When two species, be they large seabirds and their parasites or tiny bacteria and their viral enemies, share an environment over evolutionary time, they are said to co-evolve. This simply means that they have learned how to deal with each other. Sometimes different species learn to peacefullycoexist (and even help each other), but less friendly interactions are also common.Thiskind of feuding leads to the constant development by each species of new strategies for taking advantage of its enemies, or for defending itself.Recently, researchers have adapted some of these ancient biological tricks, such as CRISPR, to be wieldedagainst the diseases that currently plague us.
Matteo Farinella
A powerful genome editing technology, CRISPRallows researchers to alter DNA sequences, and has becomea versatile tool of modern molecular biology and medicine.Butlong before humans developed this technology, CRISPR systems naturallyevolved in bacteria as antiviral immune responses. It seems fitting,therefore, that some of the most promising applications for CRISPR are developingantiviral therapies.
Recently, Americanresearchers successfully used CRISPR to eliminate HIV in mice. HIV is a retrovirus a type of virus that inserts copies of its own genetic code into the genomes of the cells that it infects. An existing HIV treatment, LASER ART (which stands for long-acting slow effective release antiretroviral therapy), isvery effective at stopping the production and insertion of new copies of the virus, but itcan't remove genetic codethat has already been created. In other words, modern therapies can stop the HIV infection from spreading, but cant eliminate it entirely. That's whyHIV is considereda chronic disease that requires lifelong treatment.
A permanent cure for HIV (and other retroviral diseases) would require removing or inactivating the viral DNA that is mixed with the hosts own genome. Conveniently, cutting through unwanted DNA sequences is CRISPRs specialty.
Inbacteria infected by viruses in natural conditions,special enzymes recognizethe intrusion of foreign DNA.They use that DNA as a template to produce guide RNAs, whichCas9, a DNA-cutting enzyme, can use to find its intended targets. The next time a bacterium encounters this foreign DNA,Cas9 can recognize and destroy it. This protects the bacterium from repeated infection by the same viruses.
With CRISPR, scientistscan use artificially-createdguide RNAs to direct Cas9 to the targets they're interested in. In this particular HIV study,after suppressingthe HIVinfection with LASER ART, the researchers treated the mice with edited guide RNAs that excised the viral DNA from the genome actually "curing" the mice of the chronic disease.
Although this approach is incredibly promising, an important caveat is that the editing worked in less than half the mice.
Rama on Wikimedia Commons
Although this approach is incredibly promising, an important caveat is that the editing worked inless than half the mice. The excision of the viral DNA was incomplete in the rest. It is plausible that theexcision efficiency could be improved by increasing the duration of CRISPR-Cas9 treatment. But a worrying possibility is that the HIV virus will quickly develop mutations that help it avoid detection by the synthetic guide RNA. This exact scenario was encountered in a recent attempt to use a similar CRISPR technique to protect the food crop cassava from gemini viruses (note: the lead author of this cassava study, Devang Mehta, is a Massive contributor). Native bacterial CRISPR systems would naturally develop new guide RNAs to combat the new viral strains. But for use in mice, cassava, or humans, scientistsmight find themselves forced to constantly re-engineer synthetic guides, or to use multiple guides for simultaneous targeting of different parts of the viral genes.
We've seen similar arms races with other types of medical treatments derived from natural sources. The first modern antibiotic, penicillin, was isolated from a mold. Many clinically-useful antibacterial agents have since been isolated from microbes but the problem of antibacterial resistance is growing.Whenconventional antibiotics fail, doctors have recently started turning toviruses that can be used tospecifically target bacteria to fight off infection, a strategy known as phage therapy.
This demonstration of CRISPR as an antiviral therapy may be among the first of many but it is part of a longstanding trend of borrowing tools from simple organisms for our own battles.
More:
Researchers use CRISPR to eliminate HIV in mice, DNA and all - Massive Science
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