Rainbow trout farming is a major food source industry worldwide that has suffered great economic losses due to host jumps of fish rhabdovirus pathogens, followed by evolution of dramatic increases in trout-specific virulence. However, the genetic determinants of host jumps and increased virulence in rainbow trout are unknown for any fish rhabdovirus. Previous attempts to identify the viral genes containing trout virulence determinants of viral hemorrhagic septicemia virus (VHSV) have not been successful. We show here that, somewhat surprisingly, the viral nucleocapsid (N) and phosphoprotein (P) genes together contain the determinants responsible for trout virulence in VHSV. This suggests a novel host-specific virulence mechanism involving the viral polymerase and a host component. This differs from the known virulence mechanisms of mammalian rhabdoviruses based on the viral P or M (matrix) protein.
Complement-containing immune complexes can be presented to phagocytes by human erythrocytes bearing complement receptor 1 (CR1). Although this has long been assumed to be a mechanism by which humans are able to protect themselves from "extracellular" bacteria such as pneumococci, there is little direct evidence. In these studies we have investigated this question by comparing results for erythrocytes from transgenic mice expressing human CR1 on their erythrocytes to the results for wild-type mouse erythrocytes that do not express CR1. We demonstrate that human CR1 expression on murine erythrocytes allows immune adherence to beads opsonized with either mouse or human serum as a source of complement. The role of CR1 in immune adherence was supported by studies showing that it was blocked by the addition of antibody to human CR1. Furthermore, human CR1 expression enhances the immune adherence of opsonized pneumococci to erythrocytes in vitro, and the pneumococci attached to erythrocytes via CR1 can be transferred in vitro to live macrophages. Even more importantly, we observed that if complement-opsonized pneumococci are injected intravenously with CR1(+) mouse erythrocytes into wild-type mice (after a short in vitro incubation), they are cleared faster than opsonized pneumococci similarly injected with wild-type mouse erythrocytes. Finally, we have shown that the intravenous (i.v.) injection of pneumococci into CR1(+) mice also results in more rapid blood clearance than in wild-type mice. These data support that immune adherence via CR1 on erythrocytes likely plays an important role in the clearance of opsonized bacteria from human blood.
Turbot ( Scophthalmus maximus ) is an important commercial fish in China that can be infected by a series of bacterial pathogens, leading to great economic losses. In this study we focused on the epidemiology of turbot bacterial diseases in the major farming areas in China for three years. A total of 155 cases with 446 diseased turbots were investigated, and dominant bacterial pathogens were isolated from 137 cases (344 turbots). Thus, bacteria are the major threat to farming turbot in China. Edwardsiella piscicida was the major pathogen, which isolated as the dominant colony in 62 cases (40.00%) with 151 turbots (33.85%). Aeromonas salmonicida was isolated in 57 cases (36.77%) with 116 turbots (26.01%). Vibrio anguillarum was isolated in nine cases (5.81%), and Streptococcus parauberis in five cases (3.23%). Photobacterium damselae and Mycobacterium marinum were also isolated from one or two diseased fish. Other Vibrio spp. were isolated in 15 cases (9.68%). Two species of pathogen were isolated in 13 cases, and three species ( E. piscicida , A . salmonicida , and S . parauberis ) in one case. In 19 cases, no bacteria were isolated. Based on the annual disease analysis, we found that the E . piscicida infection proportion of total cases was greatly decreased, which may be caused by the attenuated vaccine inoculated in 2018. The antibiotic resistance of E . piscicida strains isolated in Weifang city was also determined. We found that the resistance to ceftriaxone, doxycycline, and SMZ/TMP were significantly increased from October 2016 to June 2018, and all the E . piscicida isolates exhibited resistance to SMZ/TMP in June 2018. These results indicated that E . piscicida is the major threat to turbot farming in China, and the attenuated E . piscicida vaccine exhibits effective protection. The usage of antibiotics may induce resistance quickly. Thus, development of vaccines is an important work for sustainable development of turbot farming in the future.
