Intestinal Microbiome Changes in Fecal Microbiota Transplant (FMT) vs. FMT Enriched with Lactobacillus in the Treatment of Recurrent Clostridioides difficile Infection

被引:14
作者
Garza-Gonzalez, Elvira [1 ]
Mendoza-Olazaran, Soraya [1 ]
Morfin-Otero, Rayo [2 ,3 ]
Ramirez-Fontes, Andrea [1 ]
Rodriguez-Zulueta, Patricia [4 ]
Flores-Trevino, Samantha [1 ]
Bocanegra-Ibarias, Paola [1 ]
Maldonado-Garza, Hector [1 ]
Camacho-Ortiz, Adrian [1 ]
机构
[1] Univ Autonoma Nuevo Leon, Fac Med, Hosp Univ Dr Jose Eleuterio Gonzalez, Monterrey, Nuevo Leon, Mexico
[2] Univ Guadalajara, Hosp Civil Guadalajara Fray Antonio Alcalde, Guadalajara, Jalisco, Mexico
[3] Univ Guadalajara, Inst Patol Infecciosa & Expt, Ctr Univ Ciencias Salud, Guadalajara, Jalisco, Mexico
[4] Hosp Gen Manuel Gea Gonzalez, Infect Dis Serv, Ciudad De Mexico, Mexico
关键词
PROBIOTIC COMBINATION; ACIDOPHILUS CL1285; PRIMARY PREVENTION; CASEI LBC80R; COLONOSCOPY; FECES;
D O I
10.1155/2019/4549298
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Aim. In this study, we conducted a comparative study to explore the differences in therapeutic efficacy and intestinal microbiome of fecal microbiota transplant (FMT) vs. FMT in addition with Lactobacillus (FMT-L) for treatment of recurrent Clostridioides difficile infection (R-CDI). Methods. We designed a double-blinded randomized comparative two-arm pilot multicenter study to assess the efficacy and impact in the intestinal microbiome of standard capsules of FMT vs. FMT-L enriched with 3 species of Lactobacillus for patients with R-CDI. A 90-day follow-up of 21 patients was performed, starting at the beginning of the study. From the selected patients, fecal samples were obtained at days 0, 3, 7, and 28 after treatment. Fecal samples and FMT were analyzed by 16S rRNA sequencing. Results. We included 21 patients (13 in the FMT group and 8 in the FMT-L group). Overall, both groups had a reduction in bowel movements per day, from 8.6 to 3.2 in the first 48 h (62.7% reduction, p=0.001). No severe adverse reactions or recurrences were recorded. Firmicutes were the most abundant phylum in donors. A low relative abundance of Proteobacteria was detected and mostly found in patients even at higher proportions than the donor. The donor's pool also had relatively few Bacteroidetes, and some patients showed a higher abundance of this phylum. Based on the ANOSIM R values, there is a significant difference between the microbial communities of basal samples and samples collected on day 7 (p=0.045) and at day 28 (0.041). Conclusion. Fecal microbiota transplant by capsules was clinically and genomically similar between traditional FMT and enriched FMT with Lactobacillus spp. Restoration of bacterial diversity and resolution of dysbiosis at days 7 and 28 were observed. Patients with a first episode of recurrence treated with FMT had an excellent response without severe adverse events; FMT should be considered as an early treatment during R-CDI.
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页数:7
相关论文
共 12 条
[1]   Fecal Microbiota Transplantation Capsules with Targeted Colonic Versus Gastric Delivery in Recurrent Clostridium difficile Infection: A Comparative Cohort Analysis of High and Lose Dose [J].
Allegretti, Jessica R. ;
Fischer, Monika ;
Sagi, Sashidhar, V ;
Bohm, Matthew E. ;
Fadda, Hala M. ;
Ranmal, Sejal R. ;
Budree, Shrish ;
Basit, Abdul W. ;
Glettig, Dean L. ;
de la Serna, Eva L. ;
Gentile, Amanda ;
Gerardin, Ylaine ;
Timberlake, Sonia ;
Sadovsky, Rotem ;
Smith, Mark ;
Kassam, Zain .
