scholarly journals Corrigendum: Clotrimazole is highly effective in vitro against feline Sporothrix brasiliensis isolates

2018 ◽  
Vol 67 (3) ◽  
pp. 463-463
Author(s):  
Thalita Gagini ◽  
Luana Pereira Borba-Santos ◽  
Anderson Messias Rodrigues ◽  
Zoilo Pires de Camargo ◽  
Sonia Rozental
2017 ◽  
Vol 66 (11) ◽  
pp. 1573-1580 ◽  
Author(s):  
Thalita Gagini ◽  
Luana Pereira Borba-Santos ◽  
Anderson Messias Rodrigues ◽  
Zoilo Pires de Camargo ◽  
Sonia Rozental

HortScience ◽  
1998 ◽  
Vol 33 (3) ◽  
pp. 469a-469
Author(s):  
L.J. Skog ◽  
D.P. Murr ◽  
B.E. Digweed

Volatile compounds are ubiquitous in plants, giving fruits their characteristic aroma and flavor. There is increasing evidence that these compounds can protect plants from pathogenic organisms. In this trial ≈25 volatile compounds were tested for efficacy against Monilinia fructicola and Penicillium expansum. Both in vitro tests on agar plugs of actively growing pathogens and in situ tests on inoculated stone fruits and pears were conducted. The volatile compounds were grouped into three categories based upon fungicidal activity in vitro: highly effective (fungicidal concentration ≤100 M), moderately effective (fungicidal concentration between 100–200 M) and ineffective (fungicidal concentration >200 M). Highly effective compounds included: acetaldehyde, citral, 2-ethyl-1-hexanol, 2,exadienal, E-2-hexenal, 4-hexen-3-one, linalool, (E,E)2,4-nonadienal, E-2-nonenal, E-3-none-2-one, salicylaldehyde, and valeraldehyde. Moderately effective compounds included: (E,Z) 2,6-nonadienal, propionaldehyde, terpinene, butyl acetate, E-cinnamaldehde, hexanal, E-2-hexen-1-ol, Z-3-hexen-1-ol and isoamyl acetate. Ineffective compounds included: butyrolactone, ethanol, ethyl acetate, and methyl acetate. Effectiveness of the compounds varied with both strain and type of microorganism tested. Concentraions required for effective control were much higher when the compounds were tested on inoculated fruit. Phytotoxicity was a problem with some compounds.


2018 ◽  
Vol 18 (2) ◽  
pp. 164-171 ◽  
Author(s):  
Luana da S.M. Forezi ◽  
Luana Pereira Borba-Santos ◽  
Mariana F.C. Cardoso ◽  
Vitor F. Ferreira ◽  
Sonia Rozental ◽  
...  

Sporotrichosis is a serious public health problem in Brazil that affects human patients and domestic animals, mainly cats. Thus, the search for new antifungal agents is required also due to the emergence and to the lack of effective drugs available in the therapeutic arsenal. The aim of this study was to evaluate the in vitro antifungal profile of two synthetic series of coumarin derivatives against Sporothrix schenckii and Sporothrix brasiliensis. The three-components synthetic routes used for the preparation of coumarin derivatives have proved to be quite efficient and compounds 16 and 17 have been prepared in good yields. The inhibitory activity of nineteen synthetic coumarins derivatives 16a-i and 17a-j were evaluated against Sporothrix spp. yeasts and the most potent compounds were 16b and 17i. However, according to concentrations able to inhibit (minimum inhibitory concentrations) and kill (minimum fungicidal concentrations) the cells, 17i was more effective than 16b against Sporothrix spp. Thus, 17i exhibited good antifungal activity against S. brasiliensis and S. schenckii, suggesting that it is an important scaffold for the development of novel antifungal agents.


2022 ◽  
Vol 15 (1) ◽  
pp. 55
Author(s):  
Lais Cavalcanti dos Santos Velasco de Souza ◽  
Lucas Martins Alcântara ◽  
Pãmella Antunes de Macêdo-Sales ◽  
Nathália Faria Reis ◽  
Débora Sena de Oliveira ◽  
...  

