“…We designed an assay to test larvae for their ability to stop bleeding, and differences were found between the feeding and wandering stages of third instar larvae that correlated with differences in the number of circulating hemocytes at the different stages (Chang et al, 2012). Using this assay, fewer hmlf03374 larvae survived when wounded in the feeding stage of the third larval instar (Chang et al, 2012). Still, most wounded hmlf03374 larvae survived.…”
Section: Coagulation Study In Vivomentioning
confidence: 98%
“…This suggested that while fon MB11923 had a greater effect than RNAi knockdown, the larvae still retain some residual fon coagulation function. In addition, we compared wildtype larvae in the feeding and wandering stages and demonstrated that like wound survival (Chang et al, 2012), hemolymph from different stage larvae showed different strand lengths. Significant differences were found between each group (P < 0.05 by t test) indicated by asterisks, while the difference between fon MB11923 and fon MB11923 /Df was highly significant (P < 0.01) as indicated by double asterisks.…”
Section: Fon Rescue: Fond 17a and Fond 27amentioning
confidence: 99%
“…Significantly longer strands could be drawn from the hemolymph of wild type feeding stage larvae than from the hemolymph of wandering stage larvae. The latter have more hemocytes in circulation (Chang et al, 2012), and hence are able to form a denser, more brittle clot, leading to strands breaking earlier, at shorter lengths in the spaghetti assay.…”
Section: Fon Mb11923mentioning
confidence: 99%
“…Feeding stage larvae were isolated using blue food as described in (Chang et al, 2012). Briefly, larvae were kept on medium with 0.5% bromophenol blue, and third instar feeding stage larvae were identified by their visibly blue guts.…”
Section: Larval Stagingmentioning
confidence: 99%
“…The wounding assay was described in (Chang et al, 2012). Briefly, feeding stage larvae were isolated from blue food vials, washed in deionized water, and gently dried with tissue.…”
“…We designed an assay to test larvae for their ability to stop bleeding, and differences were found between the feeding and wandering stages of third instar larvae that correlated with differences in the number of circulating hemocytes at the different stages (Chang et al, 2012). Using this assay, fewer hmlf03374 larvae survived when wounded in the feeding stage of the third larval instar (Chang et al, 2012). Still, most wounded hmlf03374 larvae survived.…”
Section: Coagulation Study In Vivomentioning
confidence: 98%
“…This suggested that while fon MB11923 had a greater effect than RNAi knockdown, the larvae still retain some residual fon coagulation function. In addition, we compared wildtype larvae in the feeding and wandering stages and demonstrated that like wound survival (Chang et al, 2012), hemolymph from different stage larvae showed different strand lengths. Significant differences were found between each group (P < 0.05 by t test) indicated by asterisks, while the difference between fon MB11923 and fon MB11923 /Df was highly significant (P < 0.01) as indicated by double asterisks.…”
Section: Fon Rescue: Fond 17a and Fond 27amentioning
confidence: 99%
“…Significantly longer strands could be drawn from the hemolymph of wild type feeding stage larvae than from the hemolymph of wandering stage larvae. The latter have more hemocytes in circulation (Chang et al, 2012), and hence are able to form a denser, more brittle clot, leading to strands breaking earlier, at shorter lengths in the spaghetti assay.…”
Section: Fon Mb11923mentioning
confidence: 99%
“…Feeding stage larvae were isolated using blue food as described in (Chang et al, 2012). Briefly, larvae were kept on medium with 0.5% bromophenol blue, and third instar feeding stage larvae were identified by their visibly blue guts.…”
Section: Larval Stagingmentioning
confidence: 99%
“…The wounding assay was described in (Chang et al, 2012). Briefly, feeding stage larvae were isolated from blue food vials, washed in deionized water, and gently dried with tissue.…”
Insect models, such as Galleria mellonella and Drosophila melanogaster have significant ethical, logistical, and economic advantages over mammalian models for the studies of infectious diseases. Using these models, various pathogenic microbes have been studied and many novel virulence genes have been identified. Notably, because insects are susceptible to a wide variety of human pathogens and have immune responses similar to those of mammals, they offer the opportunity to understand innate immune responses against human pathogens better. It is important to note that insect pathosystems have also offered a simple strategy to evaluate the efficacy and toxicity of many antimicrobial agents. Overall, insect models provide a rapid, inexpensive, and reliable way as complementary hosts to conventional vertebrate animal models to study pathogenesis and antimicrobial agents.
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