Home About us Contact
|
Home About us Contact | ||
|
|
||
Distinct Members (distinct + member)
Selected AbstractsHydrolytic enzymes as virulence factors of Candida albicansMYCOSES, Issue 6 2005Martin Schaller Summary Candida albicans is a facultative pathogenic micro-organism that has developed several virulence traits enabling invasion of host tissues and avoidance of host defence mechanisms. Virulence factors that contribute to this process are the hydrolytic enzymes. Most of them are extracellularly secreted by the fungus. The most discussed hydrolytic enzymes produced by C. albicans are secreted aspartic proteinases (Saps). The role of these Saps for C. albicans infections was carefully evaluated in numerous studies, whereas only little is known about the physiological role of the secreted phospholipases (PL) and almost nothing about the involvement of lipases (Lip) in virulence. They may play an important role in the pathogenicity of candidosis and their hydrolytic activity probably has a number of possible functions in addition to the simple role of digesting molecules for nutrition. Saps as the best-studied member of this group of hydrolytic enzymes contribute to host tissue invasion by digesting or destroying cell membranes and by degrading host surface molecules. There is also some evidence that hydrolytic enzymes are able to attack cells and molecules of the host immune system to avoid or resist antimicrobial activity. High hydrolytic activity with broad substrate specificity has been found in several Candida species, most notably in C. albicans. This activity is attributed to multigene families with at least 10 members for Saps and Lips and several members for PL B. Distinct members of these gene families are differentially regulated in various Candida infections. In future, prevention and control of Candida infections might be achieved by pharmacological or immunological tools specifically modulated to inhibit virulence factors, e.g. the family of Saps. [source] A Sarcocystid Misidentified as Hepatozoon didelphydis: Molecular Data from a Parasitic Infection in the Blood of the Southern Mouse Opossum (Thylamys elegans) from ChileTHE JOURNAL OF EUKARYOTIC MICROBIOLOGY, Issue 6 2008SANTIAGO MERINO ABSTRACT. The blood of 21 adult South American mouse opossums (Thylamys elegans) captured from April through August of 2005 in central Chile was examined for parasites. Light microscopic analysis of blood smears initially suggested that a highly pleomorphic Hepatozoon species typical of American opossums was infecting erythrocytes. Unexpectedly, amplification by PCR and sequencing of a DNA fragment of the small subunit rDNA combined with phylogenetic analyses indicated that the parasite is not a member of the suborder Adeleorina, which includes the Haemogregarina and Hepatozoon species, but that it is a clearly distinct member of the suborder Eimeriorina, which includes the cyst-forming family Sarcocystidae. Therefore, a reclassification of this unusual intraerythrocytic apicomplexan will require additional life cycle, microscopic, and molecular analyses. [source] New ways to break an old bond: the bacterial carbon,phosphorus hydrolases and their role in biogeochemical phosphorus cyclingENVIRONMENTAL MICROBIOLOGY, Issue 10 2007John P. Quinn Summary Phosphonates are organophosphorus molecules that contain the highly stable C,P bond, rather than the more common, and more labile, C,O,P phosphate ester bond. They have ancient origins but their biosynthesis is widespread among more primitive organisms and their importance in the contemporary biosphere is increasingly recognized; for example phosphonate-P is believed to play a particularly significant role in the productivity of the oceans. The microbial degradation of phosphonates was originally thought to occur only under conditions of phosphate limitation, mediated exclusively by the poorly characterized C,P lyase multienzyme system, under Pho regulon control. However, more recent studies have demonstrated the Pho-independent mineralization by environmental bacteria of three of the most widely distributed biogenic phosphonates: 2-aminoethylphosphonic acid (ciliatine), phosphonoacetic acid, and 2-amino-3-phosphonopropionic acid (phosphonoalanine). The three phosphonohydrolases responsible have unique specificities and are members of separate enzyme superfamilies; their expression is regulated by distinct members of the LysR family of bacterial transcriptional regulators, for each of which the phosphonate substrate of the respective degradative operon serves as coinducer. Previously no organophosphorus compound was known to induce the enzymes required for its own degradation. Whole-genome and metagenome sequence analysis indicates that the genes encoding these newly described C,P hydrolases are distributed widely among prokaryotes. As they are able to function under conditions in which C,P lyases are inactive, the three enzymes may play a hitherto-unrecognized role in phosphonate breakdown in the environment and hence make a significant contribution to global biogeochemical P-cycling. [source] The North American cranberry fruit rot fungal community: a systematic overview using morphological and phylogenetic affinitiesPLANT PATHOLOGY, Issue 6 2009J. J. Polashock Cranberry fruit rot (CFR) is caused by many species of fungi, with the contribution of any given species to the disease complex varying among plantings of Vaccinium macrocarpon within a site, sites within regions, and among regions and years. This study assessed the morphological and molecular variability of five widespread CFR-causing fungi: Phyllosticta vaccinii, Coleophoma empetri, Colletotrichum acutatum, Colletotrichum gloeosporioides and Physalospora vaccinii. Although the majority of isolates had morphological characteristics consistent with published descriptions, some were atypical. For example, non-chromogenic isolates of C. acutatum were recovered from British Columbia and white isolates of Physalospora vaccinii were recovered in addition to the more common dark isolates. On the basis of sequence analysis of the ITS and large subunit rDNA (LSU), it appears that Phyllosticta vaccinii, C. empetri, C. gloeosporioides and C. acutatum are genetically uniform on cranberry in North America. This suggests the possibility that these fungal species were introduced to cultivated cranberries and concomitantly moved with planting material to new locations. In contrast, white isolates of Physalospora had ITS and LSU sequences distinct from those of their dark counterparts, with phylogenetic analyses suggesting that these isolates represent either different species or distinct members of highly divergent populations. Taxonomic placement of all species based on phylogenetic relationships was consistent with morphological placement, with the exception of Physalospora vaccinii. Unlike other Physalospora species, CFR isolates of Physalospora vaccinii were not allied with the Xylariomycetidae; instead, these fungi were members of the Sordariomycetidae. A deeper taxonomic analysis is needed to resolve this inconsistency in familial affiliation. [source] Prunus necrotic ringspot virus isolates in stone fruit germplasm accessions and cultivars in IsraelANNALS OF APPLIED BIOLOGY, Issue 2 2004S SPIEGEL Summary Prunus necrotic ringspot virus (PNRSV) was detected in almonds, plum and apricot germplasm accessions and local almond cultivars in Israel. PNRSV was widespread both in wild and cultivated almond trees and uncommon in wild apricots and plums. The possible variation among the PNRSV isolates was initially evaluated by restriction analysis of PCR products representing the CP gene with the endonuclease RsaI and followed by nucleotide sequence analysis of selected isolates. It was concluded that all 13 isolates belong to group PV96, the largest cluster of PNRSV isolates, described previously. Two PNRSV isolates, one from a plum accession and one from an almond cultivar, were found to be distinct members of group PV96 with unique nucleotide modifications not found in other documented isolates of this virus. However, no PNRSV isolate typical to a specific host and/or to the Middle East region could be identified. This study expands the body of data on variability of PNRSV isolates and highlights the importance of assessing the virus status of germplasm collections by applying reliable diagnostic and differentiating methods. [source] | ||||||||||