TTC39A (tetratricopeptide repeat domain protein 39A) belongs to the structural family of tetratrico-peptide domain proteins. TTC39A had not been researched in cancers. The purpose of this study was to reveal the potential role of TTC39A in cancers. In total, 33 cancers were included in this study. All the data came from the Cancer Genome Atlas (TCGA) database. The expression of TTC39A was explored in the 33 cancers. The relationship between the expression of TTC39A and prognosis, clinical characteristics, and immune infiltration was also explored. Paraffin-embedded cancer tissue microarrays (TMA) were used to detect the expression of TTC39A in LIHC (liver hepatocellular carcinoma) and LGG (brain lower grade glioma). The expression of TTC39A was higher in many cancers, compared with the corresponding normal tissues. For patients with LGG, LIHC, and SKCM (skin cutaneous melanoma), higher expression of TTC39A indicated worse OS. Survival analysis in clinical samples indicated that high expression of TTC39A was associated with shorter overall survival. The expression of TTC39A was related to the immune infiltration of some immune cells in LGG, LIHC, and SKCM. Also, the expression of TTC39A combined with the immune infiltration level of some immune cells could affect the OS of patients with these three cancers. Functional enrichment analysis and gene set enrichment analysis (GSEA) showed that TTC39A might play a role in many biological processes. The expression of TTC39A was significantly higher in many cancers. TTC39A was associated with the prognosis of patients with LGG, LIHC, and SKCM, whether they were combined with the immune infiltration level of some immune cells or not. In these three cancers, TTC39A might play a role in some important biological processes.
Sterile α motif and histidine/aspartic acid domain‑containing protein 1 (SAMHD1) can inhibit reverse transcription of human immunodeficiency virus‑1 (HIV‑1) by hydrolyzing intracellular deoxy‑ribonucleoside triphosphate. However, its role in HIV‑1 disease progression has not been extensively studied. To study the impacts of SAMHD1 on HIV‑1 disease progression, especially on DNA levels, we investigated SAMHD1 levels in the peripheral blood of HIV‑1 elite controllers (ECs), antiretroviral therapy (ART) naive viremic progressors (VPs) and patients with HIV‑1 receiving ART (HIV‑ARTs) compared with healthy controls. In addition, the present study analyzed the relationship between SAMHD1 and interferon‑α, immune activation and HIV‑1 DNA levels. The results of the present study demonstrated elevated SAMHD1 expression in the peripheral blood mononuclear cells of all patients withHIV‑1, but higher SAMHD1 expression in the CD4+ T cells of only ECs compared with healthy controls. Immune activation was increased in the VPs and decreased in the ECs compared with healthy controls. Substantially lower HIV‑1 DNA levels were identified in ECs compared with those in VPs and HIV‑ARTs. SAMHD1 expression was associated with low levels of immune activation. No significant correlation was observed between SAMHD1 and HIV‑1 DNA levels. Overall, the findings of the present study indicated that SAMHD1 was highly expressed in ECs, which may be associated with low immune activation levels, but was not directly related to HIV‑1 DNA levels.
Trichosanthin is the active protein component in the Chinese herb Trichosanthes kirilowi, which has distinct pharmacological properties. The cytotoxicity of trichosanthin was demonstrated by its selective inhibition of various choriocarcinoma cells. When Jar cells were treated with trichosanthin, the influx of calcium into the cells was observed by confocal laser scanning microscopy. When the distribution of trichosanthin-binding proteins on Jar cells was studied, two classes of binding sites for trichosanthin were shown by radioligand binding assay. Furthermore, the cytoplasmic membrane of Jar cells was biotinylated and the trichosanthin-binding proteins were isolated with trichosanthin-coupled Sepharose beads. Two protein bands with molecular masses of about 50 kDa and 60 kDa were revealed, further characterization of which should shed light on the mechanism of the selective cytotoxicity of trichosanthin to Jar cells.
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