Broad-spectrum respiratory tract pathogen identification using resequencing DNA microarrays

被引:102
作者
Lin, BC
Wang, Z
Vora, GJ
Thornton, JA
Schnur, JM
Thach, DC
Blaney, KM
Ligler, AG
Malanoski, AP
Santiago, J
Walter, EA
Agan, BK
Metzgar, D
Seto, D
Daum, LT
Kruzelock, R
Rowley, RK
Hanson, EH
Tibbetts, C
Stenger, DA
机构
[1] USN, Res Lab, Ctr Biomol Sci & Engn, Washington, DC 20375 USA
[2] NOVA Res Inc, Alexandria, VA 22308 USA
[3] Lackland AFB, Epidem Outbreak Surveillance Adv Diagnost Lab, San Antonio, TX 78236 USA
[4] Texas A&M Univ Syst, San Antonio, TX 78223 USA
[5] Wilford Hall USAF Med Ctr, Dept Infect Dis, Lackland AFB, San Antonio, TX 78236 USA
[6] USN, Hlth Res Ctr, US Dept Def, Ctr Deployment Hlth Res, San Diego, CA 92186 USA
[7] George Mason Univ, Sch Computat Sci, Manassas, VA 20110 USA
[8] USAF, HQ, SGR, Falls Church, VA 22041 USA
[9] USAF, Inst Operat Hlth, Brooks AFB, San Antonio, TX 78235 USA
关键词
D O I
10.1101/gr.4337206
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
The exponential growth of pathogen nucleic acid sequences available in public domain databases has invited their direct use in pathogen detection, identification, and surveillance strategies. DNA microarray technology has offered the potential for the direct DNA sequence analysis of a broad spectrum of pathogens of interest. However, to achieve the practical attainment of this potential, numerous technical issues, especially nucleic acid amplification, probe specificity, and interpretation strategies of sequence detection, need to be addressed. In this report, we demonstrate an approach that combines the use of a custom-designed Affymetrix resequencing Respiratory Pathogen Microarray (RPM v.1) with methods for microbial nucleic acid enrichment, random nucleic acid amplification, and automated sequence similarity searching for broad-spectrum respiratory pathogen surveillance. Successful proof-of-concept experiments, utilizing clinical samples obtained from patients presenting adenovirus or influenza virus-induced febrile respiratory illness (FRI), demonstrate the ability of this approach for correct species- and strain-level identification with unambiguous statistical interpretation at clinically relevant sensitivity levels. Our results underscore the feasibility of using this approach to expedite the early surveillance of diseases, and provide new information on the incidence of multiple pathogens.
引用
收藏
页码:527 / 535
页数:9
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