scholarly journals Recurrent DNA virus domestication leading to different parasite virulence strategies

2015 ◽  
Vol 1 (10) ◽  
pp. e1501150 ◽  
Author(s):  
Apolline Pichon ◽  
Annie Bézier ◽  
Serge Urbach ◽  
Jean-Marc Aury ◽  
Véronique Jouan ◽  
...  

Relics of ancient infections are abundant in eukaryote genomes, but little is known about how they evolve when they confer a functional benefit on their host. We show here, for the first time, that the virus-like particles shown to protect Venturia canescens eggs against host immunity are derived from a nudivirus genome incorporated by the parasitic wasp into its own genetic material. Nudivirus hijacking was also at the origin of protective particles from braconid wasps. However, we show here that the viral genes produce “liposomes” that wrap and deliver V. canescens virulence proteins, whereas the particles are used as gene transfer agents in braconid wasps. Our findings indicate that virus domestication has occurred repeatedly during parasitic wasp evolution but with different evolutionary trajectories after endogenization, resulting in different virulence molecule delivery strategies.

Author(s):  
N. G. Rudova ◽  
V. I. Bolotin ◽  
O. S. Solodiankin ◽  
А. P. Gerilovych

Porcine circovirus type 2 (PCV2) is an emergent single-stranded DNA virus found all over the world in domestic pigs and wild boars that causes infectious disease with a great impact on swine productivity. PCV2 has 1.7 kb genome that includes two main genes, which encode replication-related protein (rep) and the major structural capsid (cap) protein. Both of these genes can be used as target sequences for the primer design for the detection of PCV2 as well as for sequencing of designated regions. We carried out a screening due to the PCV2 circulating among the wild boar population in 10 regions of Ukraine. PCR screening was performed using primer pairs designed on the target sequences of the replicative and capsid genes. According to the results of the research, the presence of genetic material of PCV2 was found in 31.8% of the tested samples. The developed set of primers may be suitable for diagnostics, as well as for the development of specific sites for the purpose of sequencing of PCV2 cap-gene due to the obtained DNA samples during epizootic screening


Pharmaceutics ◽  
2020 ◽  
Vol 12 (8) ◽  
pp. 768
Author(s):  
Noam Y. Steinman ◽  
Luis M. Campos ◽  
Yakai Feng ◽  
Abraham J. Domb ◽  
Hossein Hosseinkhani

Non-viral vectors for the transfection of genetic material are at the frontier of medical science. In this article, we introduce for the first time, cyclopropenium-containing nanoparticles as a cationic carrier for gene transfection, as an alternative to the common quaternary ammonium transfection agents. Cyclopropenium-based cationic nanoparticles were prepared by crosslinking poly(ethylene imine) (PEI) with tetrachlorocyclopropene. These nanoparticles were electrostatically complexed with plasmid DNA into nanoparticles (~50 nm). Their cellular uptake into F929 mouse fibroblast cells, and their eventual expression in vitro have been described. Transfection is enhanced relative to PEI with minimal toxicity. These cyclopropenium nanoparticles possess efficient gene transfection capabilities with minimal cytotoxicity, which makes them novel and promising candidates for gene therapy.


2019 ◽  
Vol 2019 ◽  
pp. 1-11 ◽  
Author(s):  
María V. Villagrana-Escareño ◽  
Elizabeth Reynaga-Hernández ◽  
Othir G. Galicia-Cruz ◽  
Ana L. Durán-Meza ◽  
Viridiana De la Cruz-González ◽  
...  

Virus-like particles (VLPs) are being used for therapeutic developments such as vaccines and drug nanocarriers. Among these, plant virus capsids are gaining interest for the formation of VLPs because they can be safely handled and are noncytotoxic. A paradigm in virology, however, is that plant viruses cannot transfect and deliver directly their genetic material or other cargos into mammalian cells. In this work, we prepared VLPs with the CCMV capsid and the mRNA-EGFP as a cargo and reporter gene. We show, for the first time, that these plant virus-based VLPs are capable of directly transfecting different eukaryotic cell lines, without the aid of any transfecting adjuvant, and delivering their nucleic acid for translation as observed by the presence of fluorescent protein. Our results show that the CCMV capsid is a good noncytotoxic container for genome delivery into mammalian cells.


