Abstract
The coronavirus disease 2019 (COVID-19) pandemic is a challenge for ongoing efforts to combat antimicrobial-resistant (AMR) bacterial infections. As we learn more about COVID-19 disease and drug stewardship evolves, there is likely to be a lasting impact of increased use of antimicrobial agents and antibiotics, as well as a lack of consistent access to health care across many populations. Sexually transmitted infections have been underreported during the pandemic and are often caused by some of the most drug-resistant pathogens. In their recent article in mBio, Parzych et al. (E. M. Parzych, S. Gulati, B. Zheng, M. A. Bah, et al., mBio 12:e00242-21, 2021, https://doi.org/10.1128/mBio.00242-21) focus on protection against Neisseria gonorrhoeae infection via in vivo delivery of an antigonococcal DNA-encoded antibody that has been modified for increased complement activation. Nucleic acid approaches are highly adaptable and could be tremendously beneficial for personalized strategies to combat AMR pathogens.
| Original language | English |
|---|---|
| Article number | e00473-21 |
| Journal | mBio |
| Volume | 12 |
| Issue number | 4 |
| DOIs | |
| Publication status | Published - 20 Jul 2021 |
| Externally published | Yes |
Keywords
- AMR
- Antimicrobial resistance
- Bacteria
- DNA-encoded antibodies
- Geneencoded antibodies
- Personalized medicine
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