Human adenoviruses (HAdVs) can infect various epithelial mucosal cells, ultimately causing different symptoms in infected organ systems. With more than 110 types classified into seven species (A-G), HAdV-D species possess the highest number of viruses and are the fastest proliferating. The emergence of new adenovirus types and increased diversity are driven by homologous recombination (HR) between viral genes, primarily in structural elements such as the penton base, hexon and fiber proteins, and the E1 and E3 regions. A comprehensive analysis of the HAdV genome provides valuable insights into the evolution of human adenoviruses and identifies genes that display high variation across the entire genome to determine recombination patterns. Hypervariable regions within genetic sequences correlate with functional characteristics, thus allowing for adaptation to new environments and hosts. Proteotyping of newly emerging and already established adenoviruses allows for prediction of the characteristics of novel viruses. HAdV-D species evolved in a direction that increased diversity through gene recombination. Bioinformatics analysis across the genome, particularly in highly variable regions, allows for the verification or re-evaluation of recombination patterns in both newly introduced and pre-existing viruses, ultimately aiding in tracing various biological traits such as virus tropism and pathogenesis. Our research does not only assist in predicting the emergence of new adenoviruses but also offers critical guidance in regard to identifying potential regulatory factors of homologous recombination hotspots.
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In Silico Intensive Analysis for the E4 Gene Evolution of Human Adenovirus Species D Chanhee Lee, Anyeseu Park, Jeong Yoon Lee Journal of Microbiology.2024; 62(5): 409. CrossRef
Due to the ever-increasing demand for meat, it has become necessary to identify cheap and sustainable sources of protein for animal feed. Feathers are the major byproduct of poultry industry, which are rich in hard-to-degrade keratin protein.
Previously we found that intact feathers can be digested into free amino acids, short peptides, and nano-/micro-keratin particles by the strain Bacillus licheniformis WHU in water, and the resulting feather hydrolysates exhibit prebiotic effects on mice. To explore the potential utilization of feather hydrolysate in the feed industry, we investigated its effects on the gut microbiota of broilers and fish. Our results suggest that feather hydrolysates significantly decrease and increase the diversity of gut microbial communities in broilers and fish, respectively. The composition of the gut microbiota was markedly altered in both of the animals. The abundance of bacteria with potentially pathogenic phenotypes in the gut microbial community of the fish significantly decreased. Staphylococcus spp., Pseudomonas spp., Neisseria spp., Achromobacter spp. were significantly inhibited by the feather hydrolysates. In addition, feather hydrolysates significantly improved proteolytic activity in the guts of broilers and fish. In fish, the expression levels of ZO-1 and TGF-α significantly improved after administration of feather hydrolysates. The results presented here suggest that feather hydrolysates generated by B. licheniformis WHU could be an alternative protein source in aquaculture and could exert beneficial effects on fish.
Stenotrophomonas maltophilia (S. maltophilia) is a common
opportunistic pathogen in intensive care units and causes infections
most often after surgeries in immune-compromised
patients such as those undergoing chemotherapy. Outer membrane
protein A (OmpA) is the most abundant of the outer
membrane proteins in S. maltophilia. Previous studies on
OmpA usually focus on its interaction with the host cells and
its role in vaccine development. However, the impact of
OmpA on the virulence of S. maltophilia to host cells and
the effects on apoptosis remain unclear. In this study, we exposed
purified recombinant S. maltophilia OmpA (rOmpA)
to HEp-2 cells and investigated the effects of OmpA on epithelial
cell apoptosis. Morphologic and flow cytometric analyses
revealed that HEp-2 cells stimulated with rOmpA multiple
apoptosis features, including nuclear roundness and pyknosis,
chromatin aggregation, and phosphatidylserine eversion.
We found that rOmpA regulated the protein levels of
Bax and Bcl-xL in HEp-2 cells, leading to changes in mitochondria
permeability and the release of cytochrome c and
apoptosis-inducing factors into the cytoplasm. These subsequently
activate the caspase-9/caspase-3 pathway that promote
apoptosis. We also observed that rOmpA enhanced the
generation of reactive oxygen species and increased intracellular
Ca2+ levels in HEp-2 cells. Collectively, our data suggested
that rOmpA induced epithelial cells apoptosis via mitochondrial
pathways.
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Functional analysis of OmpA and its contribution to pathogenesis of Edwardsiella tarda Quan Zhou, Yushuai Hu, Yicheng You, Yingli Gao, Xingqiang Wang, Lei Qin Microbial Pathogenesis.2024; 193: 106760. CrossRef
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Bmi-1RNAi
-PTX nanoparticles in suppression of laryngeal cancer by targeting cancer stem cells
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Control of host mitochondria by bacterial pathogens Saverio Marchi, Gianluca Morroni, Paolo Pinton, Lorenzo Galluzzi Trends in Microbiology.2022; 30(5): 452. CrossRef
Lysophosphatidic acid protects cervical cancer HeLa cells from apoptosis induced by doxorubicin hydrochloride Xibo Wang, Haihua Wang, Xiaoxiao Mou, Yilin Xu, Wenbo Han, Aimin Huang, Yanwei Li, Hui Jiang, Xiaoyun Yang, Zhenbo Hu Oncology Letters.2022;[Epub] CrossRef