48 research outputs found

    Compensatory and susceptive responses of cowpea genotypes to infestation by aphis Craccivora koch.

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    The aim of the study was to estimate yield loss to10 selected genotypes of cowpea as a result of Aphis craccivora infestation during the vegetative phase of the crop. There were two trials with four replications. The first trial serving as the control was sprayed at the seedling, flowering andpodding stages against insect pests with lambda cyhalothrin (PAWA®). The other trial was sprayed only at flowering and podding stages. The cowpea seedlings of the second trial were infested with five four-day-old aphids per seedling two weeks after planting. The aphids were allowed to form colonies and fed on the seedlings until symptoms of damage were observed. When the susceptible seedlings became stunted with distorted leaves and yellowing of leaves at two weeks after infestation (28 days after planting), aphids were controlled. The results showed that aphids’ infestation delayed flowering and maturity of genotypes of cowpea. With the exception of early flowering genotypes all the medium to late flowering genotypes produced higher dry grain yield in infested plots than the control plots. The trend was not different from the production of dry biomass. The results of the present study implies that control of aphids infestation inearly maturing cowpea genotypes should not be delayed up to two weeks after infestation or 28 days after planting. Aphid’s infestation period for studies in susceptive response in medium to late maturing genotypes should go beyond 28 days after planting probably up to 35 days afterplanting

    Allergic Rhinitis and its Associated Co-Morbidities at Bugando Medical Centre in Northwestern Tanzania; A Prospective Review of 190 Cases.

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    Allergic rhinitis is one of the commonest atopic diseases which contribute to significant morbidity world wide while its epidemiology in Tanzania remains sparse. There was paucity of information regarding allergic rhinitis in our setting; therefore it was important to conduct this study to describe our experience on allergic rhinitis, associated co-morbidities and treatment outcome in patients attending Bugando Medical Centre. This was descriptive cross-sectional study involving all patients with a clinical diagnosis of allergic rhinitis at Bugando Medical Centre over a three-month period between June 2011 and August 2011. Data was collected using a pre-tested coded questionnaire and analyzed using SPSS statistical computer software version 17.0. A total of 190 patients were studied giving the prevalence of allergic rhinitis 14.7%. The median age of the patients was 8.5 years. The male to female ratio was 1:1. Adenoid hypertrophy, tonsillitis, hypertrophy of inferior turbinate, nasal polyps, otitis media and sinusitis were the most common co-morbidities affecting 92.6% of cases and were the major reason for attending hospital services. Sleep disturbance was common in children with adenoids hypertrophy (χ2 = 28.691, P = 0.000). Allergic conjunctivitis was found in 51.9%. The most common identified triggers were dust, strong perfume odors and cold weather (P < 0.05). Strong perfume odors affect female than males (χ2 = 4.583, P = 0.032). In this study family history of allergic rhinitis was not a significant risk factor (P =0.423). The majority of patients (68.8%) were treated surgically for allergic rhinitis co morbidities. Post operative complication and mortality rates were 2.9% and 1.6% respectively. The overall median duration of hospital stay of in-patients was 3 days (2 - 28 days). Most patients (98.4%) had satisfactory results at discharge. The study shows that allergic rhinitis is common in our settings representing 14.7% of all otorhinolaryngology and commonly affecting children and adolescent. Sufferers seek medical services due to co-morbidities of which combination of surgical and medical treatment was needed. High index of suspicions in diagnosing allergic rhinitis and early treatment is recommended

    The Ubiquitin/Proteasome System Mediates Entry and Endosomal Trafficking of Kaposi's Sarcoma-Associated Herpesvirus in Endothelial Cells

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    Ubiquitination, a post-translational modification, mediates diverse cellular functions including endocytic transport of molecules. Kaposi's sarcoma-associated herpesvirus (KSHV), an enveloped herpesvirus, enters endothelial cells primarily through clathrin-mediated endocytosis. Whether ubiquitination and proteasome activity regulates KSHV entry and endocytosis remains unknown. We showed that inhibition of proteasome activity reduced KSHV entry into endothelial cells and intracellular trafficking to nuclei, thus preventing KSHV infection of the cells. Three-dimensional (3-D) analyses revealed accumulation of KSHV particles in a cytoplasmic compartment identified as EEA1+ endosomal vesicles upon proteasome inhibition. KSHV particles are colocalized with ubiquitin-binding proteins epsin and eps15. Furthermore, ubiquitination mediates internalization of both KSHV and one of its receptors integrin β1. KSHV particles are colocalized with activated forms of the E3 ligase c-Cbl. Knock-down of c-Cbl or inhibition of its phosphorylation reduced viral entry and intracellular trafficking, resulting in decreased KSHV infectivity. These results demonstrate that ubiquitination mediates internalization of both KSHV and one of its cognate receptors integrin β1, and identify c-Cbl as a potential E3 ligase that facilitates this process

    New Sources of Resistance in Cowpea to the Cowpea Aphid (Aphis Craccivora Koch) (Homoptera: Aphididae)

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    Twenty-two advanced breeding genotypes of cowpea were evaluated for their responses to infes-tation by the cowpea aphid, Aphis craccivora Koch. The aim of the study was to identify geno-type(s) of cowpea resistant to A. craccivora to be used as breeding line(s). Seedling screening technique and aphid growth and reproduction on each genotype were used to classify the geno-types into resistant and susceptible groups. The cowpea genotypes SARC 1-57-2 and SARC 1-91-1 were found to be the most resistant genotypes, whereas five of the genotypes namely, Apag-baala, IT 97K-499-35, IT 98K-506-1, IT 95K-193-2 and Marfo-Tuya were highly susceptible. The high susceptibility of the IITA lines must be a cause for concern, particularly the IT 97K-499-35 line which is known to be resistant to A. craccivora in Nigeria. This suggests the exis-tence of cowpea aphid biotype in northern Ghana which is more virulent than the biotypes in Nigeria. The results support earlier findings of the development of aphid biotypes that are more aggressive and are not controlled by the aphid resistance varieties of cowpea developed by IITA for Nigeria

    Malaria-induced interferon-γ drives the expansion of Tbethi atypical memory B cells

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    Many chronic infections, including malaria and HIV, are associated with a large expansion of CD21-CD27- 'atypical' memory B cells (MBCs) that exhibit reduced B cell receptor (BCR) signaling and effector functions. Little is known about the conditions or transcriptional regulators driving atypical MBC differentiation. Here we show that atypical MBCs in malaria-exposed individuals highly express the transcription factor T-bet, and that T-bet expression correlates inversely with BCR signaling and skews toward IgG3 class switching. Moreover, a longitudinal analysis of a subset of children suggested a correlation between the incidence of febrile malaria and the expansion of T-bethi B cells. The Th1-cytokine containing supernatants of malaria-stimulated PBMCs plus BCR cross linking induced T-bet expression in naïve B cells that was abrogated by neutralizing IFN-γ or blocking the IFN-γ receptor on B cells. Accordingly, recombinant IFN-γ plus BCR cross-linking drove T-bet expression in peripheral and tonsillar B cells. Consistent with this, Th1-polarized Tfh (Tfh-1) cells more efficiently induced T-bet expression in naïve B cells. These data provide new insight into the mechanisms underlying atypical MBC differentiation
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