Pius Ekong

Dr. Pius Ekong


Research Focus & Metrics

Academic Career Length

17Years (2010-Present)

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

Representative Publications

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1 September 2015 in Preventive Veterinary Medicine
Verified
Journal Article
Closed access
PEPius Ekong
Pius Ekong
MSMichael W. Sanderson
Michael W. Sanderson
NCNatalia Cernicchiaro
Natalia Cernicchiaro

6 January 2010 in Virus Genes
Verified
Journal Article
Closed access
PDF file
OOOlajide A. Owolodun
Olajide A. Owolodun
Armanda BastosArmanda Bastos
Armanda Bastos
JAJohn F. Antiabong
John F. Antiabong
MOMosunmola E. Ogedengbe
Mosunmola E. Ogedengbe
PEPius Ekong
Pius Ekong
BYBitrus Yakubu
Bitrus Yakubu

1 February 2012 in Preventive Veterinary Medicine
Verified
Journal Article
Closed access
PEPius Ekong
Pius Ekong
EDEls Ducheyne
Els Ducheyne
TCTim E. Carpenter
Tim E. Carpenter
OOOlajide A. Owolodun
Olajide A. Owolodun
AOAgnes T. Oladokun
Agnes T. Oladokun
DBDirk Berkvens
Dirk Berkvens

30 December 2014 in Tropical Animal Health and Production
Verified
Journal Article
Closed access
PDF file
TWTimothy Yusufu Woma
Timothy Yusufu Woma
DKDemo Joab Usman Kalla
Demo Joab Usman Kalla
PEPius Ekong
Pius Ekong
HUHussaini Gulak Ularamu
Hussaini Gulak Ularamu
SCSolomon Chuwang Chollom
Solomon Chuwang Chollom
Melvyn QuanMelvyn Quan
Melvyn Quan

9 March 2016 in Onderstepoort Journal of Veterinary Research
Verified
Journal Article
Open access
TWTimothy Y. Woma
Timothy Y. Woma
PEPius Ekong
Pius Ekong
DBDauda G. Bwala
Dauda G. Bwala
JIJohn O. Ibu
John O. Ibu
LTLouisa Ta’aMa
Louisa Ta’aMa
Melvyn QuanMelvyn Quan
Melvyn Quan
Peste des petits ruminants, caused by the peste des petits ruminants virus (PPRV), is a highly contagious and economically important transboundary viral disease of domestic and wild small ruminants and a major hindrance to small-ruminant production in Nigeria. The seroprevalence and distribution of PPRV antibodies in small ruminants in rural households, farms, live animal markets and slaughter slabs across the six different agro-ecological zones of Nigeria were determined. A total of 4548 serum samples from 3489 goats and 1059 sheep were collected in 12 states. A PPRV competitive enzyme-linked immunosorbent assay was used to test the samples and the data analysed with R statistical software version 3.0.1. The study animals included all ages and both sexes. The overall prevalence estimate of sera positive for PPRV antibodies was 23.16% (n = 1018 positive samples per 4548 total samples, 95% confidence interval: 21.79% – 24.57%). There were significant differences in the seroprevalence between the states (p = 0.001). Taraba State had the highest seroprevalence of 29.51%, whilst the lowest seroprevalence of 14.52% was observed in Cross River State. There were no significant differences in the PPRV seroprevalence between male and female animals (p = 0.571), age (p = 0.323) and between species (p = 0.639). These data indicate the current seroprevalence to PPRV in the small-ruminant population in Nigeria.

20 April 2021 in PeerJ
Verified
Journal Article
Open access
PDF file
Essam AbdelfattahEssam Abdelfattah
Essam Abdelfattah
PEPius Ekong
Pius Ekong
EOEmmanuel Okello
Emmanuel Okello
TCTapakorn Chamchoy
Tapakorn Chamchoy
BKBetsy Karle
Betsy Karle
Sharif S. AlySharif S. Aly
Sharif S. Aly
Background: This study describes the occurrence of antimicrobial resistance (AMR) in commensal Escherichia coli and Enterococcus/Streptococcus spp. (ES) isolated from fecal samples of dairy cows and assesses the variation of AMR profiles across regions and seasons following the implementation of the Food and Agricultural Code (FAC) Sections 14400–14408 (formerly known as Senate Bill, SB 27) in California (CA). Methods: The study was conducted on ten dairies distributed across CA’s three milk sheds: Northern California (NCA), Northern San Joaquin Valley (NSJV), and the Greater Southern California (GSCA). On each study dairy, individual fecal samples were collected from two cohorts of lactating dairy cows during the fall/winter 2018 and spring/summer 2019 seasons. Each cohort comprised of 12 cows per dairy. The fecal samples were collected at enrollment before calving (close-up stage) and then monthly thereafter for four consecutive time points up to 120 days in milk. A total of 2,171 E. coli and 2,158 ES isolates were tested for antimicrobial susceptibility using the broth microdilution method against a select panel of antimicrobials. Results: The E. coli isolates showed high resistance to florfenicol (83.31% ± 0.80) and sulphadimethoxine (32.45%), while resistance to ampicillin (1.10% ± 0.21), ceftiofur (1.93% ± 0.29), danofloxacin (4.01% ± 0.42), enrofloxacin (3.31% ± 0.38), gentamicin (0.32% ± 0.12) and neomycin (1.61% ± 0.27) had low resistance proportions. The ES isolates were highly resistant to tildipirosin (50.18% ± 1.10), tilmicosin (48% ± 1.10), tiamulin (42%) and florfenicol (46% ± 1.10), but were minimally resistant to ampicillin (0.23%) and penicillin (0.20%). Multidrug resistance (MDR) (resistance to at least 1 drug in ≥3 antimicrobial classes) was observed in 14.14% of E. coli isolates and 39% of ES isolates. Escherichia coli isolates recovered during winter showed higher MDR prevalence compared to summer isolates (20.33% vs. 8.04%). A higher prevalence of MDR was observed in NSJV (17.29%) and GSCA (15.34%) compared with NCA (10.10%). Conclusions: Our findings showed high rates of AMR to several drugs that are not labeled for use in lactating dairy cattle 20 months of age or older. Conversely, very low resistance was observed for drugs labeled for use in adult dairy cows, such as cephalosporins and penicillin. Overall, our findings identified important differences in AMR by antimicrobial class, region and season.