Academic Journal

The gut microbiome in sickle cell disease: Characterization and potential implications

التفاصيل البيبلوغرافية
العنوان: The gut microbiome in sickle cell disease: Characterization and potential implications
المؤلفون: Brim, Hassan, Taylor, James, Abbas, Muneer, Vilmenay, Kimberly, Daremipouran, Mohammad, Varma, Sudhir, Lee, Edward, Pace, Betty, Song-Naba, Waogwende L., Gupta, Kalpna, Nekhai, Sergei, O’Neil, Patricia, Ashktorab, Hassan
المساهمون: Ishaq, Suzanne L., National Heart, Lung, and Blood Institute, National Center on Minority Health and Health Disparities, National Institutes of Health, national institutes of health
المصدر: PLOS ONE ; volume 16, issue 8, page e0255956 ; ISSN 1932-6203
بيانات النشر: Public Library of Science (PLoS)
سنة النشر: 2021
المجموعة: PLOS Publications (via CrossRef)
الوصف: Background Sickle Cell Disease (SCD) is an inherited blood disorder that leads to hemolytic anemia, pain, organ damage and early mortality. It is characterized by polymerized deoxygenated hemoglobin, rigid sickle red blood cells and vaso-occlusive crises (VOC). Recurrent hypoxia-reperfusion injury in the gut of SCD patients could increase tissue injury, permeability, and bacterial translocation. In this context, the gut microbiome, a major player in health and disease, might have significant impact. This study sought to characterize the gut microbiome in SCD. Methods Stool and saliva samples were collected from healthy controls (n = 14) and SCD subjects (n = 14). Stool samples were also collected from humanized SCD murine models including Berk, Townes and corresponding control mice. Amplified 16S rDNA was used for bacterial composition analysis using Next Generation Sequencing (NGS). Pairwise group analyses established differential bacterial groups at many taxonomy levels. Bacterial group abundance and differentials were established using DeSeq software. Results A major dysbiosis was observed in SCD patients. The Firmicutes/Bacteroidetes ratio was lower in these patients. The following bacterial families were more abundant in SCD patients: Acetobacteraceae, Acidaminococcaceae, Candidatus Saccharibacteria, Peptostreptococcaceae, Bifidobacteriaceae, Veillonellaceae, Actinomycetaceae, Clostridiales, Bacteroidacbactereae and Fusobacteriaceae. This dysbiosis translated into 420 different operational taxonomic units (OTUs). Townes SCD mice also displayed gut microbiome dysbiosis as seen in human SCD. Conclusion A major dysbiosis was observed in SCD patients for bacteria that are known strong pro-inflammatory triggers. The Townes mouse showed dysbiosis as well and might serve as a good model to study gut microbiome modulation and its impact on SCD pathophysiology.
نوع الوثيقة: article in journal/newspaper
اللغة: English
DOI: 10.1371/journal.pone.0255956
الاتاحة: http://dx.doi.org/10.1371/journal.pone.0255956
https://dx.plos.org/10.1371/journal.pone.0255956
Rights: http://creativecommons.org/licenses/by/4.0/
رقم الانضمام: edsbas.6B2BA392
قاعدة البيانات: BASE
الوصف
DOI:10.1371/journal.pone.0255956