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First Preliminary Profile of Proteins in Bed Bugs' Saliva

July 12, 2010 — With bed bugs reemerging as a nuisance in some parts of the country, scientists are reporting the first preliminary description of the bug's sialome -- the saliva proteins that are the secret to Cimex lectularius' ability to suck blood from its human victims and escape to bite again with risking a lethal slap. The findings, which could have medical applications in diagnosing bed bug bites and preventing the itch, appear in ACS' monthly Journal of Proteome Research.


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In the report, Jose Ribeiro and colleagues point out that bed bugs have made reappearances in New York City, London, and other areas, sparking increased scientific interest in the allergic responses associated with their bites. Bed bugs belong to a group of insects that feed on blood throughout their lives and have been doing so successfully for at least 250 million years. That success depends in large part on proteins in their saliva, substances that make the victim's blood vessels dilate (for a better flow of blood), inhibit clotting, and prevent immediate pain and itching that might evoke a lethal slap.

Using adult bed bugs from a government-maintained colony, the scientists removed salivary glands from male and female bugs, and analyzed the proteins to find unique enzymes that characterize the saliva profile of the bug. The substances could also offer insight into how insects evolved to a blood diet. "Independent of their function, these proteins may also be used for immune detection of humans and animals to bed bug exposure, or as part of desensitization vaccines," the report says.

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The above story is reprinted from materials provided by American Chemical Society, via EurekAlert!, a service of AAAS.

Note: Materials may be edited for content and length. For further information, please contact the source cited above.


Journal Reference:

  1. Francischetti et al. Insight into the Sialome of the Bed Bug, Cimex lectularius. Journal of Proteome Research, 2010; 100519110228027 DOI: 10.1021/pr1000169
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