27 research outputs found
Genome Sequence of \u3ci\u3eStreptomyces aureofaciens\u3c/i\u3e ATCC Strain 10762
Streptomyces aureofaciens is a Gram-positive actinomycete that produces the antibiotics tetracycline and chlortetracycline. Here, we report the assembly and initial annotation of the draft genome sequence of S. aureofaciens ATCC strain 10762
Genome Sequence of \u3ci\u3eStreptomyces aureofaciens\u3c/i\u3e ATCC Strain 10762
Streptomyces aureofaciens is a Gram-positive actinomycete that produces the antibiotics tetracycline and chlortetracycline. Here, we report the assembly and initial annotation of the draft genome sequence of S. aureofaciens ATCC strain 10762
An attenuated herpesvirus vectored vaccine candidate induces T-cell responses against highly conserved porcine reproductive and respiratory syndrome virus M and NSP5 proteins that are unable to control infection
Porcine reproductive and respiratory syndrome virus (PRRSV) remains a leading cause of economic loss in pig farming worldwide. Existing commercial vaccines, all based on modified live or inactivated PRRSV, fail to provide effective immunity against the highly diverse circulating strains of both PRRSV-1 and PRRSV-2. Therefore, there is an urgent need to develop more effective and broadly active PRRSV vaccines. In the absence of neutralizing antibodies, T cells are thought to play a central role in controlling PRRSV infection. Herpesvirus-based vectors are novel vaccine platforms capable of inducing high levels of T cells against encoded heterologous antigens. Therefore, the aim of this study was to assess the immunogenicity and efficacy of an attenuated herpesvirus-based vector (bovine herpesvirus-4; BoHV-4) expressing a fusion protein comprising two well-characterized PRRSV-1 T-cell antigens (M and NSP5). Prime-boost immunization of pigs with BoHV-4 expressing the M and NSP5 fusion protein (vector designated BoHV-4-M-NSP5) induced strong IFN-γ responses, as assessed by ELISpot assays of peripheral blood mononuclear cells (PBMC) stimulated with a pool of peptides representing PRRSV-1 M and NSP5. The responses were closely mirrored by spontaneous IFN-γ release from unstimulated cells, albeit at lower levels. A lower frequency of M and NSP5 specific IFN-γ responding cells was induced following a single dose of BoHV-4-M-NSP5 vector. Restimulation using M and NSP5 peptides from PRRSV-2 demonstrated a high level of cross-reactivity. Vaccination with BoHV-4-M-NSP5 did not affect viral loads in either the blood or lungs following challenge with the two heterologous PRRSV-1 strains. However, the BoHV-4-M-NSP5 prime-boost vaccination showed a marked trend toward reduced lung pathology following PRRSV-1 challenge. The limited effect of T cells on PRRSV-1 viral load was further examined by analyzing local and circulating T-cell responses using intracellular cytokine staining and proliferation assays. The results from this study suggest that vaccine-primed T-cell responses may have helped in the control of PRRSV-1 associated tissue damage, but had a minimal, if any, effect on controlling PRRSV-1 viral loads. Together, these results indicate that future efforts to develop effective PRRSV vaccines should focus on achieving a balanced T-cell and antibody response
A novel approach in the treatment of neuroendocrine gastrointestinal tumors: Additive antiproliferative effects of interferon-γ and meta-iodobenzylguanidine
BACKGROUND: Therapeutic options to effectively inhibit growth and spread of neuroendocrine gastrointestinal tumors are still limited. As both meta-iodobenzylguanidine (MIBG) and interferon-γ (IFNγ) cause antineoplastic effects in neuroendocrine gastrointestinal tumor cells, we investigated the antiproliferative effects of the combination of IFNγ and non-radiolabeled MIBG in neuroendocrine gut STC-1 and pancreatic carcinoid BON tumor cells. METHODS AND RESULTS: IFNγ receptors were expressed in both models. IFNγ dose- and time-dependently inhibited the growth of both STC-1 and of BON tumor cells with IC(50)-values of 95 ± 15 U/ml and 135 ± 10 U/ml, respectively. Above 10 U/ml IFNγ induced apoptosis-specific caspase-3 activity in a time-dependent manner in either cell line and caused a dose-dependent arrest in the S-phase of the cell cycle. Furthermore, IFNγ induced cytotoxic effects in NE tumor cells. The NE tumor-targeted drug MIBG is selectively taken up via norepinephrine transporters, thereby specifically inhibiting growth in NE tumor cells. Intriguingly, IFNγ treatment induced an upregulation of norepinephrine transporter expression in neuroendocrine tumors cells, as determined by semi-quantitative RT-PCR. Co-application of sub-IC(50 )concentrations of IFNγ and MIBG led to additive growth inhibitory effects, which were mainly due to increased cytotoxicity and S-phase arrest of the cell cycle. CONCLUSION: Our data show that IFNγ exerts antiproliferative effects on neuroendocrine gastrointestinal tumor cells by inducing cell cycle arrest, apoptosis and cytotoxicity. The combination of IFNγ with the NE tumor-targeted agent MIBG leads to effective growth control at reduced doses of either drug. Thus, the administration of IFNγ alone and more so, in combination with MIBG, is a promising novel approach in the treatment of neuroendocrine gastrointestinal tumors
Fig. 1 in Use of Morphology and CO1 Barcoding to Test the Validity ofTetraopes huetheriSkillman (Coleoptera: Cerambycidae)
Fig. 1. Protarsus of Tetraopes huetheri, paratype.Published as part of <i>Etzler, Frank E., Huether, Jeffery, Johnson, Paul J., Skillman, Frederick W. & Ivie, Michael A., 2013, Use of Morphology and CO1 Barcoding to Test the Validity ofTetraopes huetheriSkillman (Coleoptera: Cerambycidae), pp. 45-49 in The Coleopterists Bulletin 67 (1)</i> on page 47, DOI: 10.1649/072.067.0110, <a href="http://zenodo.org/record/10110560">http://zenodo.org/record/10110560</a>
Use of Morphology and CO1 Barcoding to Test the Validity ofTetraopes huetheriSkillman (Coleoptera: Cerambycidae)
Etzler, Frank E., Huether, Jeffery, Johnson, Paul J., Skillman, Frederick W., Ivie, Michael A. (2013): Use of Morphology and CO1 Barcoding to Test the Validity ofTetraopes huetheriSkillman (Coleoptera: Cerambycidae). The Coleopterists Bulletin 67 (1): 45-49, DOI: 10.1649/072.067.0110, URL: http://dx.doi.org/10.1649/072.067.011
Fig. 2 in Use of Morphology and CO1 Barcoding to Test the Validity ofTetraopes huetheriSkillman (Coleoptera: Cerambycidae)
Fig. 2. Neighbor-Joining tree of 22 Tetraopes specimens and data from Farrell (2001). Scale indicates 1% difference.Published as part of <i>Etzler, Frank E., Huether, Jeffery, Johnson, Paul J., Skillman, Frederick W. & Ivie, Michael A., 2013, Use of Morphology and CO1 Barcoding to Test the Validity ofTetraopes huetheriSkillman (Coleoptera: Cerambycidae), pp. 45-49 in The Coleopterists Bulletin 67 (1)</i> on page 48, DOI: 10.1649/072.067.0110, <a href="http://zenodo.org/record/10110560">http://zenodo.org/record/10110560</a>