Robert J Bastidas

Robert J Bastidas
  • PhD. Genetics and Genomics
  • Professor (Assistant) at Duke University

About

72
Publications
12,297
Reads
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2,295
Citations
Introduction
I am a microbiologist working on host-pathogen interactions. I use microscopy, proteomics, genomics, molecular biology, biochemistry, and high-throughput assays to understand how bacterial pathogens survive inside human cells and pattern immune responses.
Current institution
Duke University
Current position
  • Professor (Assistant)
Additional affiliations
January 2010 - January 2014
Duke University Medical Center
Position
  • PostDoc Position
May 2009 - January 2010
Duke University
Position
  • Researcher
Description
  • Elucidated mechanisms by which the small compound rapamycin exerts its antimicrobial activity on fungal human pathogens
August 2003 - May 2009
Duke University
Position
  • PhD Student
Education
January 2003 - January 2009
Duke University
Field of study
  • Microbiology

Publications

Publications (72)
Article
Full-text available
Many cellular processes are regulated by ubiquitin-mediated proteasomal degradation. Pathogens can regulate eukaryotic proteolysis through the delivery of proteins with de-ubiquitinating (DUB) activities. The obligate intracellular pathogen Chlamydia trachomatis secretes Cdu1 (ChlaDUB1), a dual deubiquitinase and Lys-acetyltransferase, that promote...
Preprint
Many cellular processes are regulated by ubiquitin-mediated proteasomal degradation. Pathogens can regulate eukaryotic proteolysis through the delivery of proteins with de-ubiquitinating (DUB) activities. The obligate intracellular pathogen Chlamydia trachomatis secretes Cdu1 (ChlaDUB1), a dual deubiquitinase and Lys-acetyltransferase, that promote...
Article
Chlamydia trachomatis (Ct) is an intracellular bacterial pathogen that relies on the activity of secreted proteins known as effectors to promote replication and avoidance of immune clearance. Understanding the contribution of Ct effectors to pathogenesis has proven to be challenging, given that these proteins often perform multiple functions during...
Preprint
Full-text available
Many cellular processes are regulated by ubiquitin-mediated proteasomal degradation. Bacterial pathogens can regulate eukaryotic proteolysis through the delivery of proteins with de-ubiquitinating (DUB) activities. The obligate intracellular pathogen Chlamydia trachomatis secretes Cdu1 (ChlaDUB1), a dual deubiquitinase and Lys-acetyltransferase, th...
Preprint
Many cellular processes are regulated by ubiquitin-mediated proteasomal degradation. Bacterial pathogens can regulate eukaryotic proteolysis through the delivery of proteins with de-ubiquitinating (DUB) activities. The obligate intracellular pathogen Chlamydia trachomatis secretes Cdu1 (ChlaDUB1), a dual deubiquitinase and Lys-acetyltransferase, th...
Preprint
Full-text available
Many cellular processes are regulated by ubiquitin-mediated proteasomal degradation. Bacterial pathogens can regulate eukaryotic proteolysis through the delivery of proteins with de-ubiquitinating (DUB) activities. The obligate intracellular pathogen Chlamydia trachomatis secretes Cdu1 (ChlaDUB1), a dual deubiquitinase and Lys-acetyltransferase, th...
Article
Chlamydia trachomatis is the leading cause of sexually transmitted bacterial infections and a major threat to women’s reproductive health in particular. This obligate intracellular pathogen resides and replicates within a cellular compartment termed an inclusion, where it is sheltered by unknown mechanisms from gamma-interferon (IFNγ)-induced cell-...
Preprint
Chlamydia trachomatis is an obligate intracellular pathogen that replicates within a specialized membrane-bound compartment, called the inclusion. Chlamydia species express a unique class of effectors, Incs, which are translocated from the bacteria by a Type III secretion system and are inserted into the inclusion membrane where they modulate the h...
Chapter
Chlamydia is a major etiological agent of human disease that affects millions of individuals worldwide. Historically, our understanding of the mechanisms that contribute to its pathogenesis has been limited. However, the recent development of powerful genetic tools for manipulating Chlamydia has resulted in significant gains in our ability to disse...
Article
Full-text available
Chlamydia trachomatis is the most common sexually transmitted bacterial pathogen in humans and a frequent cause of asymptomatic, persistent infections leading to serious complications, particularly in young women. Chlamydia displays a unique obligate intracellular lifestyle involving the infectious elementary body and the replicative reticulate bod...
Article
Full-text available
Pathogenic bacteria are armed with potent effector proteins that subvert host signalling processes during infection¹. The activities of bacterial effectors and their associated roles within the host cell are often poorly understood, particularly for Chlamydia trachomatis², a World Health Organization designated neglected disease pathogen. We identi...
Article
Full-text available
Chlamydia has emerged as an important model system for the study of host pathogen interactions, in part due to a resurgence in the development of tools for its molecular genetic manipulation. An additional tool, published by Keb et al. (G. Keb, R. Hayman, and K. A. Fields, J. Bacteriol. 200:e00479-18, 2018, https://doi.org/10.1128/JB.00479-18), now...
Article
Full-text available
