Inhibition of Chikungunya virus infection in cultured human muscle cells by furin inhibitors: impairment of the maturation of the E2 surface glycoprotein

Chikungunya virus (CHIKV) is a mosquito-transmitted Alphavirus that causes in humans an acute infection characterized by polyarthralgia, fever, myalgia, and headache. Since 2005 this virus has been responsible for an epidemic outbreak of unprecedented magnitude. By analogy with other alphaviruses, it is thought that cellular proteases are able to process the viral precursor protein E3E2 to produce the receptor-binding E2 protein that associates as a heterodimer with E1. Destabilization of the heterodimer by exposure to low pH allows viral fusion and infection. We show that among a large panel of proprotein convertases, membranous furin but also PC5B can process E3E2 from African CHIKV strains at the HRQRR(64) / ST site, whereas a CHIKV strain of Asian origin is cleaved at RRQRR(64) / SI by membranous and soluble furin, PC5A, PC5B, and PACE4 but not by PC7 or SKI-1. Using fluorogenic model peptides and recombinant convertases, we observed that the Asian strain E3E2 model peptide is cleaved most efficiently by furin and PC5A. This cleavage was also observed in CHIKV-infected cells and could be blocked by furin inhibitor decanoyl-RVKR-chloromethyl ketone. This inhibitor was compared with chloroquine for its ability to inhibit CHIKV spreading in myoblast cell cultures, a cell-type previously described as a natural target of this virus. Our results demonstrate the role of furin-like proteases in the processing of CHIKV particles and point out new approaches to inhibit this infection.     

The Pleistocene Ma U’Oi cave, northern Vietnam: palaeontology, sedimentology and palaeoenvironments

In November 2001, a Vietnamese-French team undertook the excavation of the Ma U’Oi cave in northern Vietnam. This limestone karst cave is located in the province of Hoà Binh, 70 km ESE from Hanoi and is typical of the northern Vietnam landscape. The site yielded an in situ mammalian fauna of a relatively modern composition. We also found a mixed fauna with a lower molar attributed to an archaic Homo(Demeter et al., in press). We estimate the age of Ma U’Oi fauna between 169 kyr, the age of Thum Wiman Nakin (Esposito et al., 1998) estimated by U/Th method and 80-60 kyr, the biochronological age of Lang Trang (Long et al., 1996), or even Holocene. The Ma U’Oi site is important because of the scarcity of Vietnamese sites of those particular levels. For that reason, it fills a gap in the biostratigraphy of Vietnam and permits new correlations with other sites of the mainland, especially those well documented from Thailand.     

Des chambres de pupation de Dermestidae (Insecta : Coleoptera) sur un os de mammifère tertiaire (phosphorites du Quercy) : implications taphonomiques et paléoenvironnementales

The larvae of some species of Dermestidae (Coleoptera) are able to bore the bones of a carrion for pupation. Several pupal chambers have been observed on an unciform belonging to a fossil rhinocerotid (Mesaceratherium sp.) from the late Oligocene/earliest Miocene of the phosphorites of Quercy (SW France). Such an unusual observation demonstrates the occurrence of dermestids in the entomofauna of the phosphorites of Quercy, and suggests at least the existence of paleoclimatic episodes with dry seasons, during a period usually considered as a relatively humid one. This is the earliest occurrence of such ichnofossils on a fossil mammal bone.     

Photo-crosslinking of proteins in intact cells reveals a dimeric structure of cyclooxygenase-2 and an inhibitor-sensitive oligomeric structure of microsomal prostaglandin E2 synthase-1

We have characterized the structures of cyclooxygenase-2 (COX-2) and microsomal prostaglandin E₂ synthase-1 (mPGES-1) in intact cells using bifunctional and photo-activatable crosslinking agents. A dimeric complex was detected for COX-2 by both crosslinking approaches, consistent with the crystal structure of the enzyme. For mPGES-1, treatment of A549 cells with disuccinimidyl suberate yielded immunoreactive protein bands corresponding to a dimer (33 kDa) and a trimer (45 kDa), as observed for the isolated enzyme. Photo-crosslinking with photoactivatable methionine in intact cells generated complexes with molecular weights corresponding to the dimer (33 kDa) and two putative trimer forms (50 and 55 kDa). Treatment with the selective mPGES-1 inhibitor MF63 prevented the formation of the 50 and 55 kDa crosslinked complexes, while an inactive structural analogue had no effect. Our data indicate that COX-2 forms a dimer in intact cells and that mPGES-1 has an oligomeric structure that can be disrupted by a selective inhibitor.     

CXXC domain of human DNMT1 is essential for enzymatic activity

DNA cytosine methylation is one of the major epigenetic gene silencing marks in the human genome facilitated by DNA methyltransferases. DNA cytosine-5 methyltransferase 1 (DNMT1) performs maintenance methylation in somatic cells. In cancer cells, DNMT1 is responsible for the aberrant hypermethylation of CpG islands and the silencing of tumor suppressor genes. Here we show that the catalytically active recombinant DNMT1, lacking 580 amino acids from the amino terminus, binds to unmethylated DNA with higher affinity than hemimethylated or methylated DNA. To further understand the binding domain of enzyme, we have used gel shift assay. We have demonstrated that the CXXC region (C is cysteine; X is any amino acid) of DNMT1 bound specifically to unmethylated CpG dinucleotides. Furthermore, mutation of the conserved cysteines abolished CXXC mediated DNA binding. In transfected COS-7 cells, CXXC deleted DNMT1 (DNMT1 (DeltaCXXC)) localized on replication foci. Both point mutant and DNMT1 (DeltaCXXC) enzyme displayed significant reduction in catalytic activity, confirming that this domain is crucial for enzymatic activity. A permanent cell line with DNMT1 (DeltaCXXC) displayed partial loss of genomic methylation on rDNA loci, despite the presence of endogenous wild-type enzyme. Thus, the CXXC domain encompassing the amino terminus region of DNMT1 cooperates with the catalytic domain for DNA methyltransferase activity.     

