scholarly journals Genomic molecular signatures determined characterization of Mycolicibacterium gossypii sp. nov., a fast-growing mycobacterial species isolated from cotton field soil

Author(s):  
Rui-Rui Huang ◽  
Shen-Rong Yang ◽  
Cheng Zhen ◽  
Xian-Feng Ge ◽  
Xin-Kai Chen ◽  
...  
2021 ◽  
Author(s):  
Ruirui Huang ◽  
Shenrong Yang ◽  
Cheng Zhen ◽  
Xianfeng Ge ◽  
Xinkai Chen ◽  
...  

Abstract A Gram-positive, acid-fast and rapidly growing rod, designated S2-37 T , that could form yellowish colonies was isolated from soil samples collected from cotton cropping field located in the Xinjiang region of China. The draft genome of strain S2-37 T was 5.1 Mb in length, with a DNA G+C content of 68.4 mol%. 16S rRNA-directed phylogenetic analysis referred that strain S2-37 T was closely related to bacterial species belonging to the genus Mycolicibacterium and Mycobacterium . Multilocus sequence analysis of three genes (16S rRNA, hsp65 and rpoB ) revealed that strain S2-37 T shared high sequence similarities with Mycolicibacterium litorale CGMCC 4.5724 T (96.5%) and Mycobacterium neglectum CECT 8778 T (95.7%). Digital DNA-DNA hybridization (dDDH) and the average nucleotide identity (ANI) presented that strainS2-37 T displayed the highest values of 39.1% (35.7-42.6%) and 81.28% with M. litorale CGMCC 4.5724 T , respectively. And characterazition of conserved molecular signatures further confirmed that strain S2-37 T could be well classified into the genus Mycolicibacterium . The main fatty acids were identified as C 16:0 , C 18:0 , C 20:3 ω3 and C 22:6 ω3 . In addition, polar lipids profile was mainly composed of diphosphatidylglycerol, phosphatidylethanolamine and phosphatidylinositol. Results indicated that strain S2-37 T represented genetically and phenotypically distinct from its closest phylogenetic neighbour, M. litorale CGMCC 4.5724 T . Here, we propose a novel species of the genus Mycolicibacterium : Mycolicibacterium gossypii sp. nov. with the type strain S2-37 T (=JCM 34327T =CGMCC 1.18817T ).


2020 ◽  
Author(s):  
Margarita Smirnova ◽  
Uladzislau Miamin ◽  
Achim Kohler ◽  
Leonid Valentovich ◽  
Artur Akhremchuk ◽  
...  

2012 ◽  
Vol 2012 ◽  
pp. 1-9 ◽  
Author(s):  
Zhiqiang Qin ◽  
Andrew Jakymiw ◽  
Victoria Findlay ◽  
Chris Parsons

The human genome contains microRNAs (miRNAs), small noncoding RNAs that orchestrate a number of physiologic processes through regulation of gene expression. Burgeoning evidence suggests that dysregulation of miRNAs may promote disease progression and cancer pathogenesis. Virus-encoded miRNAs, exhibiting unique molecular signatures and functions, have been increasingly recognized as contributors to viral cancer pathogenesis. A large segment of the existing knowledge in this area has been generated through characterization of miRNAs encoded by the human gamma-herpesviruses, including the Kaposi’s sarcoma-associated herpesvirus (KSHV). Recent studies focusing on KSHV miRNAs have led to a better understanding of viral miRNA expression in human tumors, the identification of novel pathologic check points regulated by viral miRNAs, and new insights for viral miRNA interactions with cellular (“human”) miRNAs. Elucidating the functional effects of inhibiting KSHV miRNAs has also provided a foundation for further translational efforts and consideration of clinical applications. This paper summarizes recent literature outlining mechanisms for KSHV miRNA regulation of cellular function and cancer-associated pathogenesis, as well as implications for interactions between KSHV and human miRNAs that may facilitate cancer progression. Finally, insights are offered for the clinical feasibility of targeting miRNAs as a therapeutic approach for viral cancers.


Author(s):  
Marco A. Riojas ◽  
Andrew M. Frank ◽  
Samuel R. Greenfield ◽  
Stephen P. King ◽  
Conor J. Meehan ◽  
...  

2014 ◽  
Author(s):  
Jamie N. Hadac ◽  
Terrah J. Paul Olson ◽  
Alyssa A. Leystra ◽  
Dawn M. Albrecht ◽  
Linda Clipson ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document