Recently, the well-known geographically wide distribution of sporotrichosis in Brazil, combined with the difficulties of effective domestic feline treatment, has emphasized the pressing need for new therapeutic alternatives. This work considers a range of synthetic derivatives as potential antifungals against Sporothrix brasiliensis isolated from cats from the hyperendemic Brazilian region. Six S. brasiliensis isolates from the sporotrichotic lesions of itraconazole responsive or non-responsive domestic cats were studied. The minimum inhibitory concentrations (MICs) of three novel hydrazone derivatives and eleven novel quinone derivatives were determined using the broth microdilution method (M38-A2). In silico tests were also used to predict the pharmacological profile and toxicity parameters of these synthetic derivatives. MICs and MFCs ranged from 1 to >128 µg/mL. The ADMET computational analysis failed to detect toxicity while a good pharmacological predictive profile, with parameters similar to itraconazole, was obtained. Three hydrazone derivatives were particularly promising candidates as antifungal agents against itraconazole-resistant S. brasiliensis from the Brazilian hyperendemic region. Since sporotrichosis is a neglected zoonosis currently spreading in Latin America, particularly in Brazil, the present data can contribute to its future control by alternative antifungal drug design against S. brasiliensis, the most virulent and prevalent species of the hyperendemic context.


2019 ◽  
Vol 31 (2) ◽  
pp. 32-37
Author(s):  
Beatriz Mendes Roca ◽  
Vanice Rodrigues Poester ◽  
Antonella Souza Mattei ◽  
Gabriel Baracy Klafke ◽  
Ivy Bastos Ramis ◽  
...  

A técnica de microdiluição em caldo, que permite determinar a concentração inibitória mínima (CIM) dos fármacos frente aos microrganismos, é considerada padrão ouro para avaliação do perfil de suscetibilidade fúngica in vitro. Considerando que a leitura dos resultados é realizada pela visualização do crescimento fúngico, e que a utilização de indicadores de crescimento microbiano poderia otimizar essa leitura, o estudo teve como objetivo avaliar o uso da resazurina como indicador do crescimento de Sporotrhix brasiliensis em testes de microdiluição em caldo. Cinco isolados clínicos (nas fases leveduriforme e filamentosa) foram testados frente ao itraconazol (ITC – concentrações de 0,0313 a 16 µg/mL) a partir da técnica de microdiluição em caldo, utilizando a resazurina nas concentrações de 0,01% e 0,002%. A leitura dos resultados foi realizada após 24, 48 e 72 horas de incubação, e a CIM dos poços com resazurina foi considerada como sendo a menor concentração sem modificação na coloração, enquanto que a CIM do controle, foi considerada a menor concentração de fármaco capaz de inibir o crescimento fúngico. Os resultados da mudança da cor da resazurina foram comparados com os resultados sem acréscimo de resazurina. A CIM do ITC na microdiluição clássica frente aos isolados testados variou de 0,0625 a 1 µg/mL, porém, com o uso da resazurina como indicador de crescimento fúngico, independente da concentração testada, a CIM foi ≤0,0625 µg/mL. O estudo evidencia que a resazurina não é eficaz como indicador de crescimento de S. brasiliensis visto que não modificou a coloração do meio de cultivo, mesmo na presença visível de crescimento fúngico, sendo portanto contra indicada para uso em testes de suscetibilidade in vitro frente a este microrganismo.


