Tran Na T D, Chaidee Apisit, Surapinit Achirawit, Yingklang Manachai, Roytrakul Sitiruk, Charoenlappanit Sawanya, Pinlaor Porntip, Hongsrichan Nuttanan, Nguyen Thi Hai, Anutrakulchai Sirirat, Cha'on Ubon, Pinlaor Somchai
Department of Parasitology, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand.
Faculty of Medical Laboratory Science, Danang University of Medical Technology and Pharmacy, Danang, Viet Nam.
Heliyon. 2023 Sep 6;9(9):e19859. doi: 10.1016/j.heliyon.2023.e19859. eCollection 2023 Sep.
Understanding gut bacterial composition and proteome changes in patients with early-stage chronic kidney disease (CKD) could lead to better methods of controlling the disease progression. Here, we investigated the gut microbiome and microbial functions in patients with infection (strongyloidiasis) and early-stage CKD. Thirty-five patients with early stages (1-3) of CKD were placed in two groups matched for population characteristics and biochemical parameters, 12 patients with strongyloidiasis in one group and 23 uninfected patients in the other. From every individual, a sample of their feces was obtained and processed for 16S rRNA sequencing and metaproteomic analysis using tandem liquid chromatography-mass spectrometry (LC-MS/MS). infection per se did not significantly alter gut microbial diversity. However, certain genera (, , , , and ) were significantly more abundant in infection-free CKD patients than in infected individuals. The genera and were enriched in infected patients. Among the significantly altered genera, and were the most correlated with renal parameters. The relative abundance of members of the genus was moderately positively correlated with estimated glomerular filtration rate (eGFR) (r = 0.335, p = 0.049) and negatively with serum creatinine (r = -0.35, p = 0.039). , on the other hand, showed a near-significant positive correlation with eGFR (r = 0.296, p = 0.084). Individuals with infection had higher levels of bacterial proteins involved in amino-acid metabolism. Analysis using STITCH predicted that bacterial amino-acid metabolism may also be involved in the production of colon-derived uremic toxin (indole), a toxic substance known to promote CKD. infection is, therefore, associated with reduced abundance of and (two genera possibly beneficial for kidney function) and with increased bacterial amino-acid metabolism in the early-stages of CKD, potentially producing uremic toxin. This study provides useful information for prevention of progression of CKD beyond the early stages.
了解早期慢性肾脏病(CKD)患者的肠道细菌组成和蛋白质组变化,可能会带来更好的控制疾病进展的方法。在此,我们研究了感染(类圆线虫病)患者和早期CKD患者的肠道微生物群及其功能。35例CKD早期(1 - 3期)患者按人口统计学特征和生化参数匹配分为两组,一组12例类圆线虫病患者,另一组23例未感染患者。从每位患者采集粪便样本,采用串联液相色谱 - 质谱联用(LC - MS/MS)进行16S rRNA测序和宏蛋白质组分析。感染本身并未显著改变肠道微生物多样性。然而,某些菌属([具体菌属1]、[具体菌属2]、[具体菌属3]、[具体菌属4]和[具体菌属5])在未感染CKD患者中的丰度显著高于感染个体。[具体菌属6]和[具体菌属7]在感染患者中富集。在显著改变的菌属中,[具体菌属8]和[具体菌属9]与肾脏参数的相关性最强。[具体菌属10]成员的相对丰度与估计肾小球滤过率(eGFR)呈中度正相关(r = 0.335,p = 0.049),与血清肌酐呈负相关(r = -0.35,p = 0.039)。另一方面,[具体菌属11]与eGFR呈接近显著的正相关(r = 0.296,p = 0.084)。感染[具体病原体]的个体参与氨基酸代谢的细菌蛋白水平较高。使用STITCH进行的分析预测,细菌氨基酸代谢可能也参与结肠源性尿毒症毒素(吲哚)的产生,吲哚是一种已知会促进CKD的有毒物质。因此,在CKD早期,感染[具体病原体]与[具体菌属12]和[具体菌属13](可能对肾功能有益的两个菌属)丰度降低以及细菌氨基酸代谢增加有关,这可能会产生尿毒症毒素。本研究为预防CKD早期阶段后的疾病进展提供了有用信息。