Organoids: A New Cell Technology Model to Understand Zika Virus Induced Microcephaly | OMICS International
Journal of Infectious Disease and Pathology

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Organoids: A New Cell Technology Model to Understand Zika Virus Induced Microcephaly

Viroj Wiwanitkit*

Professor, Surindra Rajabhat University, Thailand

*Corresponding Author:
Viroj Wiwanitkit
Professor, Senior Expert, Surindra Rajabhat University, Thailand
Tel: 6624132436
E-mail: [email protected]

Received date: April 07, 2017; Accepted date: April 08, 2017; Published date: April 15, 2017

Citation: Wiwanitkit V (2017) Organoids: A New Cell Technology Model to Understand Zika Virus Induced Microcephaly. J Emerg Infect Dis 2:e003. doi: 10.4172/2472-4998.1000e003

Copyright: © 2017 Wiwanitkit V. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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The Zika virus (ZIKV) infection is the present big problem. As a vector borne disease, this infection becomes a problem in several tropical areas around the world. The great concern is the possibility that the transplacental transmission of the pathogen can result in microcephaly child [1]. To understand the pathophysiology of microcephaly due to ZIKV infection is a very interesting topic. Adding to the report by Sakkas et al. [1], the new technology for understanding the pathophysiology of ZIKV infection should also be mentioned. In fact, there are many reports on histopathology and molecular pathology of the ZIKV virus infected cases with microcephaly [2,3]. Nevertheless, those works do not reflect the developmental pathology. The use of animal models might be partial useful, however, it cannot represent the exact process in human beings [4]. To study the developmental pathology, the use of the advanced cell technology, organoids is an interesting alternative technique. The use of brain organoids for understanding ZIKV induced microcephaly is an interesting approach. Qian et al. recently discussed “perspectives on overcoming limitations of current organoid systems for their future use in ZIKV research [5].” In fact, organoids is the new cell technology that is proposed for its advantage in assessment of pathophysiology of many medical disorders. The use for clarification on the pathogenesis of ZIKV infection is also proposed in the medical literature. Nevertheless, there are many limitations of using organoids at present. The usefulness of using organoids technology as a way to assess the pathogenesis of ZIKV induced microcephaly can be expected. Nevertheless, there should be a balanced discussion of the topic-including highlighting some of the limitations with using organoid models to understand ZIKV.

The important concern is lack for the ability to assess or model the complete immunopathogenesis that might related to the ZIKV induced microcephaly. To assess the additional role of immunopathogenesis, the actual animal model is still also needed [6]. In addition, the ogranoids model might not be able to answer the epidemiological difference of ZIKV induced microcephaly in tropical America and Asia. The effect of genetic and epigenetic relating to each setting cannot be assessed by organoids study. Although organoids might clarify the pathological effect of ZIKV, it is no doubt that there will not be a final proof for the case of microcephaly since the organoids cannot be able to finally develop to the overt phenotype of microcephaly. Finally, the adverse or unwanted effect of organoids model is the topic that should not be forgoten. There is still no proof on the safety of the technology and there is a need to verify whether there is any environmental toxicology effect of the organoids model. This is a big ethical issue for this new technology [7].

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