Insecticide-impregnated nets can kill triatomine bugs, but it remains unclear whether they can protect against Chagas disease transmission. In a field trial in Quequeña, Peru, sentinel guinea pigs placed in intervention enclosures covered by deltamethrin-treated nets showed significantly lower antibody responses to saliva of Triatoma infestans compared with animals placed in pre-existing control enclosures. Our results strongly suggest that insecticide-treated nets prevent triatomine bites and can thereby protect against infection with Trypanosoma cruzi. Anti-salivary immunoassays are powerful new tools to evaluate intervention strategies against Chagas disease.

• MeSH
• Chagasova nemoc prevence a kontrola   MeSH
• dezinsekce metody   MeSH
• imunoanalýza MeSH
• kousnutí a bodnutí hmyzem imunologie   prevence a kontrola   MeSH
• morčata MeSH
• parazitologie metody   MeSH
• sítě nad lůžka napuštěné insekticidy MeSH
• sliny imunologie   MeSH
• Triatoma imunologie   MeSH
• zvířata MeSH
• Check Tag
• morčata MeSH
• mužské pohlaví MeSH
• ženské pohlaví MeSH
• zvířata MeSH
• Publikační typ
• časopisecké články MeSH
• práce podpořená grantem MeSH
• Research Support, N.I.H., Extramural MeSH
• Geografické názvy
• Peru MeSH

We have previously demonstrated that two salivary cysteine protease inhibitors from the Borrelia burgdorferi (Lyme disease) vector Ixodes scapularis- namely sialostatins L and L2 - play an important role in tick biology, as demonstrated by the fact that silencing of both sialostatins in tandem results in severe feeding defects. Here we show that sialostatin L2 - but not sialostatin L - facilitates the growth of B. burgdorferi in murine skin. To examine the structural basis underlying these differential effects of the two sialostatins, we have determined the crystal structures of both sialostatin L and L2. This is the first structural analysis of cystatins from an invertebrate source. Sialostatin L2 crystallizes as a monomer with an 'unusual' conformation of the N-terminus, while sialostatin L crystallizes as a domain-swapped dimer with an N-terminal conformation similar to other cystatins. Deletion of the 'unusual' N-terminal five residues of sialostatin L2 results in marked changes in its selectivity, suggesting that this region is a particularly important determinant of the biochemical activity of sialostatin L2. Collectively, our results reveal the structure of two tick salivary components that facilitate vector blood feeding and that one of them also supports pathogen transmission to the vertebrate host.

• MeSH
• Borrelia burgdorferi patogenita   MeSH
• cystatiny chemie   izolace a purifikace   MeSH
• klíště chemie   mikrobiologie   MeSH
• lymeská nemoc přenos   MeSH
• molekulární modely MeSH
• molekulární sekvence - údaje MeSH
• myši inbrední C3H MeSH
• myši MeSH
• rekombinantní proteiny chemie   izolace a purifikace   MeSH
• sekvence aminokyselin MeSH
• sekvenční seřazení MeSH
• slinné cystatiny chemie   izolace a purifikace   MeSH
• terciární struktura proteinů MeSH
• zvířata MeSH
• Check Tag
• myši MeSH
• zvířata MeSH
• Publikační typ
• časopisecké články MeSH
• práce podpořená grantem MeSH
• Research Support, N.I.H., Intramural MeSH
• Research Support, U.S. Gov't, Non-P.H.S. MeSH