The HopQ-CEACAM Interaction Controls CagA Translocation, Phosphorylation, and Phagocytosis of <i>Helicobacter pylori</i> in Neutrophils
Ina‐Kristin Behrens, Benjamin Busch, Hellen Ishikawa‐Ankerhold, Pia Palamides, John E. Shively, Cliff Stanners, Carlos H.F. Chan, Nelly Leung, Scott D. Gray‐Owen, Rainer Haas
Abstract
Helicobacter pylori is highly adapted to humans and evades host immunity to allow its lifelong colonization. However, the H. pylori mouse model is artificial for H. pylori , and few adapted strains allow gastric colonization. Here, we show that human or CEACAM-humanized, but not mouse neutrophils are manipulated by the H. pylori HopQ-CEACAM interaction. Human CEACAMs are responsible for CagA phosphorylation, activation, and processing in neutrophils, whereas CagA translocation and tyrosine phosphorylation in DCs and macrophages is independent of the HopQ-CEACAM interaction. H. pylori affects the secretion of distinct chemokines in CEACAM-humanized neutrophils and macrophages. Most importantly, human CEACAMs on neutrophils enhance binding, oxidative burst, and phagocytosis of H. pylori and enhance bacterial survival in the phagosome. The H. pylori -CEACAM interaction modulates PMNs to reduce the H. pylori CagA translocation efficiency in vivo and to fine-tune the expression of CEACAM receptors on neutrophils to limit translocation of CagA and gastric pathology.