Di Chiara Maria, Lazzaro Alessandro, Scribano Daniela, Trancassini Maria, Pietropaolo Valeria, Sonnessa Michele, De Luca Chiara, Prota Rita, Onestà Elisa, Laccetta Gianluigi, Terrin Gianluca
Department of Maternal Infantile and Urological Sciences, Sapienza University of Rome, Viale del Policlinico 155, 00161 Rome, Italy.
Department of Public Health and Infectious Diseases, Sapienza University of Rome, Viale del Policlinico 155, 00161 Rome, Italy.
Trop Med Infect Dis. 2024 Aug 6;9(8):174. doi: 10.3390/tropicalmed9080174.
Microbiota plays a crucial role in intestinal maturation in preterm newborns. The clinical manifestation of the immaturity of the gastro-intestinal tract is called feeding intolerance (FI). This condition may resolve spontaneously or dramatically evolve into necrotizing enterocolitis. One of the most challenging tasks for the neonatologist is to identify those neonates that will develop the disease early in order to adequately provide nutrition to these patients, from the very first hours of life. A close interplay between the maturity of the gastro-intestinal tract and gut microbiota has been described; however, in preterm neonates, this relationship is still undefined. We analyzed the bacterial composition of stool samples, collected early in life, from 30 preterm newborns classified as intolerant or tolerant according to the degree of readiness of the gastro-intestinal tract to receive enteral nutrition. The Pielou evenness index was significantly increased in intolerant compared with tolerant newborns. Data corrected for confounding variables confirmed that the occurrence of gut maturation was independently influenced by Pielou evenness at birth. A lower bacterial diversity very early in life is associated with improved feeding tolerance in preterm newborns. The abundance analysis showed that neonates not ready to receive enteral nutrition for feeding intolerance show, after birth, an increased abundance of , , and . We can argue that those are the taxa that prevent the establishment of pioneer bacteria. A lower alpha-diversity, in the first days of life, may facilitate the seeding of beneficial pioneer bacteria that, in turn, drive healthy microbial colonization during neonatal life.
微生物群在早产儿肠道成熟过程中起着至关重要的作用。胃肠道不成熟的临床表现称为喂养不耐受(FI)。这种情况可能会自行缓解,也可能急剧发展为坏死性小肠结肠炎。新生儿科医生最具挑战性的任务之一是识别那些早期会患上这种疾病的新生儿,以便从生命的最初几个小时就为这些患者充分提供营养。胃肠道成熟与肠道微生物群之间存在密切的相互作用;然而,在早产儿中,这种关系仍不明确。我们分析了30名早产儿出生早期采集的粪便样本的细菌组成,这些早产儿根据胃肠道接受肠内营养的准备程度分为不耐受或耐受组。与耐受组新生儿相比,不耐受组新生儿的皮洛均匀度指数显著升高。校正混杂变量后的数据证实,肠道成熟的发生独立地受到出生时皮洛均匀度的影响。生命早期较低的细菌多样性与早产儿更好的喂养耐受性相关。丰度分析表明,因喂养不耐受而未准备好接受肠内营养的新生儿出生后, 、 、 和 的丰度增加。我们可以认为,这些是阻止先锋细菌定植的分类群。生命最初几天较低的α多样性可能有助于有益先锋细菌的定植,进而在新生儿期推动健康的微生物群落形成。