Case Studies of the Spatial Heterogeneity of DNA Viruses in the Cystic Fibrosis Lung

被引:80
作者
Willner, Dana [1 ,3 ,4 ]
Haynes, Matthew R. [1 ]
Furlan, Mike [1 ]
Hanson, Nicole [1 ]
Kirby, Breeann [1 ]
Lim, Yan Wei [1 ]
Rainey, Paul B. [5 ,6 ,7 ]
Schmieder, Robert [1 ,2 ]
Youle, Merry [8 ]
Conrad, Douglas [9 ,10 ]
Rohwer, Forest [1 ,11 ]
机构
[1] San Diego State Univ, Dept Biol, San Diego, CA 92182 USA
[2] San Diego State Univ, Computat Sci Res Ctr, San Diego, CA 92182 USA
[3] Univ Queensland, Sch Chem & Mol Biosci, Australian Ctr Ecogen, Brisbane, Qld, Australia
[4] Univ Queensland, Sch Chem & Mol Biosci, Diamantina Inst, Brisbane, Qld, Australia
[5] Massey Univ, New Zealand Inst Adv Study, Auckland, New Zealand
[6] Massey Univ, Allan Wilson Ctr Mol Ecol & Evolut, Auckland, New Zealand
[7] Max Planck Inst Evolutionary Biol, Plon, Germany
[8] Rainbow Rock, Ocean View, HI USA
[9] Univ Calif San Diego, Dept Med, La Jolla, CA 92093 USA
[10] San Diego Vet Adm Healthcare Syst, San Diego, CA USA
[11] Ctr Microbial Sci, San Diego, CA USA
关键词
cystic fibrosis; viruses; metagenomics; antibiotic resistance; ANTIBIOTIC-RESISTANCE; PULMONARY-FUNCTION; VIRAL COMMUNITIES; BACTERIOPHAGE; INFORMATION; DIVERSITY; SEQUENCE;
D O I
10.1165/rcmb.2011-0253OC
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Microbial communities in the lungs of patients with cystic fibrosis (CF) and chronic obstructive pulmonary disease (COPD) have been shown to be spatially heterogeneous. Viral communities may also vary spatially, leading to localized viral populations and infections. Here, we characterized viral communities from multiple areas of the lungs of two patients with late-stage CF using metagenomics, that is, the explanted lungs from a transplant patient and lungs acquired postmortem. All regions harbored eukaryotic viruses that may infect the human host, notably herpesviruses, anelloviruses, and papillomaviruses. In the highly diseased apical lobes of explant lungs, viral diversity was extremely low, and only eukaryotic viruses were present. The absence of phage suggests that CF-associated microbial biofilms may escape top-down controls by phage predation. The phages present in other lobes of explant lungs and in all lobes of postmortem lungs comprised distinct communities, and encoded genes for clinically important microbial phenotypes, including small colony variants and antibiotic resistance. Based on the these observations, we postulate that viral communities in CF lungs are spatially distinct and contribute to CF pathology by augmenting the metabolic potential of resident microbes, as well as by directly damaging lung tissue via carcinomas and herpesviral outbreaks.
引用
收藏
页码:127 / 131
页数:5
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