loading page

Prolonged viral shedding in an immunocompromised Korean patient infected with hMPXV, sub-lineage B.1.3, with acquired drug resistant mutations during tecovirimat treatment
  • +7
  • Yoon-Seok Chung,
  • Minji Lee,
  • Chi-Hwan Choi,
  • Jin-Won Kim,
  • Gyuri Sim,
  • SangEun Lee,
  • Hwachul Shin,
  • Jeong hyun Lee,
  • Myung-Min Choi,
  • Hwajung Yi
Yoon-Seok Chung
Korea Disease Control and Prevention Agency

Corresponding Author:[email protected]

Author Profile
Minji Lee
Korea Disease Control and Prevention Agency
Author Profile
Chi-Hwan Choi
Korea Disease Control and Prevention Agency
Author Profile
Jin-Won Kim
Korea Disease Control and Prevention Agency
Author Profile
Gyuri Sim
Korea Disease Control and Prevention Agency
Author Profile
SangEun Lee
Korea Disease Control and Prevention Agency
Author Profile
Hwachul Shin
Korea Disease Control and Prevention Agency
Author Profile
Jeong hyun Lee
Korea Disease Control and Prevention Agency
Author Profile
Myung-Min Choi
Korea Disease Control and Prevention Agency
Author Profile
Hwajung Yi
Korea Disease Control and Prevention Agency
Author Profile

Abstract

Following the worldwide surge in mpox(monkeypox) in 2022, cases have persisted in Asia, including South Korea, and sexual contact is presumed as the predominant mode of transmission, with a discernible surge in prevalence among immunocompromised patients. Drugs such as tecovirimat can result in drug-resistant mutations, presenting obstacles to treatment. This study aimed to ascertain the presence of tecovirimat-related resistant mutations through genomic analysis of the monkeypox virus isolated from a reported case involving prolonged viral shedding in South Korea. Here, tecovirimat-resistant mutations, previously identified in the B.1 clade, were observed in the B.1.3 clade, predominant in South Korea. These mutations exhibited diverse patterns across different samples from the same patient and reflected the varied distribution of viral subpopulations in different anatomical regions. The A290V and A288P mutant strains we isolated hold promise for elucidating these mechanisms, enabling a comprehensive analysis of viral pathogenesis, replication strategies, and host interactions. Our findings imply that acquired drug-resistant mutations, may present a challenge to individual patient treatment. Moreover, they have the potential to give rise to transmitted drug-resistant mutations, thereby imposing a burden on the public health system. Consequently, the meticulous genomic surveillance among immunocompromised patients, conducted in this research, assumes paramount importance.