Pyrethroid resistance in cockroach populations has been a public health challenge since the 1950s. The pyrethroid resistance in the German cockroach, Blattella germanica, is primarily attributed to knockdown resistance (kdr) mutations (E434K, C764R, and L993F) in the voltage-sensitive sodium channel gene (vssc). In this study, the pyrethroid resistance state of the German cockroach in the Republic of Korea (ROK) was assessed by analyzing the frequencies of kdr mutations using one-step PCR with total RNA. The results revealed that among the 25 populations examined, 14 populations exhibited the L993F kdr mutation, while no other mutations were detected. Since other cockroach species are also commonly found in human dwellings in ROK, the vssc genes were cloned from four other species, including Blattella nipponica, Periplaneta americana, Periplaneta japonica, and Periplaneta fuliginosa. Based on the genomic DNA (gDNA) sequences obtained from the vssc cloning, primer sets were designed to amplify the vssc fragment spanning the L993F mutation for each species and used to monitor the development of pyrethroid resistance in cockroach populations in the ROK. The study will facilitate the implementation of a nationwide monitoring program to assess cockroach resistance and select suitable alternatives.

The functional cardiovascular system is comprised of distinct mesoderm-derived lineages including endothelial cells, vascular smooth muscle cells and other mesenchymal cells. Recent studies in the human embryonic stem cell differentiation model have provided evidence indicating that these cell lineages are developed from the common progenitors such as hemangioblasts and cardiovascular progenitor cells. Also, the studies have suggested that these progenitors have a common primordial progenitor, which expresses KDR (human Flk-1, also known as VEGFR2, CD309). We demonstrate here that sustained activation of BMP4 (bone morphogenetic protein 4) in hESC line, CHA15 hESC results in KDR+ mesoderm specific differentiation. To determine whether the KDR+ population derived from hESCs enhances potential to differentiate along multipotential mesodermal lineages than undifferentiated hESCs, we analyzed the development of the mesodermal cell types in human embryonic stem cell differentiation cultures. In embryoid body (EB) differentiation culture conditions, we identified an increased expression of KDR+ population from BMP4-stimulated hESC-derived EBs. After induction with additional growth factors, the KDR+ population sorted from hESCs-derived EBs displays mesenchymal, endothelial and vascular smooth muscle potential in matrix-coated monolayer culture systems. The populations plated in monolayer cultures expressed increased levels of related markers and exhibit a stable/homologous phenotype in culture terms. In conclusion, we demonstrate that the KDR+ population is stably isolated from CHA15 hESC-derived EBs using BMP4 and growth factors, and sorted KDR+ population can be utilized to generate multipotential mesodermal progenitors in vitro, which can be further differentiated into cardiovascular specific cells.