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1.
J Gen Virol ; 99(5): 743-752, 2018 05.
Article in English | MEDLINE | ID: mdl-29616892

ABSTRACT

The ability of the matrix (M) protein of potato yellow dwarf virus (PYDV) to remodel nuclear membranes is controlled by a di-leucine motif located at residues 223 and 224 of its primary structure. This function can be uncoupled from that of its nuclear localization signal (NLS), which is controlled primarily by lysine and arginine residues immediately downstream of the LL motif. In planta localization of green fluorescent protein fusions, bimolecular fluorescence complementation assays with nuclear import receptor importin-α1 and yeast-based nuclear import assays provided three independent experimental approaches to validate the authenticity of the M-NLS. The carboxy terminus of M is predicted to contain a nuclear export signal, which is belived to be functional, given the ability of M to bind the Arabidopsis nuclear export receptor 1 (XPO1). The nuclear shuttle activity of M has implications for the cell-to-cell movement of PYDV nucleocapsids, based upon its interaction with the N and Y proteins.


Subject(s)
Nuclear Localization Signals/genetics , Rhabdoviridae/genetics , Viral Matrix Proteins/genetics , Active Transport, Cell Nucleus , Arabidopsis/genetics , Arabidopsis/metabolism , Arabidopsis Proteins/genetics , Arabidopsis Proteins/metabolism , Cell Nucleus/metabolism , Cell Nucleus/virology , Karyopherins/genetics , Karyopherins/metabolism , Nuclear Envelope/metabolism , Nuclear Envelope/virology , Protein Binding , Receptors, Cytoplasmic and Nuclear/genetics , Receptors, Cytoplasmic and Nuclear/metabolism , Rhabdoviridae/metabolism , alpha Karyopherins/genetics
2.
Cancer Chemother Pharmacol ; 74(6): 1241-50, 2014 Dec.
Article in English | MEDLINE | ID: mdl-25304209

ABSTRACT

PURPOSE: ATI-1123 is a liposomal formulation of docetaxel and may be administered without the premedications and hypersensitivity reactions. This Phase I study examines the safety, tolerability, pharmacokinetics (PKs), and antitumor activity of ATI-1123. METHODS: Patients with advanced solid malignancies received escalating doses of ATI-1123 intravenously over 1-h every 3 weeks. The dosing commenced using an accelerated titration design and was followed by a modified 3 + 3 Fibonacci schema to determine maximally tolerated dose (MTD). Plasma was analyzed for encapsulated/non-encapsulated docetaxel; PK analyses were performed using model independent method. Response was assessed using RECIST criteria. RESULTS: In total, 29 patients received doses ranging from 15 to 110 mg/m(2). At 110 mg/m(2), two of six patients experienced dose-limiting toxicities including grade 3 stomatitis and febrile neutropenia. The 90 mg/m(2) cohort was expanded to ten patients and identified as the MTD. The most common adverse events were fatigue, nausea, neutropenia, anemia, anorexia, and diarrhea. ATI-1123 exhibited linear and dose proportional PKs. One patient with lung cancer had confirmed partial response, and stable disease was observed in 75 % patients. CONCLUSIONS: ATI-1123 demonstrated an acceptable tolerability and favorable PK profile in patients with solid tumors. Our results provide support for Phase II trials to determine the antitumor activity of this drug.


Subject(s)
Antineoplastic Agents/administration & dosage , Neoplasms/drug therapy , Taxoids/administration & dosage , Adult , Aged , Aged, 80 and over , Antineoplastic Agents/adverse effects , Antineoplastic Agents/pharmacokinetics , Docetaxel , Dose-Response Relationship, Drug , Female , Humans , Infusions, Intravenous , Liposomes , Male , Maximum Tolerated Dose , Middle Aged , Neoplasms/pathology , Taxoids/adverse effects , Taxoids/pharmacokinetics , Treatment Outcome
3.
J Gen Virol ; 93(Pt 11): 2490-2495, 2012 Nov.
Article in English | MEDLINE | ID: mdl-22837417

ABSTRACT

Impatiens necrotic spot tospovirus (INSV) is a significant pathogen of ornamentals. The tripartite negative- and ambi-sense RNA genome encodes six proteins that are involved in cytoplasmic replication, movement, assembly, insect transmission and defence. To gain insight into the associations of these viral proteins, we determined their intracellular localization and interactions in living plant cells. Nucleotide sequences encoding the nucleoprotein N, non-structural proteins NSs and NSm, and glycoproteins Gn and Gc of a Kentucky isolate of INSV were amplified by RT-PCR, cloned, sequenced and transiently expressed as fusions with autofluorescent proteins in leaf epidermal cells of Nicotiana benthamiana. All proteins accumulated at the cell periphery and co-localized with an endoplasmic reticulum marker. The Gc protein fusion also localized to the nucleus. N and NSm protein self-interactions and an NSm-N interaction were observed by using bimolecular fluorescence complementation. A tospovirus NSm homotypic interaction had not been reported previously.


