Emmanuel Nnadi

Mr. Emmanuel Nnadi


Research Focus & Metrics

Academic Career Length

15Years (2012-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 October 2012 in Medical Mycology
Verified
Journal Article
Open access
PDF file
ENEmmanuel Nnadi
Emmanuel Nnadi
GAGrace Mebi Ayanbimpe
Grace Mebi Ayanbimpe
FSFabio Scordino
Fabio Scordino
MOMark Ojogba Okolo
Mark Ojogba Okolo
IEIfeoma Bessy Enweani
Ifeoma Bessy Enweani
OROrazio Romeo
Orazio Romeo
During a survey of the prevalence of Candida spp. in Jos, Plateau State, Nigeria, two atypical C. albicans isolates were recovered. These two yeasts

1 December 2016 in Journal of Medical Mycology
Verified
Journal Article
Closed access
ENEmmanuel Nnadi
Emmanuel Nnadi
IEIfeoma Enweani
Ifeoma Enweani
MCMassimo Cogliati
Massimo Cogliati
GAG.M. Ayanbimpe
G.M. Ayanbimpe
MOM.O. Okolo
M.O. Okolo
FSF. Scordino
F. Scordino

1 April 2020 in bioRxiv
Verified
Preprint
Open access
PDF file
AUAmaka Ubani
Amaka Ubani
FAFrancis Agwom
Francis Agwom
OROluwatoyin RuthMorenikeji
Oluwatoyin RuthMorenikeji
SNShehu Nathan
Shehu Nathan
PLPam Dachung LUKA
Pam Dachung LUKA
JAJohn Chinyere Aguiyi
John Chinyere Aguiyi
COV spike (S) glycoprotein and M pro are two key targets that have been identified for vaccines and drug development against the COVID-19 disease. Virtual screening of some compounds of plants origin that have shown antiviral activities were carried out on the two targets, 6lu7 and 6vsb by docking with the PyRx software. The binding affinities were compared with other compounds and drugs already identified as potential ligands for 6lu7 and 6vsb as well as Chloroquine and hydroxychloroquine. The docked compounds with best binding affinities were also filtered for drug likeness using the SwissADME and PROTOX platforms on the basis of Physicochemical properties and toxicity respectively. The docking results revealed that scopodulcic acid and dammarenolic acid had the best binding affinity on the s-glycoprotein and M pro protein targets respectively. Silybinin also demonstrated a good binding affinity to both protein targets making it a potential candidate for further evaluation as repurposed candidate for SARS COV2 with likelihood of having a multitarget activity.

21 September 2020 in F1000Research
Verified
Journal Article
Open access
PDF file
AUAmaka Ubani
Amaka Ubani
FAFrancis Agwom
Francis Agwom
OMOluwatoyin Ruth Morenikeji
Oluwatoyin Ruth Morenikeji
NSNathan Yakubu Shehu
Nathan Yakubu Shehu
EUEmmanuel Arinze Umera
Emmanuel Arinze Umera
PLPam Dachung Luka
Pam Dachung Luka
Background: The coronavirus spike (S) glycoprotein and M protease are two key targets that have been identified for vaccines and drug development against COVID-19. Methods: Virtual screening of some compounds of plant origin that have shown antiviral activities were carried out on the two targets, the M protease (PDB ID 6LU7) and S glycoprotein (PDB ID 6VSB), by docking with PyRx software. The binding affinities were compared with other compounds and drugs already identified as potential ligands for the M protease and S glycoprotein, as well as chloroquine and hydroxychloroquine. The docked compounds with best binding affinities were also filtered for drug likeness using the SwissADME and PROTOX platforms on the basis of physicochemical properties and toxicity, respectively. Results: The docking results revealed that scopadulcic acid and dammarenolic acid had the best binding affinity for the S glycoprotein and Mpro protein targets, respectively. Silybinin, through molecular docking, also demonstrated good binding affinity for both protein targets making it a potential candidate for further evaluation as repurposed candidate for SARS-CoV-2, with likelihood of having multitarget activity as it showed activities for both targets. Conclusions: The study proposes that scopadulcic acid and dammarenolic acid be further evaluated in vivo for drug formulation against SARS-COV-2 and possible repurposing of Silybinin for the management of COVIV-19.

26 July 2024 in Microorganisms
Verified
Journal Article
Open access
PDF file
NSNancy Milton Sati
Nancy Milton Sati
RCRoderick Card
Roderick Card
LBLisa Barco
Lisa Barco
MMMaryam Muhammad
Maryam Muhammad
PLPam Dachung LUKA
Pam Dachung LUKA
FMFrank N. Mwiine
Frank N. Mwiine
There is scant information on Salmonella in indigenous poultry in Nigeria. We investigated the occurrence and characterized Salmonella serovars in indigenous poultry and their drinking water sources to enhance the monitoring of the infection in poultry and to promote public health. We collected 1208 samples, poultry droppings (n = 1108), and water (n = 100) across 15 markets in North Central Nigeria. Salmonella spp. were isolated following World Organisation for Animal Health guidelines. Salmonella spp., confirmed through invA gene detection by a polymerase chain reaction assay, were 6.8% (75/1108) droppings and 3% (3/100) water. Susceptibility testing against 13 antimicrobials showed 60.3% (47/78) susceptibility to all the antimicrobials tested while 14.1% (11/78) were multidrug resistant. Serotyping and whole-genome sequencing were carried out on 44 of the isolates, and 23 different serovars were identified. Genomes of serovars Luedinghausen, Laredo, Widemarsh, and Lansing are being documented in Africa for the first time. Twenty (20) antimicrobial resistance (AMR) gene markers encoding for resistance to aminoglycosides, tetracyclines, sulphonamides, quinolones, trimethoprim, penicillins and phenicols were found. Phylogenetic cluster analysis showed close relatedness among isolates from different sources. This study shows both low Salmonella prevalence and AMR, but since uncommon serovars are circulating, continuous monitoring is recommended so as to ensure food safety and poultry health.

5 March 2016 in European Journal of Clinical Microbiology & Infectious Diseases
Verified
Journal Article
Closed access
PDF file
VCV. Chillemi
V. Chillemi
CPC. Lo Passo
C. Lo Passo
ADA. D. van Diepeningen
A. D. van Diepeningen
SRS. Rharmitt
S. Rharmitt
DDD. Delfino
D. Delfino
FSF. Scordino
F. Scordino