples and negative controls. Consecutively, a cohort of patients from hematology and oncology wards was established and weekly deep rectal swabs taken during their admissions and re-admissions.RESULTS: Validation of our newly developed pipeline for intestinal microbiota analysis from rectal swabs revealed consistent and reproducible results. Over a period of nine months, 418 rectal swabs were collected longitudinally from 41 patients. Adherence to the intended sampling protocol was 97%. After DNA extraction, sequencing, read pre-processing and filtering of chimeric sequences, 405 of 418 samples (96.9%) were eligible for further analyses. Follow-up samples and those taken under current antibiotic exposure showed a significant decrease in alpha diversity as compared to baseline samples. Microbial domination occurred most frequently by Enterococcaceae (99 samples, 24.4%) on family level and Enterococcus (90 samples, 22.2%) on genus level. Furthermore, we noticed a high abundance of potential skin commensals in 99 samples (24.4%).SUMMARY: Deep rectal swabs were shown to be reliable for microbiome sampling and analysis, with practical advantages related to high sampling adherence, easy timing, transport and storage. The relatively high abundance of putative skin commensals in this patient cohort may be of potential interest and should be further investigated. Generally, previous findings on alpha diversity dynamics obtained from stool samples were confirmed.",
author = "Biehl, {Lena M} and Debora Garzetti and Fedja Farowski and Diana Ring and Koeppel, {Martin B} and Holger Rohde and Philippe Schafhausen and B{\"a}rbel Stecher and Vehreschild, {Maria J G T}",
year = "2019",
doi = "10.1371/journal.pone.0215428",
language = "English",
volume = "14",
pages = "e0215428",
journal = "PLOS ONE",
issn = "1932-6203",
publisher = "Public Library of Science",
number = "4",

}

RIS

TY - JOUR

T1 - Usability of rectal swabs for microbiome sampling in a cohort study of hematological and oncological patients

AU - Biehl, Lena M

AU - Garzetti, Debora

AU - Farowski, Fedja

AU - Ring, Diana

AU - Koeppel, Martin B

AU - Rohde, Holger

AU - Schafhausen, Philippe

AU - Stecher, Bärbel

AU - Vehreschild, Maria J G T

PY - 2019

Y1 - 2019

N2 - OBJECTIVES: Large-scale clinical studies investigating associations between intestinal microbiota signatures and human diseases usually rely on stool samples. However, the timing of repeated stool sample collection cannot be predefined in longitudinal settings. Rectal swabs, being straightforward to obtain, have the potential to overcome this drawback. Therefore, we assessed the usability of rectal swabs for microbiome sampling in a cohort of hematological and oncological patients.STUDY DESIGN: We used a pipeline for intestinal microbiota analysis from deep rectal swabs which was established and validated with test samples and negative controls. Consecutively, a cohort of patients from hematology and oncology wards was established and weekly deep rectal swabs taken during their admissions and re-admissions.RESULTS: Validation of our newly developed pipeline for intestinal microbiota analysis from rectal swabs revealed consistent and reproducible results. Over a period of nine months, 418 rectal swabs were collected longitudinally from 41 patients. Adherence to the intended sampling protocol was 97%. After DNA extraction, sequencing, read pre-processing and filtering of chimeric sequences, 405 of 418 samples (96.9%) were eligible for further analyses. Follow-up samples and those taken under current antibiotic exposure showed a significant decrease in alpha diversity as compared to baseline samples. Microbial domination occurred most frequently by Enterococcaceae (99 samples, 24.4%) on family level and Enterococcus (90 samples, 22.2%) on genus level. Furthermore, we noticed a high abundance of potential skin commensals in 99 samples (24.4%).SUMMARY: Deep rectal swabs were shown to be reliable for microbiome sampling and analysis, with practical advantages related to high sampling adherence, easy timing, transport and storage. The relatively high abundance of putative skin commensals in this patient cohort may be of potential interest and should be further investigated. Generally, previous findings on alpha diversity dynamics obtained from stool samples were confirmed.

AB - OBJECTIVES: Large-scale clinical studies investigating associations between intestinal microbiota signatures and human diseases usually rely on stool samples. However, the timing of repeated stool sample collection cannot be predefined in longitudinal settings. Rectal swabs, being straightforward to obtain, have the potential to overcome this drawback. Therefore, we assessed the usability of rectal swabs for microbiome sampling in a cohort of hematological and oncological patients.STUDY DESIGN: We used a pipeline for intestinal microbiota analysis from deep rectal swabs which was established and validated with test samples and negative controls. Consecutively, a cohort of patients from hematology and oncology wards was established and weekly deep rectal swabs taken during their admissions and re-admissions.RESULTS: Validation of our newly developed pipeline for intestinal microbiota analysis from rectal swabs revealed consistent and reproducible results. Over a period of nine months, 418 rectal swabs were collected longitudinally from 41 patients. Adherence to the intended sampling protocol was 97%. After DNA extraction, sequencing, read pre-processing and filtering of chimeric sequences, 405 of 418 samples (96.9%) were eligible for further analyses. Follow-up samples and those taken under current antibiotic exposure showed a significant decrease in alpha diversity as compared to baseline samples. Microbial domination occurred most frequently by Enterococcaceae (99 samples, 24.4%) on family level and Enterococcus (90 samples, 22.2%) on genus level. Furthermore, we noticed a high abundance of potential skin commensals in 99 samples (24.4%).SUMMARY: Deep rectal swabs were shown to be reliable for microbiome sampling and analysis, with practical advantages related to high sampling adherence, easy timing, transport and storage. The relatively high abundance of putative skin commensals in this patient cohort may be of potential interest and should be further investigated. Generally, previous findings on alpha diversity dynamics obtained from stool samples were confirmed.

U2 - 10.1371/journal.pone.0215428

DO - 10.1371/journal.pone.0215428

M3 - SCORING: Journal article

C2 - 30986251

VL - 14

SP - e0215428

JO - PLOS ONE

JF - PLOS ONE

SN - 1932-6203

IS - 4

ER -