Subject(s)
Impatiens/virology , Plant Diseases/virology , Tospovirus/classification , Tospovirus/genetics , Cells, Cultured , Gene Expression Regulation, Plant , Gene Expression Regulation, Viral/physiology , Molecular Sequence Data , Plant Epidermis/cytology , Plant Epidermis/virology , Plants, Genetically Modified , Nicotiana/genetics , Nicotiana/virology , Viral Proteins/metabolism
4.
Front Plant Sci ; 3: 14, 2012.
Article in English | MEDLINE | ID: mdl-22645569

ABSTRACT

Potato yellow dwarf virus (PYDV) is the type species of the genus Nucleorhabdovirus and, like all members of this genus, replication and morphogenesis occurs inside the nuclei of infected cells. Protein localization prediction algorithms failed to identify a nuclear localization signal (NLS) in PYDV nucleocapsid (N) protein, although PYDV-N has been shown to localize exclusively to the nucleus when expressed as a green fluorescent protein (GFP):N fusion in plant cells. Deletion analysis using fragments of PYDV-N identified a karyophilic region in the carboxy-terminal 122 amino acids. Alanine-scanning mutagenesis was performed across this region in the context of the full-length N protein. Mutants were assayed for their ability to nuclear localize using live-cell imaging and a yeast-based assay. Two amino acid motifs, (419)QKR(421) and (432)KR(433) were shown to be essential for nuclear import and interaction with importin-α. Additional bimolecular fluorescence complementation showed that the PYDV-N-NLS mutants cannot be ferried into the nucleus via interaction with PYDV-P or -M. In contrast, interaction with N-NLS mutants appeared to retard the nuclear import of PYDV-P. GFP fused to aa 419-434 established that the PYDV-N-NLS can function outside the context of this protein. Taken together, it was determined that PYDV-N contains the bipartite NLS (419)QKRANEEAPPAAQKR(433).

5.
J Med Microbiol ; 60(Pt 10): 1550-1552, 2011 Oct.
Article in English | MEDLINE | ID: mdl-21659503

ABSTRACT

We report a case of a previously healthy 23-year-old Somalian care assistant. She presented with a 4 month history of persistent occipital headaches associated with intermittent nausea and vomiting. Computed tomography and magnetic resonance imaging of the brain showed a large enhancing lesion in the right cerebellar hemisphere with surrounding ring lesions, suggestive of an intracranial neoplasm with metastases. However, tuberculoma of the brain was confirmed based on histology of the excision biopsy and cerebrospinal fluid (CSF) culture results: Mycobacterium tuberculosis resistant to isoniazid (INH) with sensitivity to other standard drugs, including fluoroquinolones, was cultured from CSF. No primary focus to suggest spread from elsewhere was found. The patient was treated successfully with moxifloxacin, rifampicin, pyrazinamide and ethambutol. Isolated INH-resistant intracranial tuberculoma is rare in adults. It can mimic other intracranial masses and should be kept in mind, especially in populations with a high risk of tuberculosis. Clinical use of moxifloxacin in INH-resistant tuberculomas is limited in humans and this case demonstrates that moxifloxacin may be an effective alternative treatment.


Subject(s)
Antitubercular Agents/administration & dosage , Aza Compounds/administration & dosage , Drug Resistance, Bacterial , Quinolines/administration & dosage , Tuberculoma, Intracranial/diagnosis , Tuberculoma, Intracranial/drug therapy , Tuberculosis, Multidrug-Resistant/diagnosis , Tuberculosis, Multidrug-Resistant/drug therapy , Antitubercular Agents/pharmacology , Biopsy , Brain/diagnostic imaging , Brain/microbiology , Brain/pathology , Cerebrospinal Fluid/microbiology , Ethambutol/administration & dosage , Female , Fluoroquinolones , Histocytochemistry , Humans , Isoniazid/pharmacology , Magnetic Resonance Imaging , Moxifloxacin , Mycobacterium tuberculosis/drug effects , Mycobacterium tuberculosis/isolation & purification , Pyrazinamide/administration & dosage , Rifampin/administration & dosage , Tomography, X-Ray Computed , Treatment Outcome , Tuberculoma, Intracranial/microbiology , Tuberculosis, Multidrug-Resistant/microbiology , Young Adult
6.
Virology ; 402(1): 61-71, 2010 Jun 20.
Article in English | MEDLINE | ID: mdl-20362316

ABSTRACT

The genome of Potato yellow dwarf virus (PYDV; Nucleorhabdovirus type species) was determined to be 12,875 nucleotides (nt). The antigenome is organized into seven open reading frames (ORFs) ordered 3'-N-X-P-Y-M-G-L-5', which likely encode the nucleocapsid, phospho, movement, matrix, glyco and RNA-dependent RNA polymerase proteins, respectively, except for X, which is of unknown function. The ORFs are flanked by a 3' leader RNA of 149 nt and a 5' trailer RNA of 97 nt, and are separated by conserved intergenic junctions. Phylogenetic analyses indicated that PYDV is closely related to other leafhopper-transmitted rhabdoviruses. Functional protein assays were used to determine the subcellular localization of PYDV proteins. Surprisingly, the M protein was able to induce the intranuclear accumulation of the inner nuclear membrane in the absence of any other viral protein. Finally, bimolecular fluorescence complementation was used to generate the most comprehensive protein interaction map for a plant-adapted rhabdovirus to date.


