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  1. Naked Science Forum
  2. Profile of Candy Swift
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Pages: [1]
1
General Science / Can trojan bacteria be used to conquer Sleeping Sickness?
« on: 13/11/2015 06:23:33 »
Sleeping sickness caused by trypanosoma brucei can be transmitted to other people or animals through by tsetse flies. According to a new research paper published on the open-access journal Microbial Cell Factories by BioMed Central on February 15, 2012, researchers use a kind of nanobodies released by tsetse flies under natural environment to defense against these trypanosomata, which means that this kind of nanobodies play a similar role as Trojan horses. They are the first step in making specific nanobodies that can kill or stunt the growth of trypanosomata.

Sleeping sickness threatens millions of lives living in sub-Saharan Africa. In the first stage (hemolymph stage) of trypanosoma brucei infection, its symptoms are fever, headache, joint pain and itching. After this parasite infection across the BBB and enters the second stage (nerves stage), it leads to thoughts confusion, poor coordination and sleep disorders. This disease is fatal without timely treatment. The diagnosis and treatment of this disease, however, are not easy. Only those who have received special training can handle. After infected by trypanosome, bovines can be anemic and may even die from anemia. The comprehensive conclusion is that trypanosomata have brought serious negative effect to public health and agricultural development throughout the African continent.

Sodalis glossinidius are internal symbiotic bacteria that are similar to beneficial bacteria settled in our intestine. Theycan be found in the midgut, muscle, fat and salivary glands of tsetse flies. As female tsetse will pass these bacteria to their offsprings, the genetically modified bacteria should be able to pass down from one generation to another once these female flies are released in the wild.

Professor Van Den Abbeele, an expert from Antwerp Institute of Tropical Diseases, explained, “When we study live trypanosomes inside the simulated intestine of tsetse, we found that these genetically modified bacterium expressed nanobodies have biological activity and can bind to the entire surface of the parasite. Since we know that this technology is effective, we are now studying these nanobodies that can damage or block the development of this type of parasites in tsetse intestine. “

Epidemic Sleeping sickness of these years first appeared in the 1970s. Although we have been trying to decline the number of new cases in the past 10 years, this disease has not yet been eradicated. This new technology gives people hope to fight against this devastating disease.

Article Title: Trojan Bacteria Conquer Sleeping Sickness with Nanobody

2
That CAN'T be true! / A New Gene Has Been Found to Restrain the Spread of AIDS Virus?
« on: 09/11/2015 06:29:23 »
It is reported that some researchers from KCL have found a new gene named MX2, which can restrain the spread of AIDS virus to a large degree. Those researchers said the discovery of this unique gene function will pave the way for developing more effective and less toxic treatments in AIDS. Relevant studies have been published in the latest issue of Nature.

We often hear reports say that which certain gene or technique was discovered or created to restrain AIDs, but the fact is that we've never seen a real one that can accomplish this "dream task". Will you still believe in this new gene mention in the article?

The article source: A New Gene Has Been Found to Restrain the Spread of AIDS Virus

3
General Science / How are proteins expressed in bacteria?
« on: 26/10/2015 08:38:40 »
How to conduct protein expression in bacteria? I searched the internet, and learned that The first choice for the expression of recombinant proteins is typically E. coli. Production of proteins in this bacterial strain is well-established, fast and simple and usually provides high yields. Recent progress in the fundamental understanding of transcription, translation, and protein folding in E. coli, improved genetic tools had made this bacterium more valuable than ever for the expression of complex eukaryotic proteins.

Can anyone show me more? Thanks!

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