Host age increased conjugal plasmid transfer in gut microbiota of the soil invertebrate Caenorhabditis elegans

2021 ◽  
pp. 127525
Author(s):  
Guo-Wei Zhou ◽  
Fei Zheng ◽  
Xiao-Ting Fan ◽  
Ming-Jun Li ◽  
Qing-Ye Sun ◽  
...  
2016 ◽  
Vol 10 (8) ◽  
pp. 1998-2009 ◽  
Author(s):  
Maureen Berg ◽  
Ben Stenuit ◽  
Joshua Ho ◽  
Andrew Wang ◽  
Caitlin Parke ◽  
...  

2020 ◽  
Vol 260 ◽  
pp. 113991
Author(s):  
Guo-Wei Zhou ◽  
Xiao-Ru Yang ◽  
Fei Zheng ◽  
Zi-Xing Zhang ◽  
Bang-Xiao Zheng ◽  
...  

2021 ◽  
Author(s):  
Jun Zheng ◽  
Xin Meng ◽  
Jiahao Fan ◽  
Dong Yang

AbstractThe past forty-five years has witnessed Caenorhabditis elegans as the most significant model animal in life science since its discovery seventy years ago1,2, as it introduced principles of gene regulated organ development, and RNA interference into biology3-5. Meanwhile, it has become one of the lab animals in gut microbiota studies as these symbionts contribute significantly to many aspects in host biology6,7. Meanwhile, the origin of gut microbiota remains debatable in human8- 11, and has not been investigated in other model animals. Here we show that the symbiont bacteria in C. elegans not only vertically transmit from the parent generation to the next, but also distributes in the worm tissues parallel with its development. We found that bacteria can enter into the embryos of C. elegans, a step associated with vitellogenin, and passed to the next generation. These vertically transmitted bacteria share global similarity, and bacterial distribution in worm tissues changes as they grow at different life stages. Antibiotic treatment of worms increased their vulnerability against pathogenic bacteria, and replenishment of tissue microbiota restored their immunity. These results not only offered a molecular basis of vertical transmission of bacteria in C. elegans, but also signal a new era for the mixed tissue cell-bacteria multi-species organism study.


2016 ◽  
Vol 78 (8) ◽  
pp. 883-892 ◽  
Author(s):  
Genevieve Bennett ◽  
Matthew Malone ◽  
Michelle L. Sauther ◽  
Frank P. Cuozzo ◽  
Bryan White ◽  
...  

2002 ◽  
Vol 69 ◽  
pp. 117-134 ◽  
Author(s):  
Stuart M. Haslam ◽  
David Gems ◽  
Howard R. Morris ◽  
Anne Dell

There is no doubt that the immense amount of information that is being generated by the initial sequencing and secondary interrogation of various genomes will change the face of glycobiological research. However, a major area of concern is that detailed structural knowledge of the ultimate products of genes that are identified as being involved in glycoconjugate biosynthesis is still limited. This is illustrated clearly by the nematode worm Caenorhabditis elegans, which was the first multicellular organism to have its entire genome sequenced. To date, only limited structural data on the glycosylated molecules of this organism have been reported. Our laboratory is addressing this problem by performing detailed MS structural characterization of the N-linked glycans of C. elegans; high-mannose structures dominate, with only minor amounts of complex-type structures. Novel, highly fucosylated truncated structures are also present which are difucosylated on the proximal N-acetylglucosamine of the chitobiose core as well as containing unusual Fucα1–2Gal1–2Man as peripheral structures. The implications of these results in terms of the identification of ligands for genomically predicted lectins and potential glycosyltransferases are discussed in this chapter. Current knowledge on the glycomes of other model organisms such as Dictyostelium discoideum, Saccharomyces cerevisiae and Drosophila melanogaster is also discussed briefly.


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