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A core microbiome associated with the peritoneal tumors of pseudomyxoma peritonei

机译:腹膜假粘液瘤腹膜肿瘤相关的核心微生物组

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Background Pseudomyxoma peritonei (PMP) is a malignancy characterized by dissemination of mucus-secreting cells throughout the peritoneum. This disease is associated with significant morbidity and mortality and despite effective treatment options for early-stage disease, patients with PMP often relapse. Thus, there is a need for additional treatment options to reduce relapse rate and increase long-term survival. A previous study identified the presence of both typed and non-culturable bacteria associated with PMP tissue and determined that increased bacterial density was associated with more severe disease. These findings highlighted the possible role for bacteria in PMP disease. Methods To more clearly define the bacterial communities associated with PMP disease, we employed a sequenced-based analysis to profile the bacterial populations found in PMP tumor and mucin tissue in 11 patients. Sequencing data were confirmed by in situ hybridization at multiple taxonomic depths and by culturing. A pilot clinical study was initiated to determine whether the addition of antibiotic therapy affected PMP patient outcome. Main results We determined that the types of bacteria present are highly conserved in all PMP patients; the dominant phyla are the Proteobacteria, Actinobacteria, Firmicutes and Bacteroidetes. A core set of taxon-specific sequences were found in all 11 patients; many of these sequences were classified into taxonomic groups that also contain known human pathogens. In situ hybridization directly confirmed the presence of bacteria in PMP at multiple taxonomic depths and supported our sequence-based analysis. Furthermore, culturing of PMP tissue samples allowed us to isolate 11 different bacterial strains from eight independent patients, and in vitro analysis of subset of these isolates suggests that at least some of these strains may interact with the PMP-associated mucin MUC2. Finally, we provide evidence suggesting that targeting these bacteria with antibiotic treatment may increase the survival of PMP patients. Conclusions Using 16S amplicon-based sequencing, direct in situ hybridization analysis and culturing methods, we have identified numerous bacterial taxa that are consistently present in all PMP patients tested. Combined with data from a pilot clinical study, these data support the hypothesis that adding antimicrobials to the standard PMP treatment could improve PMP patient survival.
机译:背景腹膜假单胞菌(PMP)是一种恶性肿瘤,其特征是在整个腹膜中散布着粘液分泌细胞。该疾病与显着的发病率和死亡率有关,尽管对早期疾病有有效的治疗选择,但PMP患者经常复发。因此,需要额外的治疗选择以降低复发率并增加长期存活率。先前的研究确定了与PMP组织相关的类型细菌和不可培养细菌的存在,并确定细菌密度增加与更严重的疾病有关。这些发现强调了细菌在PMP疾病中的可能作用。方法为了更清楚地定义与PMP疾病相关的细菌群落,我们采用了基于序列的分析方法,对11例患者的PMP肿瘤和粘蛋白组织中的细菌种群进行了分析。通过在多个分类学深度的原位杂交并通过培养来证实测序数据。开始了一项初步临床研究,以确定添加抗生素治疗是否会影响PMP患者的预后。主要结果我们确定,在所有PMP患者中,存在的细菌类型都是高度保守的。主要的门是变形杆菌,放线菌,硬毛和拟杆菌。在所有11名患者中发现了一组核心的分类单元特异性序列。这些序列中有许多被分类为也包含已知人类病原体的分类组。原位杂交直接证实了PMP中多种分类深度的细菌的存在,并支持了我们基于序列的分析。此外,PMP组织样品的培养使我们能够从8名独立患者中分离出11种不同的细菌菌株,这些分离株的子集的体外分析表明,这些菌株中的至少一些可能与PMP相关的粘蛋白MUC2相互作用。最后,我们提供的证据表明,用抗生素治疗靶向这些细菌可以提高PMP患者的生存率。结论使用基于16S扩增子的测序,直接原位杂交分析和培养方法,我们确定了在所有接受测试的PMP患者中始终存在的众多细菌类群。结合来自临床试验研究的数据,这些数据支持以下假设,即在标准PMP治疗中添加抗菌药物可以改善PMP患者的生存率。

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