Author
Listed:
- Kentaro Tsukamoto
(Fujita Health University School of Medicine)
- Naoaki Shinzawa
(Osaka University
Tokyo Medical and Dental University)
- Akito Kawai
(Fujita Health University School of Medicine)
- Masahiro Suzuki
(Fujita Health University School of Medicine)
- Hiroyasu Kidoya
(Osaka University)
- Nobuyuki Takakura
(Osaka University)
- Hisateru Yamaguchi
(Fujita Health University
Yokkaichi Nursing and Medical Care University)
- Toshiki Kameyama
(Fujita Health University
Fujita Health University School of Medicine)
- Hidehito Inagaki
(Fujita Health University
Fujita Health University)
- Hiroki Kurahashi
(Fujita Health University
Fujita Health University)
- Yasuhiko Horiguchi
(Osaka University)
- Yohei Doi
(Fujita Health University School of Medicine
University of Pittsburgh School of Medicine)
Abstract
Pathogenic bacteria of the genus Bartonella can induce vasoproliferative lesions during infection. The underlying mechanisms are unclear, but involve secretion of an unidentified mitogenic factor. Here, we use functional transposon-mutant screening in Bartonella henselae to identify such factor as a pro-angiogenic autotransporter, called BafA. The passenger domain of BafA induces cell proliferation, tube formation and sprouting of microvessels, and drives angiogenesis in mice. BafA interacts with vascular endothelial growth factor (VEGF) receptor-2 and activates the downstream signaling pathway, suggesting that BafA functions as a VEGF analog. A BafA homolog from a related pathogen, Bartonella quintana, is also functional. Our work unveils the mechanistic basis of vasoproliferative lesions observed in bartonellosis, and we propose BafA as a key pathogenic factor contributing to bacterial spread and host adaptation.
Suggested Citation
Kentaro Tsukamoto & Naoaki Shinzawa & Akito Kawai & Masahiro Suzuki & Hiroyasu Kidoya & Nobuyuki Takakura & Hisateru Yamaguchi & Toshiki Kameyama & Hidehito Inagaki & Hiroki Kurahashi & Yasuhiko Horig, 2020.
"The Bartonella autotransporter BafA activates the host VEGF pathway to drive angiogenesis,"
Nature Communications, Nature, vol. 11(1), pages 1-14, December.
Handle:
RePEc:nat:natcom:v:11:y:2020:i:1:d:10.1038_s41467-020-17391-2
DOI: 10.1038/s41467-020-17391-2
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