scholarly journals Effect of Nora virus infection on native gut bacterial communities of Drosophila melanogaster

2021 ◽  
Vol 7 (2) ◽  
pp. 216-237
Author(s):  
Makayla Schissel ◽  
◽  
Rebecca Best ◽  
Shelby Liesemeyer ◽  
Yuan-De Tan ◽  
...  
2018 ◽  
Vol 4 (1) ◽  
pp. 123-139 ◽  
Author(s):  
Wilfredo Lopez ◽  
◽  
Alexis M. Page ◽  
Darby J. Carlson ◽  
Brad L. Ericson ◽  
...  

2013 ◽  
Vol 175 (2) ◽  
pp. 95-100 ◽  
Author(s):  
Ethan J. Cordes ◽  
Kellie D Licking-Murray ◽  
Kimberly A. Carlson

Scientifica ◽  
2020 ◽  
Vol 2020 ◽  
pp. 1-6 ◽  
Author(s):  
Abigail Rogers ◽  
Lesley Towery ◽  
Amanda McCown ◽  
Kimberly A. Carlson

Nora virus (NV) is a picorna-like virus that contains a positive-sense, single-stranded RNA genome. The virus infects Drosophila melanogaster with no known characterized phenotype. In this study, geotaxis assays and longevity analyses were used to determine if Nora virus infection affects D. melanogaster’s locomotor ability. In addition, Drosophila C virus (DCV), a well-characterized D. melanogaster virus, was used as a positive control, as it has previously shown a locomotor defect in infected flies. Stocks infected with NV (NV+) and DCV (DCV+) and virus-free (NV-/DCV-) stocks were established. Over a 3-year period, approximately 2,500 virgin female flies were tested for geotaxis and longevity using Kaplan–Meier analyses, as well as the Cox Proportional Hazards regression for survivorship. There was a significant decrease in the geotaxis when the D. melanogaster flies were infected with Nora virus compared to uninfected controls, but no difference was found between DCV+ and NV+ trials. There were not significant differences in longevity between the three groups. This is the first time that a phenotype has been recorded in association with Nora virus infection. Overall, the data demonstrate that geotaxis dysfunction may be a phenotypic hallmark of Nora virus infection.


PLoS ONE ◽  
2016 ◽  
Vol 11 (12) ◽  
pp. e0167726 ◽  
Author(s):  
Mariia Chaplinska ◽  
Sylvia Gerritsma ◽  
Francisco Dini-Andreote ◽  
Joana Falcao Salles ◽  
Bregje Wertheim

2020 ◽  
Vol 48 (5) ◽  
pp. 2101-2115
Author(s):  
Beverly V. Robinson ◽  
Victor Faundez ◽  
Dorothy A. Lerit

Microcephaly is a rare, yet devastating, neurodevelopmental condition caused by genetic or environmental insults, such as the Zika virus infection. Microcephaly manifests with a severely reduced head circumference. Among the known heritable microcephaly genes, a significant proportion are annotated with centrosome-related ontologies. Centrosomes are microtubule-organizing centers, and they play fundamental roles in the proliferation of the neuronal progenitors, the neural stem cells (NSCs), which undergo repeated rounds of asymmetric cell division to drive neurogenesis and brain development. Many of the genes, pathways, and developmental paradigms that dictate NSC development in humans are conserved in Drosophila melanogaster. As such, studies of Drosophila NSCs lend invaluable insights into centrosome function within NSCs and help inform the pathophysiology of human microcephaly. This mini-review will briefly survey causative links between deregulated centrosome functions and microcephaly with particular emphasis on insights learned from Drosophila NSCs.


2021 ◽  
Vol 4 (1) ◽  
Author(s):  
Rodrigo Cogni ◽  
Shuai Dominique Ding ◽  
André C. Pimentel ◽  
Jonathan P. Day ◽  
Francis M. Jiggins

AbstractWolbachia is a maternally transmitted bacterial symbiont that is estimated to infect approximately half of arthropod species. In the laboratory it can increase the resistance of insects to viral infection, but its effect on viruses in nature is unknown. Here we report that in a natural population of Drosophila melanogaster, individuals that are infected with Wolbachia are less likely to be infected by viruses. By characterising the virome by metagenomic sequencing and then testing individual flies for infection, we found the protective effect of Wolbachia was virus-specific, with the prevalence of infection being up to 15% greater in Wolbachia-free flies. The antiviral effects of Wolbachia may contribute to its extraordinary ecological success, and in nature the symbiont may be an important component of the antiviral defences of insects.


