20 research outputs found
First molecular analysis of rabies virus in Qatar and clinical cases imported into Qatar, a case report
Identifying the origin of the rabies virus (RABV) infection may have significant implications for control measures. Here, we identified the source of a RABV infection of two Nepalese migrants in Qatar by comparing their RABV genomes with RABV genomes isolated from the brains of a RABV infected camel and fox from Qatar
Rabies Virus Populations in Humans and Mice Show Minor Inter-Host Variability within Various Central Nervous System Regions and Peripheral Tissues
Rabies virus (RABV) has a broad host range and infects multiple cell types throughout the infection cycle. Next-generation sequencing (NGS) and minor variant analysis are powerful tools for studying virus populations within specific hosts and tissues, leading to novel insights into the mechanisms of host-switching and key factors for infecting specific cell types. In this study we investigated RABV populations and minor variants in both original (non-passaged) samples and in vitro-passaged isolates of various CNS regions (hippocampus, medulla oblongata and spinal cord) of a fatal human rabies case, and of multiple CNS and non-CNS tissues of experimentally infected mice. No differences in virus populations were detected between the human CNS regions, and only one non-synonymous single nucleotide polymorphism (SNP) was detected in the fifth in vitro passage of virus isolated from the spinal cord. However, the appearance of this SNP shows the importance of sequencing newly passaged virus stocks before further use. Similarly, we did not detect apparent differences in virus populations isolated from different CNS and non-CNS tissues of experimentally infected mice. Sequencing of viruses obtained from pharyngeal swab and salivary gland proved difficult, and we propose methods for improving sampling
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The inhibitory effect of natural microflora of food on growth of Listeria monocytogenes in enrichment broths
The aims of this study were to (i) compare the inhibitory effects of the natural microflora of different foods on
the growth of Listeria monocytogenes during enrichment in selective and non-selective broths; (ii) to isolate
and identify components of the microflora of the most inhibitory food; and (iii) to determine which of these
components was most inhibitory to growth of L. monocytogenes in co-culture studies. Growth of an antibioticresistant marker strain of L. monocytogenes was examined during enrichment of a range of different foods in
Tryptone Soya Broth (TSB), Half Fraser Broth (HFB) and Oxoid Novel Enrichment (ONE) Broth. Inhibition of
L. monocytogenes was greatest in the presence of minced beef, salami and soft cheese and least with prepared
fresh salad and chicken pâté. For any particular food the numbers of L. monocytogenes present after 24 h
enrichment in different broths increased in the order: TSB, HFB and ONE Broth. Numbers of L. monocytogenes
recovered after enrichment in TSB were inversely related to the initial aerobic plate count (APC) in the food
but with only a moderate coefficient of determination (R2) of 0.51 implying that microbial numbers and the
composition of the microflora both influenced the degree of inhibition of L. monocytogenes. In HFB and ONE
Broth the relationship between APC and final L. monocytogenes counts was weaker. The microflora of TSB after
24 h enrichment of minced beef consisted of lactic acid bacteria, Brochothrix thermosphacta, Pseudomonas spp.,
Enterobacteriaceae, and enterococci. In co-culture studies of L. monocytogenes with different components of the
microflora in TSB, the lactic acid bacteria were the most inhibitory followed by the Enterobacteriaceae. The
least inhibitory organisms were Pseudomonas sp., enterococci and B. thermosphacta. In HFB and ONE Broth the
growth of Gram-negative organisms was inhibited but lactic acid bacteria still reached high numbers after
24 h. A more detailed study of the growth of low numbers of L. monocytogenes during enrichment of minced
beef in TSB revealed that growth of L. monocytogenes ceased at a cell concentration of about 102 cfu/ml when
lactic acid bacteria entered stationary phase. However in ONE Broth growth of lactic acid bacteria was slower
than in TSB with a longer lag time allowing L. monocytogenes to achieve much higher numbers before lactic
acid bacteria reached stationary phase. This work has identified the relative inhibitory effects of different
components of a natural food microflora and shown that the ability of low numbers of L. monocytogenes to
achieve high cell concentrations is highly dependent on the extent to which enrichment media are able to
inhibit or delay growth of the more effective competitors
<i>Kondoa qatarensis </i>f.a., sp. nov., a novel yeast species isolated from marine water in Qatar
<i>Kondoa qatarensis </i>f.a., sp. nov., a novel yeast species isolated from marine water in Qatar
Kondoa qatarensis f.a., sp. nov., a novel yeast species isolated from marine water in Qatar
During a study of yeast diversity in marine waters of the Arabian Gulf surrounding Qatar, 30 strains were isolated that represent a novel species of Kondoa. The isolates were obtained from five locations along the Qatari coast. Species identifications were based on sequence analysis of the internal transcribed spacer (ITS) regions and D1/D2 domains of the large subunit (LSU) rRNA gene. Five strains were selected for further study. The novel species was closely related to Kondoa aeria (CBS 8352T) and Kondoa malvinella (CBS 6082T) but differed from the two species by 5.6 % sequence divergence (16 substitutions and 14 gaps) in the ITS region. On the basis of D1/D2 domains of the LSU rRNA gene, the novel species differed from K. aeria by only >0.35 % sequence divergence (2 substitutions and 0 gaps) and 1.5 % sequence divergence (9 substitutions and 1 gap) to that of K. malvinella. Although the novel species showed a close similarity in the D1/D2 domains to K. aeria (CBS 8352T), based on the significant differences (16 substitutions) in ITS regions and on the basis of physiological and biochemical tests, viz ability to grow at 35 °C, and inability to assimilate, sucrose, raffinose, d,l-lactate, succinate, citrate and nitrite, these strains are considered as novel species of Kondoa. The species name of Kondoa qatarensis f.a., sp. nov. is proposed with specimen 2Y109 as the holotype
<em>Naganishia qatarensis</em> sp. nov., a novel basidiomycetous yeast species from a hypersaline marine environment in Qatar
Fungal diversity of the hypersaline Inland Sea in Qatar
The hypersaline Inland Sea in Qatar constitutes a unique ecosystem characterized by salinities up to saturation, extreme temperature fluctuations, and limited rainfall. To reveal the fungal diversity of this environment, we isolated fungi from water samples collected at the Inland Sea. Taxonomic identification of the isolates was done via DNA barcoding of the ITS1 and ITS2 ribosomal DNA (rDNA) domains and the D1/D2 domains of the nuclear large subunit rDNA. Additional genes, including glyceraldehyde-3-phosphate dehydrogenase (gapdh) and translation elongation factor 1-alpha (tef1), were included for isolates of Alternaria, actin (Act) for Cladosporium, part of the beta-tubulin (BenA) and calmodulin (CaM) genes for Aspergillus and Penicillium. In total, 159 fungal isolates, including 85 Ascomycota and 74 Basidiomycota, were obtained from the water samples collected during four samplings in the winter and summer seasons. About 14% (22/159) of the strains, presumably novel species, were preliminarily identified to the genus level. This is the first report highlighting the diversity of fungi from the hypersaline Inland Sea in Qatar