Establishing Mouse Models for Zika Virus-induced Neurological Disorders Using Intracerebral Injection Strategies: Embryonic, Neonatal, and Adult

Stephanie A. Herrlinger; Qiang Shao; Li Ma; Melinda Brindley; Jian-Fu Chen

doi:10.3791/56486

Mausmodelle für Zika-Virus-induzierte neurologische Erkrankungen mit intrazerebrale Injektion Str...

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Establishing Mouse Models for Zika Virus-induced Neurological Disorders Using Intracerebral Injection Strategies: Embryonic, Neonatal, and Adult

Mausmodelle für Zika-Virus-induzierte neurologische Erkrankungen mit intrazerebrale Injektion Strategien etablieren: embryonale, Neugeborene und Erwachsene

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09:39 min

April 26, 2018

DOI: 10.3791/56486-v

Stephanie A. Herrlinger¹, Qiang Shao², Li Ma², Melinda Brindley³, Jian-Fu Chen²

¹Biomedical and Health Sciences Institute,University of Georgia, ²Center for Craniofacial Molecular Biology,University of Southern California, ³Department of Infectious Diseases, College of Veterinary Medicine,University of Georgia

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Overview

This study presents a method for creating in vivo models of Zika virus infection in the brain using a mouse model. The primary focus is on understanding the pathology and mechanisms of Zika virus-induced microcephaly at various developmental stages, which has implications for therapies and diagnostics.

Key Study Components

Area of Science

Neuroscience
Virology
In vivo models

Background

Zika virus infection is linked to microcephaly in fetuses.
Understanding viral mechanics in the brain is crucial for addressing neurodevelopmental disorders.
This technique can also extend to other flavivirus infections, like dengue.

Purpose of Study

To establish a reliable method for studying Zika virus infections in the brain.
To investigate the effects of the virus at embryonic, neonatal, and adult stages.
To explore implications for therapy and diagnosis of associated disorders.

Methods Used

A surgical method for intracerebral inoculation of Zika virus in mouse models.
The primary biological model involves injecting embryos, neonatal pups, and adult mice.
Important steps include preparing injection syringes, anesthetizing subjects, and injecting Zika virus into specified brain regions.
Monitoring recovery and ensuring sterile conditions during surgical procedures are emphasized.

Main Results

The technique allows for controlled infection of the brain, facilitating detailed study of viral pathogenesis.
Significant insights into the development of neurodevelopmental issues related to Zika infection are anticipated.
Potentially applicable to other flavivirus models enhances the method's versatility.

Conclusions

This study establishes a foundational protocol for investigating Zika virus impact on brain development.
Insights gained may enable advancements in understanding and treating Zika-related disorders.

Frequently Asked Questions

What are the advantages of this model for studying Zika virus?

The model allows precise control of viral inoculation in various developmental stages and can yield insights into the pathology of Zika virus infections.

How is the biological model implemented?

The model involves injecting Zika virus into the brains of embryos, neonatal pups, or adult mice to study the disease's progression and effects.

What types of data are obtained from this method?

Data obtained may include viral load, developmental outcomes, and neurodevelopmental changes associated with Zika infection.

What are the limitations of this method?

Considerations include the invasive nature of the procedure and ensuring anesthetic adequacy during surgery to minimize risks to the animals.

How can this technique be adapted for other infections?

By modifying virus strains used or adjusting injection protocols, this method can be adapted to study other flavivirus infections, such as dengue.

What is the significance of studying Zika virus in the brain?

Understanding the viral mechanisms in the brain is crucial for developing interventions to address microcephaly and other neurodevelopmental issues associated with infection.

Hier beschreiben wir eine Methode für den Aufbau eines Modells von Zika virusbedingte Mikrozephalie in Maus. Dieses Protokoll enthält Methoden zum embryonalen, Neugeborenen und Erwachsenen-Bühne intrazerebrale Inokulation von Zika-Virus.

Das übergeordnete Ziel der hier vorgestellten Operationsmethoden ist es, in vivo Modelle der intrakraniellen Zika-Virusinfektion zu etablieren. Diese Methode kann dazu beitragen, die Schlüsselfragen auf diesem Gebiet zu beantworten, wie z. B. die Pathologie und den Mechanismus der Zika-Virusinfektion im Gehirn sowohl im frühen und späteren Entwicklungsstadium als auch im Erwachsenenstadium. Der Hauptvorteil dieser Technik besteht darin, dass die Richtungsinfektion des Gehirns leicht erreicht werden kann.

Die Implikationen dieser Technik erstrecken sich auf Therapien oder Diagnosen von Zika-Virus-induzierter Mikrozephalie oder anderen neurologischen Entwicklungsstörungen. Obwohl diese Methode einen Einblick in die Pathogenese des Zika-Virus geben kann, kann sie auch zur Untersuchung anderer Flavivirus-Infektionen im Gehirn, wie z. B. des Dengue-Virus, angewendet werden. Laden Sie kurz vor der Operation die Zika-Virus-Injektionsmischung in eine vorbereitete Glasinjektionsnadel, indem Sie zuerst die gasdichte 50-Mikroliter-Injektionsspritze, den Luer-Lock-Aufsatz und den Schlauch zusammenfügen.

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