2018 ◽  
Vol 93 (3) ◽  
Author(s):  
William H. Palmer ◽  
Joep Joosten ◽  
Gijs J. Overheul ◽  
Pascal W. Jansen ◽  
Michiel Vermeulen ◽  
...  

ABSTRACTInteractions between the insect immune system and RNA viruses have been extensively studied inDrosophila, in which RNA interference, NF-κB, and JAK-STAT pathways underlie antiviral immunity. In response to RNA interference, insect viruses have convergently evolved suppressors of this pathway that act by diverse mechanisms to permit viral replication. However, interactions between the insect immune system and DNA viruses have received less attention, primarily because fewDrosophila-infecting DNA virus isolates are available. In this study, we used a recently isolated DNA virus ofDrosophila melanogaster, Kallithea virus (KV; familyNudiviridae), to probe known antiviral immune responses and virus evasion tactics in the context of DNA virus infection. We found that fly mutants for RNA interference and immune deficiency (Imd), but not Toll, pathways are more susceptible to Kallithea virus infection. We identified the Kallithea virus-encoded protein gp83 as a potent inhibitor of Toll signalling, suggesting that Toll mediates antiviral defense against Kallithea virus infection but that it is suppressed by the virus. We found that Kallithea virus gp83 inhibits Toll signalling through the regulation of NF-κB transcription factors. Furthermore, we found that gp83 of the closely related Drosophila innubila nudivirus (DiNV) suppressesD. melanogasterToll signalling, suggesting an evolutionarily conserved function of Toll in defense against DNA viruses. Together, these results provide a broad description of known antiviral pathways in the context of DNA virus infection and identify the first Toll pathway inhibitor in aDrosophilavirus, extending the known diversity of insect virus-encoded immune inhibitors.IMPORTANCECoevolution of multicellular organisms and their natural viruses may lead to an intricate relationship in which host survival requires effective immunity and virus survival depends on evasion of such responses. Insect antiviral immunity and reciprocal virus immunosuppression tactics have been well studied inDrosophila melanogaster, primarily during RNA, but not DNA, virus infection. Therefore, we describe interactions between a recently isolatedDrosophilaDNA virus (Kallithea virus [KV]) and immune processes known to control RNA viruses, such as RNA interference (RNAi) and Imd pathways. We found that KV suppresses the Toll pathway and identified gp83 as a KV-encoded protein that underlies this suppression. This immunosuppressive ability is conserved in another nudivirus, suggesting that the Toll pathway has conserved antiviral activity against DNA nudiviruses, which have evolved suppressors in response. Together, these results indicate that DNA viruses induce and suppress NF-κB responses, and they advance the application of KV as a model to study insect immunity.


2021 ◽  
Author(s):  
Shaun T. Cross ◽  
Ali L Brehm ◽  
Tillie J Dunham ◽  
Case P Rodgers ◽  
Grace I Borlee ◽  
...  

Galbut virus (family Partitiviridae) infects Drosophila melanogaster and can be transmitted vertically from infected mothers or infected fathers with near perfect efficiency. This form of super-Mendelian inheritance should drive infection to 100% prevalence, and indeed galbut virus is ubiquitous in wild D. melanogaster populations. But on average only about 60% of individual flies are infected. One possible explanation for this apparent paradox is that a subset of flies are resistant to infection. Although galbut virus infected flies seem healthy, infection may be sufficiently costly to drive selection for resistant hosts, thereby decreasing overall prevalence. To test this hypothesis, we quantified a variety of fitness-related traits in galbut virus infected flies from two lines from the Drosophila Genetic Reference Panel (DGRP). Galbut virus infected flies had slightly decreased average lifespan and total offspring production, but these decreases were mostly not statistically significant. Galbut virus DGRP-517 flies pupated and eclosed slightly faster than their uninfected counterparts. Some galbut virus infected flies exhibited altered sensitivity to viral, bacterial, and fungal pathogens. Galbut virus infection produced minimal changes to host mRNA levels as measured by RNA sequencing, consistent with minimal phenotypic changes. The microbiome composition of flies was not measurably perturbed by galbut virus infection. Differences in phenotype attributable to galbut virus infection varied as a function of fly sex and DGRP strain and were generally dwarfed by larger differences attributable to strain and sex. Thus, galbut virus infection does produce measurable phenotypic changes, with changes being minor, offsetting, and possibly net negative


Virology ◽  
2008 ◽  
Vol 377 (1) ◽  
pp. 197-206 ◽  
Author(s):  
Heather L. Chotkowski ◽  
Alexander T. Ciota ◽  
Yongqing Jia ◽  
Francesc Puig-Basagoiti ◽  
Laura D. Kramer ◽  
...  

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