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JoVE Journal
Immunology and Infection
細菌や真菌によってウイルス感染細胞上のバイオフィルムの開始の決意
細菌や真菌によってウイルス感染細胞上のバイオフィルムの開始の決意
JoVE Journal
Immunology and Infection
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JoVE Journal Immunology and Infection
Determination of Biofilm Initiation on Virus-infected Cells by Bacteria and Fungi

細菌や真菌によってウイルス感染細胞上のバイオフィルムの開始の決意

Full Text
10,076 Views
12:33 min
July 6, 2016

DOI: 10.3791/54162-v

Balbina J. Plotkin1, Ira M. Sigar1, Vaibhav Tiwari1, Scott Halkyard1

1Department of Microbiology and Immunology,Midwestern University

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Please note that some of the translations on this page are AI generated. Click here for the English version.

Overview

This article describes a method for assessing the competition between bacterial and fungal pathogens for adherence to virus-infected HeLa cell monolayers. The technique allows for the examination of interactions among various prokaryotes, eukaryotes, and viruses.

Key Study Components

Area of Science

  • Microbiology
  • Virology
  • Cell Biology

Background

  • Chronic viral infections can influence the host microbiome.
  • Opportunistic pathogens like Staphylococcus aureus and Candida albicans can attach to infected cells.
  • Understanding these interactions is crucial for controlling microbial colonization.
  • HSV infection is common in the human population, affecting microbial dynamics.

Purpose of Study

  • To measure the effects of HSV-infected cells on the attachment of opportunistic pathogens.
  • To explore the role of chronic viral infections in microbiome regulation.
  • To provide insights into controlling microbial attachment in infected individuals.

Methods Used

  • Assessment of HSV1 or HSV2 virus viability and multiplicity of infection (MOI).
  • Utilization of x-gal staining for experimental assays.
  • Application of a reporter virus entry assay.
  • Evaluation of microbial attachment to virus-infected cell monolayers.

Main Results

  • The method allows quantification of pathogen adherence to infected cells.
  • Insights into the interaction dynamics between viruses and opportunistic pathogens.
  • Potential applications for understanding other viral infections like CMV and adenovirus.
  • Relevance to public health due to the prevalence of HSV in the population.

Conclusions

  • This technique provides a framework for studying microbial interactions in the context of viral infections.
  • It highlights the importance of viral infections in regulating microbial communities.
  • Future research can expand on these findings to develop strategies for controlling opportunistic pathogens.

Frequently Asked Questions

What is the main goal of this study?
The main goal is to measure the effects of HSV-infected cells on the attachment of bacterial and fungal pathogens.
How does HSV infection influence microbial attachment?
HSV infection can alter the dynamics of microbial adherence, affecting the host microbiome.
What pathogens are studied in this method?
The study focuses on Staphylococcus aureus and Candida albicans as opportunistic pathogens.
Can this method be applied to other viruses?
Yes, it can also be applied to study CMV and adenovirus infections.
What is the significance of understanding these interactions?
Understanding these interactions can help in developing strategies to control opportunistic infections in individuals with chronic viral infections.

ウイルス感染HeLa細胞単層への付着に対する王国間の関連性と競争(細菌および真菌)を決定するための方法がここに記載されています。このプロトコルは、原核生物、真核生物、およびウイルスの複数の組み合わせに拡張できます。

この実験の全体的な目標は、HSVに事前に感染した細胞が、黄色ブドウ球菌やカンジダアルビカンスなどの細菌および真菌の日和見病原体のその後の付着に及ぼす影響を測定することです。この方法は、慢性ウイルス感染が宿主マイクロバイオームのそれぞれのメンバーの調節に果たす役割に関する重要な質問に答えるのに役立ちます。この手法の主な利点は、バイオフィルム形成の開始ステップ、つまり接着性について、複数の生物の相互作用を調査および定量化できることです。

この技術の意味は、無症候性の排出を伴うHSV感染の前提条件がヒト集団の大部分に存在するため、日和見病原体のコロニー形成の制御にまで及びます。この方法は、その後の微生物付着のHSV制御に関する洞察を提供しますが、CMV感染やアデノウイルス感染などの他のシステムにも適用できます。まず、レポーターウイルスエントリーアッセイを使用して、各実験アッセイの実行について、HSV1またはHSV2ウイルスの生存率と感染の多様性、またはMOIをx-gal染色で決定します。

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