Laboratório de Imunorregulação, iREG, Departamento de Microbiologia, Imunologia e Parasitologia, Universidade Federal de Santa Catarina, Campus Universitário da Trindade, Florianópolis 88034-040, SC, Brazil.
Laboratório de Imunologia Aplicada, Departamento de Microbiologia, Imunologia e Parasitologia, Universidade Federal de Santa Catarina, Campus Universitário da Trindade, Florianópolis 88034-040, SC, Brazil.
Cells. 2022 Jul 23;11(15):2278. doi: 10.3390/cells11152278.
Childhood malnutrition affects physiology and development. It increases infection rates, which may not present clinical signs in severe cases. The World Health Organization recommends prophylactic treatment with cotrimoxazole (SXT) and nutritional recovery to overcome this issue. This treatment is controversial, since evidence of a reduction in morbidity and mortality is not a consensus and could induce the development of antibiotic-resistant bacteria. Moreover, the impact of using this wide-spectrum antibiotic on gut microbiota in a critical period of development, and weakness is unknown. To understand how SXT prophylaxis could affect gut microbiota in undernutrition, we induced protein-energy undernutrition (PEU) in weaning C57BL/6 mice for three weeks and treated animals with SXT for two weeks. Using 16S rRNA gene sequencing, we compared the taxonomic composition and metabolic pathways of control mice, animals submitted to undernutrition (UND), treated with SXT, or undernourished and SXT treated (UND + SXT). We identified that UND mice had a significant increase in predicted pathways related to metabolic syndromes later in life. The prophylactic SXT treatment alone resulted in a significant loss in community richness and beta diversity. Furthermore, we identified the reduction of three genera in SXT treated mice, including the butyrate producers and . Both UND and double challenge (UND + SXT) resulted in a reduction of the amino acid's biosynthesis pathway related to cell growth. Our results show that the SXT prophylaxis of young mice during an undernourishment period did not re-establish the undernourished microbiota community composition similar to healthy controls but induced a distinct dysbiotic profile with functional metabolic consequences.
儿童营养不良会影响生理和发育。它会增加感染率,在严重的情况下,这些感染可能没有临床症状。世界卫生组织建议使用复方新诺明(SXT)进行预防性治疗和营养恢复,以克服这一问题。这种治疗存在争议,因为减少发病率和死亡率的证据尚未达成共识,并且可能会诱导产生抗生素耐药菌。此外,在发育的关键时期,使用这种广谱抗生素对肠道微生物群的影响以及其潜在弱点尚不清楚。为了了解 SXT 预防如何影响营养不良的肠道微生物群,我们在断奶的 C57BL/6 小鼠中诱导了蛋白质-能量营养不良(PEU),并使用 SXT 治疗了两周。通过 16S rRNA 基因测序,我们比较了对照组、营养不良组(UND)、SXT 治疗组或营养不良和 SXT 治疗组(UND + SXT)的分类组成和代谢途径。我们发现,UND 小鼠在生命后期与代谢综合征相关的预测途径显著增加。单独预防性 SXT 治疗会导致群落丰富度和β多样性显著丧失。此外,我们发现 SXT 处理的小鼠中有三个属减少,包括丁酸盐产生菌 和 。UND 和双重挑战(UND + SXT)都导致与细胞生长相关的氨基酸生物合成途径减少。我们的研究结果表明,在营养不良期间,年轻小鼠的 SXT 预防并未使营养不良的微生物群落组成恢复到类似于健康对照组的水平,而是诱导了一种具有功能代谢后果的不同的生态失调特征。