Subject(s)
Protein Interaction Mapping , Rhabdoviridae/physiology , Solanum tuberosum/virology , Viral Proteins/metabolism , 3' Untranslated Regions , 5' Untranslated Regions , Cell Nucleus/chemistry , Cluster Analysis , Cytoplasm/chemistry , DNA, Intergenic , Gene Order , Genome, Viral , Microscopy, Confocal , Molecular Sequence Data , Nuclear Envelope/chemistry , Open Reading Frames , Phylogeny , Protein Binding , RNA, Viral/genetics , Rhabdoviridae/genetics , Rhabdoviridae/metabolism , Sequence Analysis, DNA , Sequence Homology , Nicotiana/virology , Two-Hybrid System Techniques , Viral Proteins/genetics
7.
Chest ; 132(3): 1044-8, 2007 Sep.
Article in English | MEDLINE | ID: mdl-17873199

ABSTRACT

BACKGROUND: Though more common in male patients, primary spontaneous pneumothorax might be expected to occur reasonably often in female patients of child-bearing age. However, < 50 cases of pneumothorax in pregnancy have been previously reported. Special risks are posed for both the mother and the fetus in this situation. Previous management strategies have varied widely, without describing the more modern and less invasive techniques, and existing pneumothorax guidelines do not incorporate this difficult scenario. METHODS: A retrospective search of our database of 250 spontaneous pneumothorax patients over a 10-year period, in a stable local population of 500,000 patients, identified five cases of pneumothorax occurring in pregnancy. We report our experience, the largest series yet described, review the medical literature, and make management recommendations. RESULTS: We found favorable outcomes for both mothers and infants in our series, with modern techniques such as simple aspiration, elective assisted delivery at or near term with regional anesthesia, and video-assisted thoracoscopic surgery. CONCLUSIONS: Future guidelines on the management of pneumothorax should consider the inclusion of advice on the problems of pregnancy, based on previous published experience, and utilizing the modern and less invasive techniques. Such advice would inform and support those specialists involved in managing a potentially hazardous situation to the benefit of both mother and child.


Subject(s)
Pneumothorax/diagnosis , Pneumothorax/therapy , Pregnancy Complications/diagnosis , Pregnancy Complications/therapy , Adult , Female , Humans , Pregnancy , Pregnancy Outcome
8.
Nat Genet ; 34(2): 181-6, 2003 Jun.
Article in English | MEDLINE | ID: mdl-12754510

ABSTRACT

Atopic or immunoglobulin E (IgE)-mediated diseases include the common disorders of asthma, atopic dermatitis and allergic rhinitis. Chromosome 13q14 shows consistent linkage to atopy and the total serum IgE concentration. We previously identified association between total serum IgE levels and a novel 13q14 microsatellite (USAT24G1; ref. 7) and have now localized the underlying quantitative-trait locus (QTL) in a comprehensive single-nucleotide polymorphism (SNP) map. We found replicated association to IgE levels that was attributed to several alleles in a single gene, PHF11. We also found association with these variants to severe clinical asthma. The gene product (PHF11) contains two PHD zinc fingers and probably regulates transcription. Distinctive splice variants were expressed in immune tissues and cells.


Subject(s)
Asthma/genetics , Chromosomes, Human, Pair 13/genetics , Immunoglobulin E/blood , Quantitative Trait Loci , Adult , Alleles , Alternative Splicing , Case-Control Studies , Child , Female , Haplotypes , Humans , Male , Molecular Sequence Data , Polymorphism, Single Nucleotide , Tissue Distribution , Zinc Fingers/genetics
9.
Eur J Hum Genet ; 10(4): 266-70, 2002 Apr.
Article in English | MEDLINE | ID: mdl-12032735

ABSTRACT

Linkage of atopy and associated traits to a locus on chromosome 13q14 has been identified by several studies in diverse populations. We have previously shown the putative atopy gene to be contained within an interval of approximately 5 Mb flanked by D13S328 and D13S1269 and centred on D13S273. We have now extended this work using a top-down approach to physical mapping. A YAC contig was constructed covering the D13S328 and D13S1269 interval. Thirty-one ESTs were mapped to the contig. We constructed a BAC and PAC contig flanking D13S273 by approximately 750 kb in either direction. The interval contained 27 of the 31 ESTS from the YAC contig. Seven previously unknown microsatellites were recovered and then typed in two subject panels. A positive association between the total serum Immunoglobulin E concentration and the novel USAT24G1 microsatellite was discovered (P(corrected)<0.005) and replicated in a second panel of families. The discovery of a region of positive association within the BAC/PAC contig will permit identification of the atopy gene from this locus.


Subject(s)
Chromosomes, Human, Pair 13/genetics , Genetic Linkage , Hypersensitivity, Immediate/genetics , Immunoglobulin E/blood , Adolescent , Adult , Child , Female , Humans , Male , Microsatellite Repeats/genetics , Physical Chromosome Mapping/methods
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