Long-Term Impact of Suppressive Antibiotic Therapy on Intestinal Microbiota

被引:8
作者
Escudero-Sanchez, Rosa [1 ,2 ]
Ponce-Alonso, Manuel [2 ,3 ]
Barragan-Prada, Hugo [3 ]
Morosini, Maria Isabel [2 ,3 ]
Canton, Rafael [2 ,3 ]
Cobo, Javier [1 ,2 ]
del Campo, Rosa [2 ,3 ]
机构
[1] Hosp Univ Ramon y Cajal, Serv Enfermedades Infecciosas, Inst Ramon y Cajal Invest Sanitaria IRYCIS, Madrid, Spain
[2] Hosp Univ Ramon y Cajal, Red Espanola Invest Patol Infecciosa, Madrid, Spain
[3] Hosp Univ Ramon y Cajal, Serv Microbiol, Inst Ramon y Cajal Invest Sanitaria IRYCIS, Madrid, Spain
关键词
suppressive antibiotic therapy; gut microbiota; PCR-DGGE; bacterial viability; propidium monoazide; antibiotic multirresistant colonization; GUT MICROBIOTA; RECOVERY;
D O I
10.3390/genes12010041
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The aim was to describe the safety of indefinite administration of antibiotics, the so-called suppressive antibiotic therapy (SAT) and to provide insight into their impact on gut microbiota. 17 patients with SAT were recruited, providing a fecal sample. Bacterial composition was determined by 16S rDNA massive sequencing, and their viability was explored by PCR-DGGE with and without propidium monoazide. Presence of antibiotic multirresistant bacteria was explored through the culture of feces in selective media. High intra-individual variability in the genera distribution regardless of the antibiotic or antibiotic administration ingestion period, with few statistically significant differences detected by Bray-Curtis distance-based principle component analysis, permutational multivariate analysis of variance and linear discriminant analysis effect size analysis. However, the microbiota composition of patients treated with both beta-lactams and sulfonamides clustered by a heat map. Curiously, the detection of antibiotic resistant bacteria was almost anecdotic and CTX-M-15-producing E. coli were detected in two subjects. Our work demonstrates the overall clinical safety of SAT and the low rate of the selection of multidrug-resistant bacteria triggered by this therapy. We also describe the composition of intestinal microbiota under the indefinite use of antibiotics for the first time.
引用
收藏
页码:1 / 13
页数:13
相关论文
共 39 条
[1]   RETRACTED: Abnormal Weight Gain and Gut Microbiota Modifications Are Side Effects of Long-Term Doxycycline and Hydroxychloroquine Treatment (Publication with Expression of Concern. See vol. 66, 2022) (Retracted Article) [J].
Angelakis, Emmanouil ;
Million, Matthieu ;
Kankoe, Sallah ;
Lagier, Jean-Christophe ;
Armougom, Fabrice ;
Giorgi, Roch ;
Raoult, Didier .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2014, 58 (06) :3342-3347
[2]   Antibiotic-Induced Changes in the Intestinal Microbiota and Disease [J].
Becattini, Simone ;
Taur, Ying ;
Pamer, Eric G. .
TRENDS IN MOLECULAR MEDICINE, 2016, 22 (06) :458-478
[3]   AN ORDINATION OF THE UPLAND FOREST COMMUNITIES OF SOUTHERN WISCONSIN [J].
BRAY, JR ;
CURTIS, JT .
ECOLOGICAL MONOGRAPHS, 1957, 27 (04) :326-349
[4]   Impact of Antibiotic Gut Exposure on the Temporal Changes in Microbiome Diversity [J].
