Molecular Mechanisms of Borrelia burgdorferi Phagocytosis and Intracellular Processing by Human Macrophages

被引:10
|
作者
Woitzik, Philipp [1 ]
Linder, Stefan [1 ]
机构
[1] Univ Med Ctr Eppendorf, Inst Med Microbiol Virol & Hyg, D-20246 Hamburg, Germany
来源
BIOLOGY-BASEL | 2021年 / 10卷 / 07期
关键词
Borrelia; coiling pseudopod; filopodia; Lyme disease; macrophages; phagosome; phagocytosis; T-CELL RESPONSES; LYME-DISEASE; COILING PHAGOCYTOSIS; PHAGOSOME MATURATION; COMPLEMENT RECEPTOR-3; ACTIN CYTOSKELETON; MOUSE FORMIN; HOST-DEFENSE; SENSU-LATO; IFN-GAMMA;
D O I
10.3390/biology10070567
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Simple Summary Borreliae are a group of highly motile bacteria that are characterized by their corkscrew-like shape. They can be transferred by a tick bite to a human host and cause severe illnesses. Accordingly, an untreated infection with Borrelia burgdorferi can lead to the development of Lyme disease, which can affect the skin, joints, heart and nervous system. It is thus important to understand how borreliae interact with the human immune system, and which mechanisms lead to their depletion in the human body. Macrophages are part of the innate immune system and among the first cells that encounter invading borreliae. In this review, we discuss the molecular mechanisms that enable macrophages to recognize, take up and digest borreliae. We also point out potential ways in which borreliae might evade these mechanisms. Lyme disease is the most common vector-borne illness in North America and Europe. Its causative agents are spirochetes of the Borrelia burgdorferi sensu latu complex. Infection with borreliae can manifest in different tissues, most commonly in the skin and joints, but in severe cases also in the nervous systems and the heart. The immune response of the host is a crucial factor for preventing the development or progression of Lyme disease. Macrophages are part of the innate immune system and thus one of the first cells to encounter infecting borreliae. As professional phagocytes, they are capable of recognition, uptake, intracellular processing and final elimination of borreliae. This sequence of events involves the initial capture and internalization by actin-rich cellular protrusions, filopodia and coiling pseudopods. Uptake into phagosomes is followed by compaction of the elongated spirochetes and degradation in mature phagolysosomes. In this review, we discuss the current knowledge about the processes and molecular mechanisms involved in recognition, capturing, uptake and intracellular processing of Borrelia by human macrophages. Moreover, we highlight interactions between macrophages and other cells of the immune system during these processes and point out open questions in the intracellular processing of borreliae, which include potential escape strategies of Borrelia.
引用
收藏
页数:21
相关论文
共 50 条
  • [1] Actin-Dependent Regulation of Borrelia burgdorferi Phagocytosis by Macrophages
    Naj, Xenia
    Linder, Stefan
    ACTIN CYTOSKELETON AND BACTERIAL INFECTION, 2017, 399 : 133 - 154
  • [2] Mechanisms of Borrelia burgdorferi internalization and intracellular innate immune signaling
    Petnicki-Ocwieja, Tanja
    Kern, Aurelie
    FRONTIERS IN CELLULAR AND INFECTION MICROBIOLOGY, 2014, 4
  • [3] FIB-SEM-based analysis of Borrelia intracellular processing by human macrophages
    Klose, Matthias
    Scheungrab, Maximilian
    Luckner, Manja
    Wanner, Gerhard
    Linder, Stefan
    JOURNAL OF CELL SCIENCE, 2021, 134 (05)
  • [4] The Formins FMNL1 and mDia1 Regulate Coiling Phagocytosis of Borrelia burgdorferi by Primary Human Macrophages
    Naj, Xenia
    Hoffmann, Ann-Kathrin
    Himmel, Mirko
    Linder, Stefan
    INFECTION AND IMMUNITY, 2013, 81 (05) : 1683 - 1695
  • [5] Daam1 is a regulator of filopodia formation and phagocytic uptake of Borrelia burgdorferi by primary human macrophages
    Hoffmann, Ann-Kathrin
    Naj, Xenia
    Linder, Stefan
    FASEB JOURNAL, 2014, 28 (07) : 3075 - 3089
  • [6] Outer Surface Protein OspC Is an Antiphagocytic Factor That Protects Borrelia burgdorferi from Phagocytosis by Macrophages
    Carrasco, Sebastian E.
    Troxell, Bryan
    Yang, Youyun
    Brandt, Stephanie L.
    Li, Hongxia
    Sandusky, George E.
    Condon, Keith W.
    Serezani, C. Henrique
    Yang, X. Frank
    INFECTION AND IMMUNITY, 2015, 83 (12) : 4848 - 4860
  • [7] Macrophage mediated recognition and clearance of Borrelia burgdorferi elicits MyD88-dependent and -independent phagosomal signals that contribute to phagocytosis and inflammation
    Benjamin, Sarah J.
    Hawley, Kelly L.
    Vera-Licona, Paola
    La Vake, Carson J.
    Cervantes, Jorge L.
    Ruan, Yijun
    Radolf, Justin D.
    Salazar, Juan C.
    BMC IMMUNOLOGY, 2021, 22 (01)
  • [8] ER-Coordinated Activities of Rab22a and Rab5a Drive Phagosomal Compaction and Intracellular Processing of Borrelia burgdorferi by Macrophages
    Naj, Xenia
    Linder, Stefan
    CELL REPORTS, 2015, 12 (11): : 1816 - 1830
  • [9] Molecular characterization of a flagellar/chemotaxis operon in the spirochete Borrelia burgdorferi
    Ge, YG
    Charon, NW
    FEMS MICROBIOLOGY LETTERS, 1997, 153 (02) : 425 - 431
  • [10] Molecular adaptation of Borrelia burgdorferi in the murine host
    Liang, FT
    Nelson, FK
    Fikrig, E
    JOURNAL OF EXPERIMENTAL MEDICINE, 2002, 196 (02) : 275 - 280