Enzymes in Synergy: Bacteria Specific Molecular Probe for Locoregional Imaging of Urinary Tract Infection in vivo

Author:

Xin Evelias Yan Hui1,Kwek Germain1,An Xiaoyu23,Sun Caixia1,Liu Songhan1,Qing Ng Shuang1,Lingesh Shonya1,Jiang Lai24,Liu Gang23,Xing Bengang1ORCID

Affiliation:

1. School of Chemistry, Chemical Engineering and Biotechnology Nanyang Technological University 21 Nanyang Link S637371 Singapore Singapore

2. State Key Laboratory of Vaccines for Infectious Diseases, Center for Molecular Imaging and Translational Medicine, Xiang An Biomedicine Laboratory, National Innovation Platform for Industry-Education Integration in Vaccine Research, School of Public Health Xiamen University 4221 Xiangan Road, Xiang'an District Xiamen, Fujian 361102 China

3. State Key Laboratory of Cellular Stress Biology, School of Life Sciences Xiamen University 4221 Xianganan Road, Xiang'an District Xiamen, Fujian 361102 China

4. School of Pharmaceutical Sciences Zhejiang Chinese Medical University 260 Baichuan Road, Fuyang District Hangzhou, Zhejiang 311402 China

Abstract

AbstractUropathogenic Escherichia coli (UPECs) is a leading cause for urinary tract infections (UTI), accounting for 70–90 % of community or hospital‐acquired bacterial infections owing to high recurrence, imprecision in diagnosis and management, and increasing prevalence of antibiotic resistance. Current methods for clinical UPECs detection still rely on labor‐intensive urine cultures that impede rapid and accurate diagnosis for timely UTI therapeutic management. Herein, we developed a first‐in‐class near‐infrared (NIR) UPECs fluorescent probe (NO−AH) capable of specifically targeting UPECs through its collaborative response to bacterial enzymes, enabling locoregional imaging of UTIs both in vitro and in vivo. Our NO−AH probe incorporates a dual protease activatable moiety, which first reacts with OmpT, an endopeptidase abundantly present on the outer membrane of UPECs, releasing an intermediate amino acid residue conjugated with a NIR hemicyanine fluorophore. Such liberated fragment would be subsequently recognized by aminopeptidase (APN) within the periplasm of UPECs, activating localized fluorescence for precise imaging of UTIs in complex living environments. The peculiar specificity and selectivity of NO−AH, facilitated by the collaborative action of bacterial enzymes, features a timely and accurate identification of UPECs‐infected UTIs, which could overcome misdiagnosis in conventional urine tests, thus opening new avenues towards reliable UTI diagnosis and personalized antimicrobial therapy management.

Funder

Nanyang Technological University

National Natural Science Foundation of China

Publisher

Wiley

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