Development of Electrochemical DNA Biosensor for Equine Hindgut Acidosis Detection

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Development of Electrochemical DNA Biosensor for Equine Hindgut Acidosis Detection. / Davies, Joshua; Thomas, Carol; Mohammad, Rizwan et al.
Yn: Sensors, Cyfrol 21, Rhif 7, 01.04.2021.

Allbwn ymchwil: Cyfraniad at gyfnodolynErthygladolygiad gan gymheiriaid

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Davies J, Thomas C, Mohammad R, Gwenin C. Development of Electrochemical DNA Biosensor for Equine Hindgut Acidosis Detection. Sensors. 2021 Ebr 1;21(7). Epub 2021 Maw 26. doi: 10.3390/s21072319

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Davies, Joshua ; Thomas, Carol ; Mohammad, Rizwan et al. / Development of Electrochemical DNA Biosensor for Equine Hindgut Acidosis Detection. Yn: Sensors. 2021 ; Cyfrol 21, Rhif 7.

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TY - JOUR

T1 - Development of Electrochemical DNA Biosensor for Equine Hindgut Acidosis Detection

AU - Davies, Joshua

AU - Thomas, Carol

AU - Mohammad, Rizwan

AU - Gwenin, Christopher

PY - 2021/4/1

Y1 - 2021/4/1

N2 - The pH drop in the hindgut of the horse is caused by lactic acid-producing bacteria which are abundant when a horse's feeding regime is excessively carbohydrate rich. This drop in pH below six causes hindgut acidosis and may lead to laminitis. Lactic acid-producing bacteria and have been found to produce high amounts of L-lactate and D-lactate, respectively. Early detection of increased levels of these bacteria could allow the horse owner to tailor the horse's diet to avoid hindgut acidosis and subsequent laminitis. Therefore, 16s ribosomal ribonucleic acid (rRNA) sequences were identified and modified to obtain target single stranded deoxyribonucleic acid (DNA) from these bacteria. Complementary single stranded DNAs were designed from the modified target sequences to form capture probes. Binding between capture probe and target single stranded deoxyribonucleic acid (ssDNA) in solution has been studied by gel electrophoresis. Among pairs of different capture probes and target single stranded DNA, hybridization of capture probe 1 (SECP1) and target 1 (SET1) was portrayed as gel electrophoresis. Adsorptive stripping voltammetry was utilized to study the binding of thiol modified SECP1 over gold on glass substrates and these studies showed a consistent binding signal of thiol modified SECP1 and their hybridization with SET1 over the gold working electrode. Cyclic voltammetry and electrochemical impedance spectroscopy were employed to examine the binding of thiol modified SECP1 on the gold working electrode and hybridization of thiol modified SECP1 with the target single stranded DNA. Both demonstrated the gold working electrode surface was modified with a capture probe layer and hybridization of the thiol bound ssDNA probe with target DNA was indicated. Therefore, the proposed electrochemical biosensor has the potential to be used for the detection of the non-synthetic bacterial DNA target responsible for equine hindgut acidosis.

AB - The pH drop in the hindgut of the horse is caused by lactic acid-producing bacteria which are abundant when a horse's feeding regime is excessively carbohydrate rich. This drop in pH below six causes hindgut acidosis and may lead to laminitis. Lactic acid-producing bacteria and have been found to produce high amounts of L-lactate and D-lactate, respectively. Early detection of increased levels of these bacteria could allow the horse owner to tailor the horse's diet to avoid hindgut acidosis and subsequent laminitis. Therefore, 16s ribosomal ribonucleic acid (rRNA) sequences were identified and modified to obtain target single stranded deoxyribonucleic acid (DNA) from these bacteria. Complementary single stranded DNAs were designed from the modified target sequences to form capture probes. Binding between capture probe and target single stranded deoxyribonucleic acid (ssDNA) in solution has been studied by gel electrophoresis. Among pairs of different capture probes and target single stranded DNA, hybridization of capture probe 1 (SECP1) and target 1 (SET1) was portrayed as gel electrophoresis. Adsorptive stripping voltammetry was utilized to study the binding of thiol modified SECP1 over gold on glass substrates and these studies showed a consistent binding signal of thiol modified SECP1 and their hybridization with SET1 over the gold working electrode. Cyclic voltammetry and electrochemical impedance spectroscopy were employed to examine the binding of thiol modified SECP1 on the gold working electrode and hybridization of thiol modified SECP1 with the target single stranded DNA. Both demonstrated the gold working electrode surface was modified with a capture probe layer and hybridization of the thiol bound ssDNA probe with target DNA was indicated. Therefore, the proposed electrochemical biosensor has the potential to be used for the detection of the non-synthetic bacterial DNA target responsible for equine hindgut acidosis.

KW - DNA hybridization

KW - Mitsuokella jalaludinii

KW - Streptococcus equinus

KW - electrochemical biosensor

KW - equine hindgut acidosis

KW - laminitis

KW - point-of-care testing

KW - veterinary diagnostics

U2 - 10.3390/s21072319

DO - 10.3390/s21072319

M3 - Article

C2 - 33810389

VL - 21

JO - Sensors

JF - Sensors

SN - 1424-8220

IS - 7

ER -