Suspension array for multiplex immunoassay of five common endocrine disrupter chemicals

2021 ◽  
Vol 188 (9) ◽  
Author(s):  
Xue-xia Jia ◽  
Zi-yi Yao ◽  
Sha Liu ◽  
Zhi-xian Gao
2019 ◽  
Vol 132 ◽  
pp. 47-54 ◽  
Author(s):  
Kexiao Zheng ◽  
Chao Chen ◽  
Xiuli Chen ◽  
Menghong Xu ◽  
Linqi Chen ◽  
...  

2020 ◽  
Vol 19 (1) ◽  
Author(s):  
Diane Wallace Taylor ◽  
Naveen Bobbili ◽  
Alex Kayatani ◽  
Samuel Tassi Yunga ◽  
Winifrida Kidima ◽  
...  

Plant Disease ◽  
2019 ◽  
Vol 103 (6) ◽  
pp. 1213-1219
Author(s):  
Zehua Su ◽  
Xin Zhang ◽  
Jianjiang Zhao ◽  
Wenqiao Wang ◽  
Lei Shang ◽  
...  

To provide a high-throughput, efficient, and accurate method to monitor multiple-fungicide resistance of Botrytis cinerea in the field, we used the suspension array, sequencing, and mycelial growth assay in our research. Discriminating-dose bioassays for detecting carbendazim, diethofencarb, boscalid, and iprodione resistance (CarR, DieR, BosR, and IprR, respectively) were used to analyze 257 isolates collected from Hebei Province in China during 2016 and 2017. High resistance frequencies to carbendazim (100%), diethofencarb (92.08%), and iprodione (86.59%) were detected. BosR isolates accounted for 11.67% of the total. In addition, 103 isolates were randomly selected for phenotype and genotype detection. The high-throughput suspension array was utilized to detect eight genotypes simultaneously, including BenA-E198, BenA-198A, SdhB-H272, SdhB-272Y, BcOS1-I365, BcOS1-365S, erg27-F412, and erg27-412S, which were associated with resistance toward carbendazim or diethofencarb, boscalid, iprodione, and fenhexamid (FenR), respectively. Most of the benzimidazole-resistant isolates (81.55%) possessed the E198V mutation in the BenA gene. Ninety-three isolates with dual resistance to carbendazim and diethofencarb showed the E198V/K mutation. All BosR isolates carried the H272R mutation in the SdhB gene. The I365S and Q369P+N373S (66.99%) mutations in the BcOS1 gene were more frequently observed. No mutation was detected in the erg27 gene in Hebei isolates. There were 13 resistance profile phenotypes. Phenotypes with triple resistance were the most common (83.50%), and CarRDieRBosSIprRFenS was the major type. CarR isolates that carried E198V/K/A were all highly resistant (HR) and only one F200Y mutant was moderately resistant (MR) to carbendazim. Isolates that possessed E198V/K were MR or HR to diethofencarb. BosR isolates that possessed H272R mutation were lowly resistant (LR). IprR isolates were all LR or MR. The distribution of half maximal effective concentrations of CarR isolates with E198V/K mutations and IprR isolates with Q369P+N373S mutations significantly increased from 2016 to 2017. Combined with our observations, a combination method of the high-throughput suspension array and the mycelial growth assay was suggested to accurately monitor multiple resistance of B. cinerea in the field.


2011 ◽  
Vol 10 (1) ◽  
pp. 192 ◽  
Author(s):  
Edmilson Rui ◽  
Carmen Fernandez-Becerra ◽  
Satoru Takeo ◽  
Sergi Sanz ◽  
Marcus VG Lacerda ◽  
...  

2015 ◽  
Vol 2015 ◽  
pp. 1-13 ◽  
Author(s):  
Cécile Beck ◽  
Philippe Desprès ◽  
Sylvie Paulous ◽  
Jessica Vanhomwegen ◽  
Steeve Lowenski ◽  
...  

West Nile virus (WNV), Japanese encephalitis virus (JEV), and tick-borne encephalitis virus (TBEV) are flaviviruses responsible for severe neuroinvasive infections in humans and horses. The confirmation of flavivirus infections is mostly based on rapid serological tests such as enzyme-linked immunosorbent assays (ELISAs). These tests suffer from poor specificity, mainly due to antigenic cross-reactivity among flavivirus members. Robust diagnosis therefore needs to be validated through virus neutralisation tests (VNTs) which are time-consuming and require BSL3 facilities. The flavivirus envelope (E) glycoprotein ectodomain is composed of three domains (D) named DI, DII, and DIII, with EDIII containing virus-specific epitopes. In order to improve the serological differentiation of flavivirus infections, the recombinant soluble ectodomain of WNV E (WNV.sE) and EDIIIs (rEDIIIs) of WNV, JEV, and TBEV were synthesised using theDrosophilaS2 expression system. Purified antigens were covalently bonded to fluorescent beads. The microspheres coupled to WNV.sE or rEDIIIs were assayed with about 300 equine immune sera from natural and experimental flavivirus infections and 172 nonimmune equine sera as negative controls. rEDIII-coupled microspheres captured specific antibodies against WNV, TBEV, or JEV in positive horse sera. This innovative multiplex immunoassay is a powerful alternative to ELISAs and VNTs for veterinary diagnosis of flavivirus-related diseases.


