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Published on: January 5, 2024
Threat and Control of tet(X)-Mediated Tigecycline-Resistant Acinetobacter sp. Bacteria
Chong Chen1,2, Taotao Wu1,2, Jing Liu1,2
1Joint International Research Laboratory of Agriculture and Agri-Product Safety, Institutes of Agricultural Science and Technology Development, Yangzhou University, Yangzhou 225009, China.
Abstract:
Tigecycline is regarded as one of the last-resort antibiotics against multidrug-resistant (MDR) Acinetobacter sp. bacteria. Recently, the tigecycline-resistant Acinetobacter sp. isolates mediated by tet(X) genes have emerged as a class of global pathogens for humans and food-producing animals. However, the genetic diversities and treatment options were not systematically discussed in the era of One Health. In this review, we provide a detailed illustration of the evolution route, distribution characteristics, horizontal transmission, and rapid detection of tet(X) genes in diverse Acinetobacter species. We also detail the application of chemical drugs, plant extracts, phages, antimicrobial peptides (AMPs), and CRISPR-Cas technologies for controlling tet(X)-positive Acinetobacter sp. pathogens. Despite excellent activities, the antibacterial spectrum and application safety need further evaluation and resolution. It is noted that deep learning is a promising approach to identify more potent antimicrobial compounds.
Insights
Tigecycline resistance in Acinetobacter is rising due to tet(X) genes. This review explores tet(X) gene diversity and control strategies for these global pathogens.
Area of Science:
- Microbiology
- Genetics
- One Health
Background:
- Tigecycline is a crucial antibiotic for multidrug-resistant (MDR) Acinetobacter.
- Emergence of tigecycline-resistant Acinetobacter mediated by tet(X) genes poses a global health threat.
- Lack of systematic discussion on tet(X) gene diversity and treatment options under the One Health framework.
Purpose of the Study:
- To comprehensively review the evolution, distribution, transmission, and detection of tet(X) genes in Acinetobacter species.
- To explore various therapeutic strategies for controlling tet(X)-positive Acinetobacter pathogens.
- To highlight the potential of deep learning in discovering novel antimicrobial compounds.
Main Methods:
- Literature review focusing on tet(X) genes in Acinetobacter.
- Analysis of genetic diversity, geographical distribution, and horizontal gene transfer mechanisms.
- Evaluation of chemical drugs, plant extracts, bacteriophages, antimicrobial peptides (AMPs), and CRISPR-Cas systems for therapeutic applications.
Main Results:
- Detailed illustration of tet(X) gene evolution, distribution, and detection methods.
- Discussion of diverse control strategies including conventional drugs and novel approaches like phages and AMPs.
- Identification of deep learning as a promising avenue for antimicrobial discovery.
Conclusions:
- tet(X)-mediated tigecycline resistance in Acinetobacter is a growing concern requiring integrated One Health strategies.
- Various therapeutic options show promise but require further evaluation for efficacy and safety.
- Advanced computational methods like deep learning offer potential for future antimicrobial development.
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