1966 ◽  
Vol 164 (995) ◽  
pp. 230-245 ◽  

At this Symposium we are remembering and honouring the great and revolutionary discoveries of Gregor Mendel, presented to the world 100 years ago this year, which for the first time expressed the basic phenomena of heredity in a concise, analytical and, above all, numerical form and thus laid the foundation of the science of genetics. However, as the title of this symposium implies, we are not met here merely in adulation of Mendel’s genius but rather to review and discuss the fruits which have now matured on the tree which he planted. I think some of these fruits would seem very strange and incomprehensible to Mendel, for over the last two decades we have witnessed another revolution in genetics as dramatic and as pregnant with new potentialities as that of 100 years ago. The basic ingredients of this revolution were, first, the disclosure of systems of genetic recombination in micro-organisms, and especially in bacteria and their viruses, which enormously increased the resolution of genetic analysis; and, secondly, the elucidation by Watson & Crick, in 1953, of the physico-chemical structure of the genetic material, deoxyribonucleic acid—undoubtedly the most important and provocative biological discovery since Mendel. As a result we are now recapitulating the cytogenetical studies and correlations which marked the turn of the century, but this time the precision and refinement of our tools and techniques have increased more than 1000-fold so that we are looking at genetic behaviour and interaction at the level of molecular structure. In this lecture I would like to discuss what, from the Mendelian viewpoint, must be one of the most bizarre forms of sexual heredity, namely, the process of conjugation and genetic recombination in the bacterium Escherichia coli . My reasons for choosing this rather esoteric topic, apart from personal interest, are three. First, the whole mechanism of sexuality in this organism is mediated and controlled by a new kind of genetic element called the sex factor which, like some temperate bacteriophages, is able to exist in alternative states in the cell, either free in the cytoplasm or as an integral part of the bacterial chromosome, and which can properly be construed as a virus with a novel mode of infectivity, as I hope to show. Secondly, a number of essentially similar elements have recently been discovered in bacteria, masquerading under such different disguises as the genetic determinants of antibiotic substances called colicins or as carriers of transmissible drug resistance, so that the sex factor is far from being a unique entity among the bacteria. Thirdly, genetic interactions occur between the sex factor and the bacterial chromosome which confer great flexibility on this system. Some of the situations which are generated by these interactions mimic those found in the cells of higher organisms so that it is possible to construct plausible, though very speculative, models for the evolution of more stable and highly organized genetic systems.


2018 ◽  
Vol 10 (7) ◽  
pp. 1745-1764 ◽  
Author(s):  
Matthieu Leobold ◽  
Annie Bézier ◽  
Apolline Pichon ◽  
Elisabeth A Herniou ◽  
Anne-Nathalie Volkoff ◽  
...  

2020 ◽  
Author(s):  
Jérémy Gauthier ◽  
Hélène Boulain ◽  
Joke J.F.A. van Vugt ◽  
Lyam Baudry ◽  
Emma Persyn ◽  
...  

AbstractMost endogenous viruses, an important proportion of eukaryote genomes, are doomed to slowly decay. Little is known, however, on how they evolve when they confer a benefit to their host. Bracoviruses are essential for the parasitism success of parasitoid wasps, whose genomes they integrated ~103 million years ago. Here we show, from the assembly of a parasitoid wasp genome, for the first time at a chromosomal scale, that symbiotic bracovirus genes spread to and colonized all the chromosomes. Moreover, large viral clusters are stably maintained suggesting strong evolutionary constraints. Genomic comparison with another wasps revealed that this organization was already established ~53 mya. Transcriptomic analyses highlight temporal synchronization of viral gene expression, leading to particle production. Immune genes are not induced, however, indicating the virus is not perceived as foreign by the wasp. This recognition suggests that no conflicts remain between symbiotic partners when benefits to them converge.


PLoS ONE ◽  
2021 ◽  
Vol 16 (12) ◽  
pp. e0258311
Author(s):  
Diana S. Vargas-Bermudez ◽  
Santiago Rendon-Marin ◽  
Julian Ruiz-Saenz ◽  
Dario Mogollón ◽  
Jairo Jaime

There are a wide variety of porcine parvoviruses (PPVs) referred to as PPV1 to PPV7. The latter was discovered in 2016 and later reported in some countries in America, Asia, and Europe. PPV7 as a pathogenic agent or coinfection with other pathogens causing disease has not yet been determined. In the present study, we report the identification of PPV7 for the first time in Colombia, where it was found retrospectively since 2015 in 40% of the provinces that make up the country (13/32), and the virus was ratified for 2018 in 4/5 provinces evaluated. Additionally, partial sequencing (nucleotides 380 to 4000) was performed of four Colombian strains completely covering the VP2 and NS1 viral genes. A sequence identity greater than 99% was found when comparing them with reference strains from the USA and China. In three of the four Colombian strains, an insertion of 15 nucleotides (five amino acids) was found in the PPV7-VP2 capsid protein (540–5554 nt; 180–184 aa). Based on this insertion, the VP2 phylogenetic analysis exhibited two well-differentiated evolutionarily related groups. To evaluate the impact of this insertion on the structure of the PPV7-VP2 capsid protein, the secondary structure of two different Colombian strains was predicted, and it was determined that the insertion is located in the coil region and not involved in significant changes in the structure of the protein. The 3D structure of the PPV7-VP2 capsid protein was determined by threading and homology modeling, and it was shown that the insertion did not imply a change in the shape of the protein. Additionally, it was determined that the insertion is not involved in suppressing a potential B cell epitope, although the increase in length of the epitope could affect the interaction with molecules that allow a specific immune response.


Sign in / Sign up

Export Citation Format

Share Document