Burdet, Charles ;
Thu Thuy Nguyen ;
Duval, Xavier ;
Ferreira, Stephanie ;
Andremont, Antoine ;
Guedj, Jeremie ;
Mentre, France ;
Ait-Ilalne, B. ;
Alavoine, L. ;
Duval, X. ;
Ecobichon, J. L. ;
Ilic-Habensus, E. ;
Laparra, A. ;
Nisus, M. E. ;
Ralaimazava, P. ;
Raine, S. ;
Tubiana, S. ;
Vignali, V. ;
Chachaty, E. .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2019, 63 (10)
[5]  
Burdet C, 2017, ANTIMICROB AGENTS CH, V61, DOI [10.1128/AAC.00543-17, 10.1128/aac.00543-17]
[6]   QIIME allows analysis of high-throughput community sequencing data [J].
Caporaso, J. Gregory ;
Kuczynski, Justin ;
Stombaugh, Jesse ;
Bittinger, Kyle ;
Bushman, Frederic D. ;
Costello, Elizabeth K. ;
Fierer, Noah ;
Pena, Antonio Gonzalez ;
Goodrich, Julia K. ;
Gordon, Jeffrey I. ;
Huttley, Gavin A. ;
Kelley, Scott T. ;
Knights, Dan ;
Koenig, Jeremy E. ;
Ley, Ruth E. ;
Lozupone, Catherine A. ;
McDonald, Daniel ;
Muegge, Brian D. ;
Pirrung, Meg ;
Reeder, Jens ;
Sevinsky, Joel R. ;
Tumbaugh, Peter J. ;
Walters, William A. ;
Widmann, Jeremy ;
Yatsunenko, Tanya ;
Zaneveld, Jesse ;
Knight, Rob .
NATURE METHODS, 2010, 7 (05) :335-336
[7]   Incomplete recovery and individualized responses of the human distal gut microbiota to repeated antibiotic perturbation [J].
Dethlefsen, Les ;
Relman, David A. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2011, 108 :4554-4561
[8]   Gut microbiota disturbance during antibiotic therapy: a multi-omic approach [J].
Elena Perez-Cobas, Ana ;
Jose Gosalbes, Maria ;
Friedrichs, Anette ;
Knecht, Henrik ;
Artacho, Alejandro ;
Eismann, Kathleen ;
Otto, Wolfgang ;
Rojo, David ;
Bargiela, Rafael ;
von Bergen, Martin ;
Neulinger, Sven C. ;
Daeumer, Carolin ;
Heinsen, Femke-Anouska ;
Latorre, Amparo ;
Barbas, Coral ;
Seifert, Jana ;
dos Santos, Vitor Martins ;
Ott, Stephan J. ;
Ferrer, Manuel ;
Moya, Andres .
GUT, 2013, 62 (11) :1591-1601
[9]   Suppressive antibiotic therapy in prosthetic joint infections: a multicentre cohort study [J].
Escudero-Sanchez, R. ;
Senneville, E. ;
Digumber, M. ;
Soriano, A. ;
del Toro, M. D. ;
Bahamonde, A. ;
del Pozo, J. L. ;
Guio, L. ;
Murillo, O. ;
Rico, A. ;
Garcia-Pais, M. J. ;
Rodriguez-Pardo, D. ;
Iribarren, J. A. ;
Fernandez, M. ;
Benito, N. ;
Fresco, G. ;
Muriel, A. ;
Ariza, J. ;
Cobo, J. .
CLINICAL MICROBIOLOGY AND INFECTION, 2020, 26 (04) :499-505
[10]   High-Throughput Sequencing Reveals the Incomplete, Short-Term Recovery of Infant Gut Microbiota following Parenteral Antibiotic Treatment with Ampicillin and Gentamicin [J].
Fouhy, Fiona ;
Guinane, Caitriona M. ;
Hussey, Seamus ;
Wall, Rebecca ;
Ryan, C. Anthony ;
Dempsey, Eugene M. ;
Murphy, Brendan ;
Ross, R. Paul ;
Fitzgerald, Gerald F. ;
Stanton, Catherine ;
Cotter, Paul D. .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2012, 56 (11) :5811-5820