Translational Global Infectious Disease Research Center, University of Vermont, Burlington, Vermont, United States of America.
Department of Microbiology and Molecular Genetics, University of Vermont, Burlington, Vermont, United States of America.
PLoS Comput Biol. 2023 Nov 22;19(11):e1011624. doi: 10.1371/journal.pcbi.1011624. eCollection 2023 Nov.
Despite significant progress in recent decades toward ameliorating the excess burden of diarrheal disease globally, childhood diarrhea remains a leading cause of morbidity and mortality in low-and-middle-income countries (LMICs). Recent large-scale studies of diarrhea etiology in these populations have revealed widespread co-infection with multiple enteric pathogens, in both acute and asymptomatic stool specimens. We applied methods from network science and ecology to better understand the underlying structure of enteric co-infection among infants in two large longitudinal birth cohorts in Bangladesh. We used a configuration model to establish distributions of expected random co-occurrence, based on individual pathogen prevalence alone, for every pathogen pair among 30 enteropathogens detected by qRT-PCR in both diarrheal and asymptomatic stool specimens. We found two pairs, Enterotoxigenic E. coli (ETEC) with Enteropathogenic E. coli (EPEC), and ETEC with Campylobacter spp., co-infected significantly more than expected at random (both pairs co-occurring almost 4 standard deviations above what one could expect due to chance alone). Furthermore, we found a general pattern that bacteria-bacteria pairs appear together more frequently than expected at random, while virus-bacteria pairs tend to appear less frequently than expected based on model predictions. Finally, infants co-infected with leading bacteria-bacteria pairs had more days of diarrhea in the first year of life compared to infants without co-infection (p-value <0.0001). Our methods and results help us understand the structure of enteric co-infection which can guide further work to identify and eliminate common sources of infection or determine biologic mechanisms that promote co-infection.
尽管在最近几十年中,全球在改善腹泻病负担方面取得了重大进展,但在中低收入国家(LMICs),儿童腹泻仍然是发病率和死亡率的主要原因。最近对这些人群腹泻病因的大规模研究表明,在急性和无症状粪便标本中,广泛存在多种肠道病原体的共同感染。我们应用网络科学和生态学的方法,更好地理解孟加拉国两个大型纵向出生队列中婴儿肠道共同感染的潜在结构。我们使用配置模型,根据个体病原体的单独流行率,为在腹泻和无症状粪便标本中通过 qRT-PCR 检测到的 30 种肠道病原体中的每对病原体建立随机共同发生的预期分布。我们发现两对病原体,肠毒性大肠杆菌(ETEC)和肠致病性大肠杆菌(EPEC),以及 ETEC 和弯曲杆菌属,共同感染的频率明显高于随机预期(这两对病原体的共同出现频率比仅因偶然因素而预期的高近 4 个标准差)。此外,我们发现了一种普遍模式,即细菌-细菌对比随机预期更频繁地一起出现,而病毒-细菌对则比基于模型预测的更不频繁地出现。最后,与没有共同感染的婴儿相比,同时感染主要细菌-细菌对的婴儿在生命的第一年腹泻的天数更多(p 值<0.0001)。我们的方法和结果帮助我们理解肠道共同感染的结构,这可以指导进一步的工作,以确定和消除常见的感染源,或确定促进共同感染的生物学机制。