DIGESTIVE DISEASES AND SCIENCES, 2019, 64 (06) :1672-1678
[2]   Lactobacillus acidophilus CL1285, Lactobacillus casei LBC80R, and Lactobacillus rhamnosus CLR2 (Bio-K+): Characterization, Manufacture, Mechanisms of Action, and Quality Control of a Specific Probiotic Combination for Primary Prevention of Clostridium difficile Infection [J].
Auclair, Julie ;
Frappier, Martin ;
Millette, Mathieu .
CLINICAL INFECTIOUS DISEASES, 2015, 60 :S135-S143
[3]   Randomised clinical trial: faecal microbiota transplantation by colonoscopy vs. vancomycin for the treatment of recurrent Clostridium difficile infection [J].
Cammarota, G. ;
Masucci, L. ;
Ianiro, G. ;
Bibbo, S. ;
Dinoi, G. ;
Costamagna, G. ;
Sanguinetti, M. ;
Gasbarrini, A. .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2015, 41 (09) :835-843
[4]   Ultra-high-throughput microbial community analysis on the Illumina HiSeq and MiSeq platforms [J].
Caporaso, J. Gregory ;
Lauber, Christian L. ;
Walters, William A. ;
Berg-Lyons, Donna ;
Huntley, James ;
Fierer, Noah ;
Owens, Sarah M. ;
Betley, Jason ;
Fraser, Louise ;
Bauer, Markus ;
Gormley, Niall ;
Gilbert, Jack A. ;
Smith, Geoff ;
Knight, Rob .
ISME JOURNAL, 2012, 6 (08) :1621-1624
[5]  
Gutierrez-Delgado EM, 2016, ACTA GASTRO-ENT BELG, V79, P268
[6]   Standardized Frozen Preparation for Transplantation of Fecal Microbiota for Recurrent Clostridium difficile Infection [J].
Hamilton, Matthew J. ;
Weingarden, Alexa R. ;
Sadowsky, Michael J. ;
Khoruts, Alexander .
AMERICAN JOURNAL OF GASTROENTEROLOGY, 2012, 107 (05) :761-767
[7]   Fecal Transplantation, Through Colonoscopy, Is Effective Therapy for Recurrent Clostridium difficile Infection [J].
Mattila, Eero ;
Uusitalo-Seppala, Raija ;
Wuorela, Maarit ;
Lehtola, Laura ;
Nurmi, Heimo ;
Ristikankare, Matti ;
Moilanen, Veikko ;
Salminen, Kimmo ;
Seppala, Maaria ;
Mattila, Petri S. ;
Anttila, Veli-Jukka ;
Arkkila, Perttu .
GASTROENTEROLOGY, 2012, 142 (03) :490-496
[8]   A Decade of Experience in Primary Prevention of Clostridium difficile Infection at a Community Hospital Using the Probiotic Combination Lactobacillus acidophilus CL1285, Lactobacillus casei LBC80R, and Lactobacillus rhamnosus CLR2 (Bio-K+) [J].
Maziade, Pierre-Jean ;
Pereira, Pascale ;
Goldstein, Ellie J. C. .
CLINICAL INFECTIOUS DISEASES, 2015, 60 :S144-S147
[9]  
McDonald LC, 2018, CLIN INFECT DIS, V66, pE1, DOI [10.1093/cid/cix1085, 10.1093/cid/ciy149]
[10]   Clostridium difficile infection: molecular pathogenesis and novel therapeutics [J].
Rineh, Ardeshir ;
Kelso, Michael J. ;
Vatansever, Fatma ;
Tegos, George P. ;
Hamblin, Michael R. .
EXPERT REVIEW OF ANTI-INFECTIVE THERAPY, 2014, 12 (01) :131-150