生物
致病性
载体(分子生物学)
地图集(解剖学)
致病岛
计算生物学
病毒学
微生物学
遗传学
毒力
重组DNA
基因
解剖
作者
Thomas Hart,Nicole Sonnert,Xiao‐Tian 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,Maria Tays Mendes,Agustín Rolandelli,Pallavi Singh,Abhai K. Tripathi,Choukri Ben Mamoun,Melissa J. Caimano
出处
期刊:Cell
[Cell Press]
日期:2024-06-13
卷期号:187 (15): 4113-4127.e13
被引量:10
标识
DOI:10.1016/j.cell.2024.05.023
摘要
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.
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