Imaging tuberculosis with endogenous β-lactamase reporter enzyme fluorescence in live mice

Ying Kong, Hequan Yao, Hongjun Ren, Selvakumar Subbian, Suat L.G. Cirillo, James C. Sacchettini, Jianghong Rao, Jeffrey D. Cirillo

Research output: Contribution to journalArticle

118 Citations (Scopus)

Abstract

The slow growth rate and genetic intractability of tubercle bacilli has hindered progress toward understanding tuberculosis, one of the most frequent causes of death worldwide. We overcame this roadblock through development of near-infrared (NIR) fluorogenic substrates for β-lactamase, an enzyme expressed by tubercle bacilli, but not by their eukaryotic hosts, to allow real-time imaging of pulmonary infections and rapid quantification of bacteria in living animals by a strategy called reporter enzyme fluorescence (REF). This strategy has a detection limit of 6 ± 2 × 102 colony-forming units (CFU) of bacteria with the NIR substrate CNIR5 in only 24 h of incubation in vitro, and as few as 104 CFU in the lungs of live mice. REF can also be used to differentiate infected from uninfected macrophages by using confocal microscopy and fluorescence activated cell sorting. Mycobacterium tuberculosis and the bacillus Calmette-Guérin can be tracked directly in the lungs of living mice without sacrificing the animals. Therapeutic efficacy can also be evaluated through loss of REF signal within 24 h posttreatment by using in vitro whole-bacteria assays directly in living mice. We expect that rapid quantification of bacteria within tissues of a living host and in the laboratory is potentially transformative for tuberculosis virulence studies, evaluation of therapeutics, and efficacy of vaccine candidates. This is a unique use of an endogenous bacterial enzyme probe to detect and image tubercle bacilli that demonstrates REF is likely to be useful for the study of many bacterial infections.

Original languageEnglish (US)
Pages (from-to)12239-12244
Number of pages6
JournalProceedings of the National Academy of Sciences of the United States of America
Volume107
Issue number27
DOIs
StatePublished - Jul 6 2010

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Tuberculosis
Fluorescence
Bacillus
Enzymes
Bacteria
Lung
Stem Cells
Fluorescent Dyes
Mycobacterium tuberculosis
Bacterial Infections
Confocal Microscopy
Virulence
Limit of Detection
Cause of Death
Flow Cytometry
Vaccines
Macrophages
Therapeutics
Growth
Infection

All Science Journal Classification (ASJC) codes

  • General

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Imaging tuberculosis with endogenous β-lactamase reporter enzyme fluorescence in live mice. / Kong, Ying; Yao, Hequan; Ren, Hongjun; Subbian, Selvakumar; Cirillo, Suat L.G.; Sacchettini, James C.; Rao, Jianghong; Cirillo, Jeffrey D.

In: Proceedings of the National Academy of Sciences of the United States of America, Vol. 107, No. 27, 06.07.2010, p. 12239-12244.

Research output: Contribution to journalArticle

Kong, Ying ; Yao, Hequan ; Ren, Hongjun ; Subbian, Selvakumar ; Cirillo, Suat L.G. ; Sacchettini, James C. ; Rao, Jianghong ; Cirillo, Jeffrey D. / Imaging tuberculosis with endogenous β-lactamase reporter enzyme fluorescence in live mice. In: Proceedings of the National Academy of Sciences of the United States of America. 2010 ; Vol. 107, No. 27. pp. 12239-12244.
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