The Shah Lab uses viruses and engineering principles to perturb and control biological networks. We are interested in exploring two major questions:

  1. How do flaviviruses hijack host machinery to facilitate their own replication and cause disease?
  2. Can we control these biological networks for biomedical and biotechnology applications?

We use complementary techniques of global proteomics, genetics, high-throughput sequencing, microscopy and synthetic biology to tackle these questions.

Flavivirus-host interactions

Mosquito-borne flaviviruses such as dengue virus and Zika virus are a source of emerging and re-emerging infectious diseases. We study how these viruses hijack host machinery through virus-host protein interactions to better understand their replication and develop therapeutics. We have two active areas of research on flavivirus-host interactions:

Antiviral Gene Expression Program

Cells respond to viral infections by activating the expression of antiviral genes such as interferon stimulated genes (ISGs), and viruses are continually evolving ways to evade this antiviral response. We study how flaviviruses including dengue and Zika virus hijack host gene expression machinery to inhibit the antiviral innate immune response.

Zika-associated microcephaly

Viruses have long been known to cause birth defects when fetuses are infected in utero. For example, rubella virus, and cytomegalovirus cause a range of birth defects including microcephaly, in which brain and head size is severely reduced. Viral microcephaly has received renewed attention since Zika virus emerged on a global scale in 2015. We are integrating comparative systems biology approaches with high-throughput vertebrate models to build an experimental pipeline. This will enable the rapid delineation of how Zika virus-host protein interactions lead to dysfunction of host proteins and inhibition of brain development.


Autophagy is responsible for recycling cellular components into primary biological building blocks. Autophagy can be induced by the stresses elicited during pathogen infection, and can be used to clear the cell of intracellular pathogens such as viruses. However, it has recently been demonstrated that several viruses, including dengue and Zika virus, benefit from certain aspects of autophagy for replication. This begs the question, how do these viruses selectively induce beneficial aspects of autophagy while not succumbing to its antiviral potential, and can we engineer controls that mimic or negate this selective induction of autophagy?

We study how flaviviruses hijack the autophagy network in a dynamic way. Specifically, we study how protein and genetic interactions in the autophagy network change during infection, and how these relate back to the viruses’ ability to replicate.

Engineering Biological Controls

Controlling Autophagy for Biotechnology

In addition to being induced during infections, autophagy can also be induced during nutrient deprivation and high level protein production that cells can experience in industrial settings. We use systems and synthetic biology approaches to model and engineer controls over autophagy network to improve bioreactor protein yields.