Treponema pallidum subsp. pallidum genetic population structure and relevance to syphilis prevention and treatment.
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Aghakhanian Farhang, Lieberman Nicole A P, Hennelly Christopher M, Chen Jane S, Bettin Everton B, Nunley B Ethan, Chen Wentao, Yang Ligang, Matoga Mitch, Hoffman Irving F, Altcheh Jaime M, Garcia Luciana Noemí, Rabinovich Andrés, Pardal Patricia Fernández, Leiro Viviana, Manathunge Ariyaratne K A, Elwitigala Jayanthi P, Lukehart Sheila A, Hook Edward W, Leal Passos Mauro Romero, Campos Arze Wilma Nancy, Andrade Hugo Boechat, Mulcahy Fiona, Wang Qian-Qiu, Zhang Rui-Li, Kou Cai-Xia, Vargas Silver K, Konda Kelika A, Diaz Michael Reyes, Ha Tran Veit, Doanh Le Huu, Nakayama Shu-Ichi, Ohama Yuki, Ohnishi Makoto, Yang Bin, Šmajs David, Pospíšilová Petra, Caimano Melissa J, Juliano Jonathan J, Moody M Anthony, Salazar Juan C, Radolf Justin D, Nadal-Barón Patricia, Xu Linda H, Giacani Lorenzo, Hawley Kelly L, Greninger Alexander L, Seña Arlene C, Parr Jonathan B
Аннотация
SIGNIFICANCE STATEMENT: Despite increasing syphilis rates worldwide, genomic data from its causative agent Treponema pallidum subsp. pallidum have largely originated from a small number of high-income countries. This study significantly expands our understanding of TPA genomic diversity by sampling across underrepresented low- and middle-income countries (LMICs) in Africa, Asia and South America. We analyze 1,707 genomes, including 298 newly sequenced from 11 LIMCs, and identify novel subpopulations, lineage-specific variation in outer membrane proteins, and geographic differences in antimicrobial resistance markers. These results illustrate how sampling from understudied regions reveals previously unappreciated, geographically structured diversity, improving our understanding of TPA population structure and informing the development of globally relevant vaccines, treatment strategies, and diagnostic tools.