2004 ◽  
Vol 44 (supplement) ◽  
pp. S245
Author(s):  
N Tanabe ◽  
Y Komatsuzaki ◽  
T Tsurugizawa ◽  
K Mitsuhashi ◽  
Y Ooishi ◽  
...  

2015 ◽  
Vol 28 (3) ◽  
pp. 215-220
Author(s):  
Steeve Rouillon ◽  
Claire Grignon ◽  
Nicolas Venisse ◽  
Cédric Nadeau ◽  
Marion Albouy-Llaty ◽  
...  

Résumé Il existe une relation entre exposition aux perturbateurs endocriniens (PE) et carcinogenèse animale. Cependant, les données épidémiologiques sont insuffisantes. Le bisphénol A (BPA) est un PE ubiquitaire présent dans l’eau potable. Ses dérivés chlorés (Clx-BPA) sont suspectés d’avoir une action PE 100 fois supérieure. L’objectif de ce travail était d’évaluer la faisabilité d’une étude d’exposition hydrique au BPA et aux Clx-BPA dans une population de patientes opérées du sein. L’étude a été menée au CHU de Poitiers auprès de trois populations de femmes opérées du sein classées selon la gravité de leur lésion. Trois façons d’évaluer l’exposition hydrique ont été explorées : dosage dans des matrices biologiques, dans l’eau du robinet et administration d’un questionnaire sociodémographique validé. Le critère de jugement principal était la concentration en composés dans l’eau ou les matrices biologiques et les quantités d’eau apportées par voie orale et cutanée selon le questionnaire. Dans l’eau de boisson analysée, le BPA a été quantifié chez la totalité des patientes (116 ± 162 ng∙L‑1). Les concentrations en Clx-BPA étaient de 1,85 ± 0,70 ng∙L‑1. Les concentrations urinaires en BPA étaient de 2,6 ng∙mL‑1 en préopératoire et 3,8 ± 5,5 ng∙mL‑1 en postopératoire, les Clx-BPA n’ayant pas été quantifiés. Dans le tissu adipeux mammaire, le BPA a été retrouvé à 1,265 ± 0,058 ng∙g‑1, le BPA et le Clx-BPA n’ayant été détectés qu’à deux reprises. Cette étude a montré la faisabilité des dosages du BPA et des Clx-BPA dans les matrices biologiques et l’eau du robinet. La mise en place d’une cohorte multicentrique permettra d’étudier la relation entre exposition à ces PE et cancer du sein.


2021 ◽  
pp. 113388
Author(s):  
Wonhyung Lee ◽  
Hojin Kim ◽  
Pan Kee Bae ◽  
Sanghyun Lee ◽  
Sung Yang ◽  
...  

Circulation ◽  
2008 ◽  
Vol 118 (suppl_18) ◽  
Author(s):  
Robert E Stroud ◽  
Christine N Koval ◽  
Isabelle Gengler ◽  
Anne M Deschamps ◽  
John S Ikonomidis ◽  
...  

Background. Cytokines, such as the interleukins (IL1β, IL2, IL6) and tumor necrosis factor (TNF) can modulate myocardial structure and function with ischemia/reperfusion (I/R) but dynamic assessment of these biological molecules within the human myocardial interstitium with I/R has not been performed, and the inter-relationship to matrix metalloproteinases activity (MMPact) remains unexplored. Accordingly, a fluorogenic microdialysis method was used to simultaneously measure myocardial interstitial cytokine levels and MMPact in patients during and following I/R. Methods . MMPact was measured in patients (n=13) undergoing cardio-pulmonary bypass (CPB) at baseline, during myocardial arrest and CPB (on-CPB), and immediately following reperfusion and separation from CPB (post-CPB) by a validated in-line microdialysis fluorescent detection system. Myocardial interstitial fluid was subjected to cytokine analysis by high sensitivity multiplex suspension array. Results . Interstitial MMPact increased by over 30% post-CPB and was accompanied by a specific change in cytokine profiles (Figure ). The classical pro-inflammatory molecules such as TNF and IL6 were either not detectable or unchanged, whereas IL1β and IL2 which can be proinflammatory, were increased. Conclusions. These unique results demonstrated that a dynamic cytokine signature occurs within the human myocardial interstitium following I/R and is temporally related to heightened MMP activity. Direct interrogation of the human myocardial interstitium may provide a unique insight into critical signaling pathways which may evoke adverse structural and functional events following I/R.


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