The type II fatty acid synthesis (FASII) pathway is essential for bacterial lipid biosynthesis and continues to be a promising target for novel antibacterial compounds. Recently, it has been demonstrated that Chlamydia is capable of FASII and this pathway is indispensable for Chlamydia growth. Previously, a high-content-screen was performed with C....
Article
Evading cell death is critical for Chlamydia to maintain a replicative niche, but the underlying mechanisms are unknown. We screened a library of Chlamydia mutants for modulators of cell death. Inactivation of the inclusion membrane protein CpoS (Chlamydia promoter of survival) induced rapid apoptotic and necrotic death in infected cells. The prote...
Article
Full-text available
Chlamydia species infect millions of individuals worldwide and are important etiological agents of sexually transmitted disease, infertility, and blinding trachoma. Historically, the genetic intractability of this intracellular pathogen has hindered the molecular dissection of virulence factors contributing to its pathogenesis. The obligate intrace...
Article
Full-text available
Chlamydia (C.) trachomatis is the most prevalent bacterial sexually transmitted infection worldwide and the leading cause of preventable blindness. Genetic approaches to investigate C. trachomatis have been only recently developed due to the organism’s intracellular developmental cycle. HtrA is a critical stress response serine protease and chapero...
Article
Gene inactivation by transposon insertion or allelic exchange is a powerful approach to probe gene function. Unfortunately, many microbes, including Chlamydia, are not amenable to routine molecular genetic manipulations. Here we describe an arrayed library of chemically induced mutants of the genetically intransigent pathogen Chlamydia trachomatis,...
Article
Full-text available
The intracellular bacterial pathogen Coxiella burnetii directs biogenesis of a parasitophorous vacuole (PV) that acquires host endolysosomal components. Formation of a PV that supports C. burnetii replication requires a Dot/Icm type 4B secretion system (T4BSS) that delivers bacterial effector proteins into the host cell cytosol. Thus, a subset of T...
Article
Full-text available
In a screen for compounds that inhibit infectivity of the obligate intracellular pathogen Chlamydia trachomatis, we identified the 2-pyridone amide KSK120. A fluorescent KSK120 analogue was synthesized and observed to be associated with the C. trachomatis surface, suggesting that its target is bacterial. We isolated KSK120-resistant strains and det...
Article
Full-text available
Microorganisms evolve via a range of mechanisms that may include or involve sexual/parasexual reproduction, mutators, aneuploidy, Hsp90 and even prions. Mechanisms that may seem detrimental can be repurposed to generate diversity. Here we show that the human fungal pathogen Mucor circinelloides develops spontaneous resistance to the antifungal drug...
Article
Full-text available
The secreted Chlamydia protease CPAF cleaves a defined set of mammalian and Chlamydia proteins in vitro. As a result, this protease has been proposed to modulate a range of bacterial and host cellular functions. However, it has recently come into question the extent to which many of its identified substrates constitute bona fide targets of proteoly...
Article
Full-text available
Chlamydia trachomatis, the causative agent of trachoma and sexually transmitted infections, employs a type III secretion (T3S) system to deliver effector proteins into host epithelial cells to establish a replicative vacuole. Aside from the phosphoprotein TARP, a Chlamydia effector that promotes actin re-arrangements, very few factors mediating bac...
Article
Full-text available
Salicylidene acylhydrazides (SAHs) inhibit the type III secretion system (T3S) of Yersinia and other Gram-negative bacteria. In addition, SAHs restrict the growth and development of Chlamydia species. However, since the inhibition of Chlamydia growth by SAH is suppressed by the addition of excess iron and since SAHs have an iron-chelating capacity,...
Article
Full-text available
Chlamydia trachomatis is the most common sexually transmitted bacterial pathogen and the causative agent of blinding trachoma. Although Chlamydia is protected from humoral immune responses by residing within remodeled intracellular vacuoles, it still must contend with multilayered intracellular innate immune defenses deployed by its host while scav...
Article
Full-text available
The zygomycete Mucor circinelloides is an opportunistic fungal pathogen that commonly infects patients with malignancies, diabetes mellitus, and solid organ transplants. Despite the widespread use of antifungal therapy in the management of zygomycosis, the incidence of infections continues to rise among immunocompromised individuals. In this study,...
Article
The rapamycin-sensitive TORC1 protein kinase is the central component of a conserved signal transduction cascade controlling cell growth in response to nutrients and growth factors. Groundbreaking studies are uncovering novel roles for the endomembrane vesicular trafficking system as a platform for TORC1 signaling. TORC1 components, regulators, and...
Article
Full-text available
The nutrient-sensing Tor pathway governs cell growth and is conserved in nearly all eukaryotic organisms from unicellular yeasts to multicellular organisms, including humans. Tor is the target of the immunosuppressive drug rapamycin, which in complex with the prolyl isomerase FKBP12 inhibits Tor functions. Rapamycin is a gold standard drug for orga...
