Background: Acute pancreatitis (AP) has a broad spectrum of severity and is associated with considerable morbidity and mortality. We aimed to evaluate the composition and functional effects of gut microbiota in different grades of AP severity.Results: Gut microbiota in AP patients was characterized by decreased species richness. The most representative gut microbiota in mild acute pancreatitis (MAP), moderately severe acute pancreatitis (MSAP), and severe acute pancreatitis (SAP) was Streptococcus, Escherichia-coli, and Enterococcus, respectively. Each of the three AP-associated genera could differentiate AP from healthy control population. Representative pathways associated with the glutathione metabolism, lipopolysaccharide biosynthesis, and amino acid metabolism (valine, leucine and isoleucine degradation) were enriched in MAP, MSAP, and SAP, respectively.Conclusions: Our ndings indicate that in patients with AP, the gut microbiome composition and function are correlated with different severity of AP from a whole-genome perspective, and new changes are observed.
BackgroundAcute pancreatitis (AP) is the most common gastrointestinal disease that requires acute admission and causes tremendous pain and socioeconomic burden [1]. The worldwide incidence of AP ranges from 4.9 to 80 cases per 100,000 individuals annually [2]. According to the Revised Atlanta Classi cation, AP is strati ed into mild acute pancreatitis (MAP), moderately severe acute pancreatitis (MSAP), and severe acute pancreatitis (SAP) [3]. The outcome of AP patients with different severity is widely divergent. For instance, patients with MAP only need supportive care such as uid and analgesia and recover within a few days. But in the non-mild form of AP, an in ammatory cascade usually leads to local and systemic complications, claims remarkable morbidity and mortality, and makes the management of AP challenging [4]. The pathogenetic mechanism underlying the progression of AP severity is yet to be elucidated [5].Gut microbiota plays an essential role in maintaining immune homeostasis and the biological barrier of the intestine [6]. Under pathological conditions such as AP, perturbations to the gut microbiota could disrupt gut barrier, increase the intestinal permeability, and lead to bacterial translocation, which in turn triggers secondary infectious complications [7]. Several bacteria, including Escherichia, Shigella, Enterococcus, and Enterobacteriaceae family, have been found in the pancreas, indicating that their translocation from the gut could lead to infected pancreatic necrosis in non-mild AP [8]. Our previous work revealed different gut bacteria composition in AP patients with varying grades of severity. To be speci c, Bacteroides, Escherichis-Shigella, and Enterococcus was the dominant gut microbiota species in MAP, MSAP, and SAP, respectively. Besides, Anaerococcus and Enterococcus were signi cantly increased and Eubacterium hallii decreased in non-mild AP patients [9]. Similar ndings were also reported by Zhu Y et al. [7]. These studies ...