Sullivan Laboratory
The Sullivan Laboratory
Molecular, Cell, and Developmental Biology
University of California at Santa Cruz
Wolbachia Transmission

Maternal transmission of Wolbachia relies on Dynein microtubule-based transport.

Overexpression of Dynamitin (p50) causes loss of Wolbachia (small red dots, see arrow)  localization

One factor contributing to the evolutionary success of Wolbachia is its efficient maternal transmission.  We have discovered that Wolbachia are uniformly distributed throughout the germline early in oogenesis, but that during mid-oogenesis bacteria concentrate in the future oocyte, exhibiting a striking anterior localization that is distinct from mitochondria and all known axis determinants.  We demonstrated that this anterior localization requires microtubules and the minus-end motor protein complex Dynein/Dynactin.  This work is published in PLOS Pathogens (Ferree et al. 2005).  We have also discovered that in some cases, Wolbachia exhibit and distinct posterior localization in the oocyte during late oogenesis.  Experiments are currently underway to determine the cellular mechanisms involved in this localization.

Our studies provide strong evidence that Wolbachia interacts with the microtubule motor proteins Dynein.  We are very interested in identifying Wolbachia proteins involved in this interaction.  This is a difficult task given that Wolbachia cannot be cultured.  Therefore, we are collaborating with the Werren lab and TIGR and have taken a genomics approach to identify candidate Wolbachia surface proteins that will be used to prepare affinity columns for biochemical identification of Wolbachia-host protein interactions.

In addition, we are developing the reagents required to develop high-throughput approaches to identify potent small molecule Wolbachia inhibitors.  The identification of inhibitors may lead to new drugs to combat elephantiasis and river blindness.  In collaboration with Alain Debec we have established a number of stable Wolbachia-infected cell lines in which the microtubules are GFP labeled.  With these lines we are in a position to perform high-throughput fluorescent RNAi and small molecule assays for disruption of Wolbachia replication, subcellular location and survival.



This material is based upon work supported by the National Science Foundation under Grant No. 0091265.

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Last updated: December 2006