Biology subjects

Abdullah, F.

Publications and source records attributed to Abdullah, F..

2 recordsLinked to original sources

bioRxiv2026

Maxillary constriction causes nasal septum deviation and deformity of the nasal floor

IntroductionWe investigated the direct effect of transverse maxillary constriction on nasal septal deviation (NSD) and nasal floor slanting. Methods and Materials60 growing Wistar rats (21days old) were divided into four groups (n=15): 1) Experimental Group 1 received active constriction force (100cN), 2) Experimental Group 2 received active expansion force (100cN), 3) Sham received the same spring as Experimental Groups without receiving any active force, and 4) Control group did not receive any appliance. Samples were collected after 28 days for microcomputed tomography (CT) analysis. ResultsExperimental Group 1 demonstrated maxillary constriction (both skeletal and dental), accompanied by mandibular shift on closure, clockwise mandibular rotation, and increased mandibular plane angle and facial height. Constriction also produced severe nasal floor slanting in the molar area that extended posteriorly. Nasal floor canting was accompanied by a slanted vomer and a C-shaped NSD. The direction of nasal floor canting and mandibular shift was always similar. Experimental Group 2, on the other hand, was not associated with nasal deviation, and a slight slanting of the nasal floor was observed only when there was a mandibular shift. ConclusionOur study suggests that the constricting transverse forces applied to the maxilla can induce slanting of the nasal floor and, consequently, the vomer, which in turn can lead to nasal septal deviation. Slanting of the nasal floor is caused mainly by rotation of the hemimaxilla in response to transverse forces and changes in occlusal forces due to a mandibular shift.

developmental biology↗

bioRxiv2019

Immunoinformatic and dynamic simulation-based designing of a multi-epitope vaccine against emerging pathogen Elizabethkingia anophelis

Elizabethkingia anophelis is an emerging human pathogen causing neonatal meningitis, catheter-associated infections and nosocomial outbreaks with high mortality rates. Besides, they are resistant to most antibiotics used in empirical therapy. In this study, therefore, we used immunoinformatic approaches to design an epitope-based vaccine against E. anophelis as an alternative preventive measure. Initially, T-cell (CTL and HTL) and B-cell (LBL) epitopes were predicted from the highest antigenic protein. The CTL and HTL epitopes together had a population coverage of 99.97% around the world. Eventually, 6 CTL, 7 HTL, and 2 LBL epitopes were selected and used to construct a multiepitope vaccine. The vaccine protein was found to be highly immunogenic, non-allergenic, and non-toxic. Codon adaptation and in silico cloning were performed to ensure better expression within E. coli K12 host system. The stability of the vaccine structure was also improved by disulphide bridging. In addition, molecular docking and dynamic simulation revealed good and stable binding affinity between the vaccine and receptor. The immune simulation showed higher levels of T-cell and B-cell activities which was in coherence with actual immune response. Repeated exposure simulation resulted in higher clonal selection and faster antigen clearance. Nevertheless, experimental validation is required to ensure the immunogenic potency and safety of this vaccine to control E. anophelis infection in the future.

bioinformatics↗