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Macharia, S.

Publications and source records attributed to Macharia, S..

2 recordsLinked to original sources

Overexpression of MusaVicilin Gene for Disease Resistance in Banana

Banana Xanthomonas wilt (BXW) disease, caused by Xanthomonas vasicola pv. musacearum, is a major constraint to banana production in East and Central Africa. All cultivated banana varieties are susceptible, with the wild progenitor Musa balbisiana being the only known source of complete resistance. Limitations in classical breeding have prompted the exploration of molecular genetic tools, such as genetic modification, to develop resistant cultivars. Comparative transcriptomic analyses revealed a five-fold upregulation of MusaVicilin gene in M. balbisiana (BB genome) compared to the BXW- susceptible Pisang Awak when challenged with the pathogen, suggesting its role in defense. This study investigated whether constitutive overexpression of the MusaVicilin gene cloned from M. balbisiana could enhance resistance to BXW in the susceptible Sukali Ndiizi cultivar (AAB genome). Transgenic events were developed with the MusaVicilin gene under the control of the constitutive CaMV 35S promoter. These events exhibited enhanced disease resistance compared with non-transgenic control plants. The overexpression of MusaVicilin highlights its potential as a candidate gene for engineering resistance to BXW in susceptible cultivars. Moreover, MusaVicilin could serve as a valuable component in gene stacking strategies aimed at developing durable, disease-resistant banana varieties.

synthetic biology↗

Pericardial & Mediastinal Fat-Associated Lymphoid Clusters are rapidly activated in an alkane induced model of Systemic Lupus Erythematosus

Systemic Lupus Erythematosus (SLE) is an autoimmune disease predominated by auto-antibodies that recognise cellular components. Pleural involvement is the most common SLE-related lung disease. Natural antibodies are rapidly secreted by innate-like B cells following perturbation of homeostasis and are important in the early stages of immune activation. The serous cavities are home to large numbers of innate-like B cells present both within serous fluid and resident within fat-associated lymphoid clusters (FALCs). FALCs are important hubs for B-cell activation and local antibody secretion within the body cavities. Patients with SLE can develop anti-phospholipid antibodies and in rare situations develop alveolar haemorrhage. Utilising delivery of the hydrocarbon oil pristane in C57BL/6 mice as a model of SLE we identify a rapid expansion of pleural cavity B cells as early as day 3 after intra-peritoneal pristane delivery. Following pristane delivery, pericardial B1 B cells are proliferative, express the plasma-cell surface marker CD138 and secrete both innate and class switched antibodies highlighting that this cavity niche may play an unrecognised role in the initiation of lupus pleuritis. Graphical abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=163 SRC="FIGDIR/small/549766v1_ufig1.gif" ALT="Figure 1"> View larger version (31K): org.highwire.dtl.DTLVardef@18ea5bforg.highwire.dtl.DTLVardef@23d9deorg.highwire.dtl.DTLVardef@1b48b3aorg.highwire.dtl.DTLVardef@20a133_HPS_FORMAT_FIGEXP M_FIG C_FIG

immunology↗