Middle Miocene elasmotheriine Rhinocerotidae from China and Mongolia: taxonomic revision and phylogenetic relationships

Eight elasmotheriine rhinocerotid species have been described from the Middle Miocene of China and Mongolia. In this paper a revised taxonomy is presented based on direct observation and comparison of the available material. A phylogenetic analysis based on 282 morphological characters has led to the reappraisal of Procoelodonta Matthew, 1931, Caementodon Heissig, 1972 and Huaqingtherium Huang & Yan, 1983. The genus Procoelodonta is split into three subgenera: P.  ( Procoelodonta ) Matthew, 1931, P.  ( Begertherium ) Beliaeva, 1971, and P.  ( Pasalarhinus subg. n). The genus Caementodon is split into two subgenera: C.  ( Caementodon ) Heissig, 1972 and C.  ( Beliajevina ) Heissig, 1974. Four species are assumed to have occurred in the Middle Miocene within the area studied: Procoelodonta ( Procoelodonta ) mongoliense (Osborn, 1924), ' P. ' ( Begertherium ) borissiaki (Beliaeva, 1971), ' Caementodon ' ( Beliajevina ) fangxianense (Yan, 1979) and Huaqingtherium lintungense (Zhai, 1978) (=' Caementodon tongxinensis ' Guan, 1988 =' Huaqingtherium qiui ' Guan, 1993 =' Hispanotherium tungurense ' Cerdeño, 1996). Shennongtherium hypsodontus Huang & Yan, 1983 is removed from the Elasmotheriina, owing to dental characters which suggest that it is a teleoceratine. The distribution of the main characters later seen in Elasmotherium is briefly discussed. The persistence and diversity of the Elasmotheriina throughout the Middle Miocene help explain how minute brachyodont animals gave rise to the mammoth-sized hypsodont Elasmotherium.     

Polypeptide components of the apamin receptor associated with a calcium activated potassium channel

Photoaffinity labeling of rat brain membranes with [125I]ANPAA-apamin incorporated radioactivity into polypeptides of 86 and 59 kDa and occasionally a more weakly labeled component of 45 kDa. These polypeptides were immunoprecipitated with anti-apamin antibodies and treated with glycosidases. Neither the 86 nor the 59 kDa polypeptide appeared to be N-glycosylated. Partial proteolytic mapping of affinity labeled polypeptides with chymotrypsin or V8 protease generated an identical pattern. These results suggest that the 59 and 45 kDa components are not additional subunits of an oligomeric protein but result from cleavage of the 86 kDa polypeptide.     

Anthropogenic disturbance induces opposing population trends in spotted hyenas and African lions

Large carnivore populations are declining worldwide due to direct and indirect conflicts with humans. Protected areas are critical for conserving large carnivores, but increasing human-wildlife conflict, tourism, and human population growth near these sanctuaries may have negative effects on the carnivores within sanctuary borders. Our goals were to investigate how anthropogenic disturbance along the edge of the Masai Mara National Reserve, Kenya, influences the demography and space-use of two large carnivore species that engage in intense interspecific competition. Here we document, in one disturbed region of the Reserve, a rapid increase in the population size of one large predator, the spotted hyena (Crocuta crocuta), but a striking concurrent decline in numbers of another, the African lion (Panthera leo). Anthropogenic disturbances negatively affected lion populations, and decreasing lion numbers appear to have a positive effect on hyena populations, indicated here by an increase in juvenile survivorship. We also saw an increase in the number of livestock consumed by hyenas. Our results suggest human population growth and indirect effects of human activity along Reserve boundaries may be effecting a trophic cascade inside the Reserve itself. These results indicate both top-down and bottom-up processes are causing a shift in the carnivore community, and a major disruption of guild structure, inside the boundaries of one of the most spectacular protected areas in Africa.     

Mrp1 Multidrug Resistance-Associated Protein and P-Glycoprotein Expression in Rat Brain Microvessel Endothelial Cells

Abstract: Two membrane glycoproteins acting as energy-dependent efflux pumps, mdr -encoded P-glycoprotein (P-gp) and the more recently described multidrug resistance-associated protein (MRP), are known to confer cellular resistance to many cytotoxic hydrophobic drugs. In the brain, P-gp has been shown to be expressed specifically in the capillary endothelial cells forming the blood-brain barrier, but localization of MRP has not been well characterized yet. Using RT-PCR and immunoblot analysis, we have compared the expression of P-gp and Mrp1 in homogenates, isolated capillaries, primary cultured endothelial cells, and RBE4 immortalized endothelial cells from rat brain. Whereas the mdr1a P-gp-encoding mRNA was specifically detected in brain microvessels and mdr1b mRNA in brain parenchyma, mrp1 mRNA was present both in microvessels and in parenchyma. However, Mrp1 was weakly expressed in microvessels. Mrp1 expression was higher in brain parenchyma, as well as in primary cultured brain endothelial cells and in immortalized RBE4 cells. This Mrp1 overexpression in cultured brain endothelial cells was less pronounced when the cells were cocultured with astrocytes. A low Mrp activity could be demonstrated in the endothelial cell primary monocultures, because the intracellular [³H]vincristine accumulation was increased by several MRP modulators. No Mrp activity was found in the cocultures or in the RBE4 cells. We suggest that in rat brain, Mrp1, unlike P-gp, is not predominantly expressed in the blood-brain barrier endothelial cells and that Mrp1 and the mdr1b P-gp isoform may be present in other cerebral cells.