Newcastle disease virus forms inclusion bodies with features of liquid-liquid phase separation

被引:3
作者
Wang, Chongyang [1 ]
Duan, Liuyuan [1 ]
Wang, Ting [1 ]
Wang, Wenbin [2 ]
Han, Yu [1 ]
Hu, Ruochen [1 ]
Hou, Qili [1 ]
Liu, Haijin [1 ]
Wang, Juan [1 ]
Wang, Xinglong [1 ]
Xiao, Sa [1 ]
Dang, Ruyi [1 ]
Wang, Junru [3 ]
Zhang, Gaiping [1 ,4 ]
Yang, Zengqi [1 ]
机构
[1] Northwest A&F Univ, Coll Vet Med, Yangling, Peoples R China
[2] Shandong Acad Agr Sci, Poultry Inst, Jinan, Peoples R China
[3] Northwest A&F Univ, Coll Chem & Pharm, Yangling, Peoples R China
[4] Henan Acad Agr Sci, Minist Agr, Key Lab Anim Immunol, Henan Prov Key Lab Anim Immunol, Zhengzhou, Peoples R China
关键词
Newcastle disease virus; Inclusion bodies; Liquid-liquid phase separation; Nucleoprotein; Phosphoprotein; ASCITES TUMOR CELLS; NUCLEOPROTEIN;
D O I
10.1016/j.vetmic.2023.109800
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Formation of inclusion bodies (IBs) is a hallmark of infections with negative-strand RNA viruses. Although the Newcastle disease virus (NDV) IBs had been observed in the 1950s, the characteristics of NDV IBs remained largely unknown. Here, we show that NDV infection triggers the formation of IBs that contain newly synthesized viral RNA. The structures of NDV IBs, observed by electron microscopy, were not membrane-bound. Fluorescence recovery after photobleaching a region of NDV IBs occurred rapidly, and IBs were dissolved by 1,6-hexanediol treatment, demonstrating they exhibited properties consistent with liquid-liquid phase separation (LLPS). We find the nucleoprotein (NP) and phosphoprotein (P) are sufficient to generate IB-like puncta, with the N arm domain and N core region of NP and the C terminus of P playing important roles in this process. In summary, our findings suggest that NDV forms IBs containing viral RNA, and provide insights into the formation of NDV IBs.
引用
收藏
页数:8
相关论文
共 23 条
  • [2] Biomolecular condensates: organizers of cellular biochemistry
    Banani, Salman F.
    Lee, Hyun O.
    Hyman, Anthony A.
    Rosen, Michael K.
    [J]. NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2017, 18 (05) : 285 - 298
  • [4] Structure and organization of paramyxovirus particles
    Cox, Robert M.
    Plemper, Richard K.
    [J]. CURRENT OPINION IN VIROLOGY, 2017, 24 : 105 - 114
  • [5] Newcastle disease virus: Current status and our understanding
    Ganar, Ketan
    Das, Moushumee
    Sinha, Sugandha
    Kumar, Sachin
    [J]. VIRUS RESEARCH, 2014, 184 : 71 - 81
  • [6] Liquid-liquid phase separation underpins the formation of replication factories in rotaviruses
    Geiger, Florian
    Acker, Julia
    Papa, Guido
    Wang, Xinyu
    Arter, William E.
    Saar, Kadi L.
    Erkamp, Nadia A.
    Qi, Runzhang
    Bravo, Jack Pk
    Strauss, Sebastian
    Krainer, Georg
    Burrone, Oscar R.
    Jungmann, Ralf
    Knowles, Tuomas P. J.
    Engelke, Hanna
    Borodavka, Alexander
    [J]. EMBO JOURNAL, 2021, 40 (21)
  • [7] Measles virus nucleo- and phosphoproteins form liquid-like phase-separated compartments that promote nucleocapsid assembly
    Guseva, Serafima
    Milles, Sigrid
    Jensen, Malene Ringkjobing
    Salvi, Nicola
    Kleman, Jean-Philippe
    Maurin, Damien
    Ruigrok, Rob W. H.
    Blackledge, Martin
    [J]. SCIENCE ADVANCES, 2020, 6 (14)
  • [8] Phase Transitions Drive the Formation of Vesicular Stomatitis Virus Replication Compartments
    Heinrich, Bianca S.
    Maliga, Zoltan
    Stein, David A.
    Hyman, Anthony A.
    Whelan, Sean P. J.
    [J]. MBIO, 2018, 9 (05):
  • [9] Heat Shock Protein 70 Regulates Degradation of the Mumps Virus Phosphoprotein via the Ubiquitin-Proteasome Pathway
    Katoh, Hiroshi
    Kubota, Toru
    Kita, Shunsuke
    Nakatsu, Yuichiro
    Aoki, Natsuko
    Mori, Yoshio
    Maenaka, Katsumi
    Takeda, Makoto
    Kidokoro, Minoru
    [J]. JOURNAL OF VIROLOGY, 2015, 89 (06) : 3188 - 3199
  • [10] Regions on nucleocapsid protein of Newcastle disease virus that interact with its phosphoprotein
    Kho, CL
    Tan, WS
    Tey, BT
    Yusoff, K
    [J]. ARCHIVES OF VIROLOGY, 2004, 149 (05) : 997 - 1005