Autophagy-associated dengue vesicles promote viral transmission avoiding antibody neutralization

نویسندگان

  • Yan-Wei Wu
  • Clément Mettling
  • Shang-Rung Wu
  • Chia-Yi Yu
  • Guey-Chuen Perng
  • Yee-Shin Lin
  • Yea-Lih Lin
چکیده

One of the major defense mechanisms against virus spread in vivo is the blocking of viral infectibility by neutralizing antibodies. We describe here the identification of infectious autophagy-associated dengue vesicles released from infected cells. These vesicles contain viral proteins E, NS1, prM/M, and viral RNA, as well as host lipid droplets and LC3-II, an autophagy marker. The viral RNA can be protected within the autophagic organelles since anti-dengue neutralizing antibodies do not have an effect on the vesicle-mediated transmission that is able to initiate a new round of infection in target cells. Importantly, such infectious vesicles were also detected in a patient serum. Our study suggests that autophagy machinery plays a new role in dengue virus transmission. This discovery explains the inefficiency of neutralizing antibody upon dengue infection as a potential immune evasion mechanism in vivo.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Autophagy Facilitates Antibody-Enhanced Dengue Virus Infection in Human Pre-Basophil/Mast Cells

BACKGROUND Dengue virus (DENV) infection can cause severe hemorrhagic disease in humans. Although the pathogenic mechanisms underlying severe DENV disease remain unclear, one of the possible contributing factors is antibody-dependent enhancement (ADE) which occurs when sub-neutralizing antibodies derived from a previous DENV infection enhance viral infection through interaction between virus-an...

متن کامل

Cross-reacting antibodies enhance dengue virus infection in humans.

Dengue virus co-circulates as four serotypes, and sequential infections with more than one serotype are common. One hypothesis for the increased severity seen in secondary infections is antibody-dependent enhancement (ADE) leading to increased replication in Fc receptor-bearing cells. In this study, we have generated a panel of human monoclonal antibodies to dengue virus. Antibodies to the stru...

متن کامل

Dengue vaccine development and dengue viral neutralization and enhancement assays.

Dengue fever is a major tropical infectious disease that affects 50-100 million people each year. Its complications, namely dengue haemorrhagic fever and dengue shock syndrome, disproportionately afflict children and young adults. The primary goal of several vaccines now in development is to elicit protective neutralizing antibody responses; however, the exact definition of such responses remai...

متن کامل

Detection of Dengue Viral Rna in Mosquitoes (aedes Sp.) by Nucleic Acid Sequence-based Amplification (nasba) and Reverse Transcriptase-polymerase Chain Reaction (rt-pcr)

of the Joint International Tropical Medicine Meeting (JITMM). Bangkok, Thailand. 29 November-1 December 2004:106. EVALUATION OF A SINGLE-DILUTION PLAQUE REDUCTION NEUTRALIZATION TEST (PRNT) AS A DIAGNOSTIC TOOL FOR DETECTING INTERCURRENT DENGUE VIRUS (DENV) INFECTIONS Thomas SJ, Nisalak A, Halstead S, Endy T, Lutthiwongsakorn N, Poolpanichupatam Y, Sawatwong P, Changnak S and Mammen MP Jr Studi...

متن کامل

Mechanisms of immune evasion induced by a complex of dengue virus and preexisting enhancing antibodies.

We have found that dengue virus (DENV) not only uses preexisting enhancing antibodies to promote its entry into Fc receptor-bearing cells but also exploits enhancing antibodies for intracellular immune evasion through 2 mechanisms. In the first mechanism, entry of DENV-antibody complexes into human monocytic cells activates negative regulators, dihydroxyacetone kinase and autophagy-related 5-au...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره 6  شماره 

صفحات  -

تاریخ انتشار 2016