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An atlas of human vector-borne microbe interactions reveals pathogenicity mechanisms

  • Thomas M. Hart
  • , Nicole D. Sonnert
  • , Xiaotian Tang
  • , Reetika Chaurasia
  • , Paige E. Allen
  • , Jason R. Hunt
  • , Curtis B. Read
  • , Emily E. Johnson
  • , Gunjan Arora
  • , Yile Dai
  • , Yingjun Cui
  • , Yu Min Chuang
  • , Qian Yu
  • , M. Sayeedur Rahman
  • , M. Tays Mendes
  • , Agustin Rolandelli
  • , Pallavi Singh
  • , Abhai K. Tripathi
  • , Choukri Ben Mamoun
  • , Melissa J. Caimano
  • Justin D. Radolf, Yi Pin Lin, Volker Fingerle, Gabriele Margos, Utpal Pal, Raymond M. Johnson, Joao H.F. Pedra, Abdu F. Azad, Jeanne Salje, George Dimopoulos, Joseph M. Vinetz, Jason A. Carlyon, Noah W. Palm, Erol Fikrig, Aaron M. Ring
  • Yale University School of Medicine
  • Virginia Commonwealth University
  • Yale University
  • University of Maryland School of Medicine
  • Johns Hopkins Bloomberg School of Public Health
  • UConn Health
  • UConn Health
  • Wadsworth Center for Laboratories and Research
  • Bavarian Health and Food Safety Authority
  • University of Maryland, College Park
  • University of Cambridge
  • Fred Hutchinson Cancer Research Center

Producción científica: Contribución a una revistaArtículorevisión exhaustiva

16 Citas (Scopus)

Resumen

Vector-borne diseases are a leading cause of death worldwide and pose a substantial unmet medical need. Pathogens binding to host extracellular proteins (the “exoproteome”) represents a crucial interface in the etiology of vector-borne disease. Here, we used bacterial selection to elucidate host-microbe interactions in high throughput (BASEHIT)—a technique enabling interrogation of microbial interactions with 3,324 human exoproteins—to profile the interactomes of 82 human-pathogen samples, including 30 strains of arthropod-borne pathogens and 8 strains of related non-vector-borne pathogens. The resulting atlas revealed 1,303 putative interactions, including hundreds of pairings with potential roles in pathogenesis, including cell invasion, tissue colonization, immune evasion, and host sensing. Subsequent functional investigations uncovered that Lyme disease spirochetes recognize epidermal growth factor as an environmental cue of transcriptional regulation and that conserved interactions between intracellular pathogens and thioredoxins facilitate cell invasion. In summary, this interactome atlas provides molecular-level insights into microbial pathogenesis and reveals potential host-directed targets for next-generation therapeutics.

Idioma originalInglés
Páginas (desde-hasta)4113-4127.e13
PublicaciónCell
Volumen187
N.º15
DOI
EstadoPublicada - 25 jul. 2024

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