Paulson Joseph N, Williams Brent L, Hehnly Christine, Mishra Nischay, Sinnar Shamim A, Zhang Lijun, Ssentongo Paddy, Mbabazi-Kabachelor Edith, Wijetunge Dona S S, von Bredow Benjamin, Mulondo Ronnie, Kiwanuka Julius, Bajunirwe Francis, Bazira Joel, Bebell Lisa M, Burgoine Kathy, Couto-Rodriguez Mara, Ericson Jessica E, Erickson Tim, Ferrari Matthew, Gladstone Melissa, Guo Cheng, Haran Murali, Hornig Mady, Isaacs Albert M, Kaaya Brian Nsubuga, Kangere Sheila M, Kulkarni Abhaya V, Kumbakumba Elias, Li Xiaoxiao, Limbrick David D, Magombe Joshua, Morton Sarah U, Mugamba John, Ng James, Olupot-Olupot Peter, Onen Justin, Peterson Mallory R, Roy Farrah, Sheldon Kathryn, Townsend Reid, Weeks Andrew D, Whalen Andrew J, Quackenbush John, Ssenyonga Peter, Galperin Michael Y, Almeida Mathieu, Atkins Hannah, Warf Benjamin C, Lipkin W Ian, Broach James R, Schiff Steven J
Department of Biostatistics, Product Development, Genentech Inc., South San Francisco, CA 94080, USA.
Center for Infection and Immunity, Mailman School of Public Health, Columbia University, New York, NY 10032, USA.
Sci Transl Med. 2020 Sep 30;12(563). doi: 10.1126/scitranslmed.aba0565.
Postinfectious hydrocephalus (PIH), which often follows neonatal sepsis, is the most common cause of pediatric hydrocephalus worldwide, yet the microbial pathogens underlying this disease remain to be elucidated. Characterization of the microbial agents causing PIH would enable a shift from surgical palliation of cerebrospinal fluid (CSF) accumulation to prevention of the disease. Here, we examined blood and CSF samples collected from 100 consecutive infant cases of PIH and control cases comprising infants with non-postinfectious hydrocephalus in Uganda. Genomic sequencing of samples was undertaken to test for bacterial, fungal, and parasitic DNA; DNA and RNA sequencing was used to identify viruses; and bacterial culture recovery was used to identify potential causative organisms. We found that infection with the bacterium , together with frequent cytomegalovirus (CMV) coinfection, was associated with PIH in our infant cohort. Assembly of the genome of a facultative anaerobic bacterial isolate recovered from cultures of CSF samples from PIH cases identified a strain of This strain, designated Mbale, was lethal when injected into mice in contrast to the benign reference strain. These findings show that an unbiased pan-microbial approach enabled characterization of in CSF samples from PIH cases, and point toward a pathway of more optimal treatment and prevention for PIH and other proximate neonatal infections.
感染后脑积水(PIH)通常继发于新生儿败血症,是全球儿童脑积水最常见的病因,但该疾病背后的微生物病原体仍有待阐明。对导致PIH的微生物病原体进行特征描述,将使治疗从针对脑脊液(CSF)积聚的手术缓解转向疾病预防。在此,我们检测了从乌干达100例连续的PIH婴儿病例以及包括非感染后脑积水婴儿的对照病例中采集的血液和脑脊液样本。对样本进行基因组测序以检测细菌、真菌和寄生虫DNA;使用DNA和RNA测序来鉴定病毒;并通过细菌培养回收来鉴定潜在的致病生物。我们发现,在我们的婴儿队列中,感染该细菌以及频繁的巨细胞病毒(CMV)合并感染与PIH有关。从PIH病例的脑脊液样本培养物中分离出的一种兼性厌氧细菌的基因组组装鉴定出一株该菌株,命名为姆巴莱,与良性参考菌株相比,将其注射到小鼠体内时具有致死性。这些发现表明,一种无偏见的泛微生物方法能够对PIH病例脑脊液样本中的该细菌进行特征描述,并为PIH和其他相近的新生儿感染指明了一条更优化的治疗和预防途径。