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TWiV 431: Niemann-Pick of the weak

5 March 2017 by Vincent Racaniello

The TWiVirions reveal bacteriophage genes that control eukaryotic reproduction, and the biochemical basis for increased Ebolavirus glycoprotein activity during the recent outbreak.

You can find TWiV #431 at microbe.tv/twiv, or listen below.

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Filed Under: This Week in Virology Tagged With: arthropod, bacteriophage, cytoplasmic incompatibility, ebolavirus, glycoprotein, mutation, Niemann-Pick C1, prophage, selection, transmission, viral, virology, virus, WO, wolbachia

A virus that controls reproduction

3 March 2017 by Vincent Racaniello

WolbachiaThe obligate intracellular bacteria Wolbachia (pictured), which infects 40% of arthropods, can manipulate its host to ensure its maintenance in the population. An example is cytoplasmic incompatibility, which occurs when infected males mate with uninfected females, and causes embryonic lethality (mating with an infected female produces viable offspring). Two Wolbachia genes responsible for this phenotype have been identified, and they are viral (link to paper).

A comparison of genome sequences of different Wolbachia strains that do or do not cause cytoplasmic incompatibility (CI) revealed two genes that were candidates for this phenotype. Both genes are transcribed in the testes of fruit flies, but at lower levels in older male flies which show decreased CI.

When either gene was expressed in male transgenic fruit flies, there was no effect on hatch rates after mating with uninfected females. When both genes were expressed in male flies, mating with uninfected females led to substantially reduced hatch rates. This transgene-induced lethality was rescued when the flies were mated with Wolbachia-infected females.

The two genes that together cause CI are called cytoplasmic incompatibility factor A and B (cifA, cifB). The cytological defects caused by these genes resemble those observed in Wolbachia-induced CI: most embryos do not divide more than two or three times.

Remarkably (or perhaps not!), cifA and cifB are not Wolbachia genes, but are viral. Wolbachia are infected with a bacteriophage called WO; nearly all sequenced Wolbachia genomes contain integrated WO DNA, and it is within this WO prophage that are found cifA and cifB. In other words, the ability of Wolbachia to control the reproduction of its arthropod host is regulated by two viral genes integrated in the bacterial genome.

Because CI caused by Wolbachia is a means of increasing their proportion in the female line (the bacteria are maternally inherited), cifA and cifB also enable spread of WO bacteriophage.

How cifA and cifB cause CI is unknown – most of the encoded proteins have no recognized protein domains with the exception of weak homology to proteases.  Understanding this mechanism might also contribute to controlling the spread of arboviruses: Wolbachia is known to inhibit replication of some mosquito borne viruses such as dengue virus and Zika virus.

Filed Under: Basic virology, Information Tagged With: arthropod, bacteriophage, cytoplasmic incompatibility, lysogen, prophage, viral, virology, virus, WO, wolbachia

Virus Watch: How mosquitoes spread viruses

9 June 2016 by Vincent Racaniello

In this episode of Virus Watch, I explain how mosquitoes spread viruses. We’ll look at how a mosquito finds a host, how it finds a blood vessel, and how it delivers viruses to a new host. Don’t blame mosquitoes for viral diseases: it’s not their fault!

Filed Under: Virus Watch Tagged With: arbovirus, arthropod, blood meal, mosquito, transmission, vector, video, viral, virology, virus, viruses, zika virus

TWiP 41: Flying and crawling beasts

27 June 2012 by Vincent Racaniello

On episode #41 of the science show This Week in Parasitism, Vincent and Dickson review medically important arthropods.

You can find TWiP #41 at microbeworld.org/twip.

Filed Under: This Week in Parasitism Tagged With: arachnid, arthropod, insect, parasite, parasitism, This Week in Parasitism, twip, vector

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by Vincent Racaniello

Earth’s virology Professor
Questions? virology@virology.ws

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