Data
supplemental Table 1 - Accession numbers of putative Tor pathway components. Putative Tor pathway components were assigned using reciprocal best hit BLAST matches with the following public databases: S. cerevisiae, SGD, http://www.yeastgenome.org; S. pombe, GeneDB, http://www.genedb.org/genedb/pombe/index.jsp; P. ostreatus, JGI, http://genome.jgi-p...
Data
supplemental Figure 1 - Syntenic conservation of genomic area surrounding TOR1 and TOR2 in Candida glabrata. The top bar represents C. glabrata chromosome F and the bottom bar represents C. glabrata chromosome K. On chromosome F, the first five genes correspond to CAGL0F00110g, CAGL0F00121g, CAGL0F00143g, CAGL0F00154g, and CAGL0F00165g. Red lines i...
Data
supplemental figure 2 - There is no syntenic conservation in Schizosaccharomyces species surrounding the TOR genomic regions. Red lines indicate syntenic genes oriented in the same direction whereas blue lines indicate syntenic genes oriented in the opposite direction (i.e., + strand and - strand). No syntenic conservation was observed in the separ...
Article
Full-text available
Eukaryotic cell growth is coordinated in response to nutrient availability, growth factors, and environmental stimuli, enabling cell-cell interactions that promote survival. The rapamycin-sensitive Tor1 protein kinase, which is conserved from yeasts to humans, participates in a signaling pathway central to cellular nutrient responses. To gain insig...
Data
Upregulated genes induced by rapamycin treatment of wild type (SC5314) cells during growth in YPD at 30°C (0.15 MB DOC)
Data
Differentially expressed genes induced by rapamycin treatment of a TOR1-1/TOR1 (RapaR) strain grown in YPD at 30°C (0.10 MB DOC)
Data
Rapamycin induces cellular aggregation of Candida guilliermondii cells. (A) Wild type (ATCC 6260) cell culture suspensions grown in liquid Spider medium flocculate in the presence of 20 nM rapamycin after 2 hours of incubation at 37°C. (B) Microscopic images of wild type cell cultures shown in (A) at 0 and 3 hours of rapamycin treatment. Results sh...
Data
Strains used in this study (0.10 MB DOC)
Data
Primers used for northern probe amplification (0.06 MB DOC)
Data
Upregulated gene expression after rapamycin treatment of wild type cells grown in Spider liquid medium for 90 minutes at 37°C (0.26 MB DOC)
Article
Full-text available
The fungal kingdom encompasses ≈1.5 million species (1) as diverse as single-celled yeasts, pathogens of animals/plants, and plant root symbionts. Fungi are eukaryotic, closely aligned with metazoans (2, 3). Animals and fungi diverged ≈1 billion years ago; their last common ancestor was unicellular, motile, and aquatic. Some fungi grow as unicellul...
Article
Full-text available
Microbes evolved to produce natural products that inhibit growth of competing soil microorganisms. In many cases these compounds act on fungi, which are eukaryotes with conserved gene sequences closely related to metazoans, including humans. The calcineurin inhibitors cyclosporin A and FK-506, the Tor inhibitor rapamycin, and the Hsp90 inhibitor ge...
Article
The yeast Saccharomyces cerevisiae senses and responds to nutrients by adapting its growth rate and undergoing morphogenic transitions to ensure survival. The Tor pathway is a major integrator of nutrient-derived signals that in coordination with other signaling pathways orchestrates cell growth. Recent advances have identified novel Tor kinase sub...
Article
The Second FEBS Advanced Lecture Course on Human Fungal Pathogens: Molecular Mechanisms of Host-Pathogen Interactions and Virulence, organized by Christophe d'Enfert (Institut Pasteur, France), Anita Sil (UCSF, USA), and Steffen Rupp (Fraunhofer, IGB, Germany), occurred May 2007 in La Colle sur Loup, France. Here we review the advances presented an...
Article
Inositol pyrophosphates are a diverse group of high-energy signaling molecules whose cellular roles remain an active area of study. We report a previously uncharacterized class of inositol pyrophosphate synthase and find it is identical to yeast Vip1 and Asp1 proteins, regulators of actin-related protein-2/3 (ARP 2/3) complexes. Vip1 and Asp1 acted...
Article
Full-text available
Phytate (inositol hexakisphosphate, IP6) is a regulator of intracellular signaling, a highly abundant animal antinutrient, and a phosphate store in plant seeds. Here, we report a requirement for inositol polyphosphate kinases, AtIPK1 and AtIPK2β, for the later steps of phytate synthesis in Arabidopsis thaliana. Coincident disruption of these kinase...
Article
Full-text available
The production of inositol polyphosphate (IPs) and pyrophosphates (PP-IPs) from inositol 1,4,5-trisphosphate (I(1,4,5)P3) requires the 6-/3-/5-kinase activity of Ipk2 (also known as Arg82 and inositol polyphosphate multikinase). Here, we probed the distinct roles for I(1,4,5)P3 6- versus 3-kinase activities in IP metabolism and cellular functions r...
Article
Fungal cells sense the amount and quality of external nutrients through multiple interconnected signaling networks, which allow them to adjust their metabolism, transcriptional profiles and developmental programs to adapt readily and appropriately to changing nutritional states. In organisms ranging from yeasts to humans, the Tor signaling pathway...

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I am interested in synthesizing the gene coding for this transposase but can't find the sequence.

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