Reproduction ◽  
2016 ◽  
Vol 151 (2) ◽  
pp. 167-177 ◽  
Author(s):  
T Leahy ◽  
J P Rickard ◽  
R J Aitken ◽  
S P de Graaf

Ram spermatozoa are difficult to capacitate in vitro. Here we describe a further complication, the unreported phenomenon of head-to-head agglutination of ram spermatozoa following dilution in the capacitation medium Tyrodes plus albumin, lactate and pyruvate (TALP). Sperm agglutination is immediate, specific and persistent and is not associated with a loss of motility. Agglutination impedes in vitro sperm handling and analysis. So the objectives of this study were to investigate the cause of sperm agglutination and potential agents which may reduce agglutination. The percentage of non-agglutinated, motile spermatozoa increased when bicarbonate was omitted from complete TALP suggesting that bicarbonate ions stimulate the agglutination process. d-penicillamine (PEN), a nucleophilic thiol, was highly effective at reducing agglutination. The inclusion of 250 μM PEN in TALP reduced the incidence of motile, agglutinated spermatozoa from 76.7±2.7% to 2.8±1.4%. It was then assessed if PEN (1 mM) could be included in existing ram sperm capacitation protocols (TALP +1 mM dibutyryl cAMP, caffeine and theophylline) to produce spermatozoa that were simultaneously capacitated and non-agglutinated. This protocol resulted in a sperm population which displayed high levels of tyrosine phosphorylated proteins and lipid disordered membranes (merocyanine-540) while remaining motile, viable, acrosome-intact and non-agglutinated. In summary, PEN (1 mM) can be included in ram sperm capacitation protocols to reduce sperm agglutination and allow for the in vitro assessment of ram sperm capacitation.


2016 ◽  
Vol 15 (6) ◽  
pp. 1417-1422 ◽  
Author(s):  
Ji-xing ZHANG ◽  
Xiao-yu WANG ◽  
Zi-zhou FENG ◽  
Xue-jun GENG ◽  
Sha-moli MU ◽  
...  

2020 ◽  
Vol 64 (4) ◽  
Author(s):  
Ruth A. Reitzel ◽  
Joel Rosenblatt ◽  
Bahgat Z. Gerges ◽  
Nylev Vargas-Cruz ◽  
Issam I. Raad

ABSTRACT Candida auris is an emerging pathogen that can cause virulent central-line-associated bloodstream infections. Catheter salvage through the eradication of biofilms is a desirable therapeutic option. We compared taurolidine and minocycline-EDTA-ethanol (MEE) catheter lock solutions in vitro for the eradication of biofilms of 10 C. auris strains. MEE fully eradicated all C. auris biofilms, while taurolidine lock partially eradicated all of the C. auris biofilms. The superiority was significant for all C. auris strains tested (P = 0.002).


Blood ◽  
1995 ◽  
Vol 85 (9) ◽  
pp. 2607-2618 ◽  
Author(s):  
BR Blazar ◽  
PA Taylor ◽  
A Panoskaltsis-Mortari ◽  
GS Gray ◽  
DA Vallera

We have developed an in vitro system in which C57BL/6 donor splenocytes are exposed to B10.BR host alloantigens in the context of deficient CD28:B7 signaling as a means of preventing graft-versus-host disease (GVHD). Although 54% to 82% of MLR alloresponse was inhibited by cytotoxic T-lymphocyte antigen 4 (CTLA4)-Ig treatment of host stimulator cells, treated splenocytes were still capable of causing GVHD when infused in vivo. By adding anti-leukocyte function antigen 1 (anti-LFA1) antibody to hCTLA4-Ig in vitro to coblock the LFA1:intercellular adhesion molecule (ICAM) signaling, splenic alloresponse was inhibited by > or = 89%, yet GVHD induction capabilities were retained. Because antigen-primed cells might be more susceptible to CD28:B7 blockade, we investigated whether hCTLA4-Ig alone, anti-LFA1 antibody alone, or the combination of both added to donor-antihost in vitro primed cells could reduce GVHD. To facilitate hyporesponsiveness induction and to block B7 and ICAM ligands that are upregulated during GVHD, these reagents were also administered to recipients post-BMT. We have shown that hCTLA4-Ig plus anti-LFA1 antibody is highly effective in preventing GVHD-induced lethality (88% to 100% of treated mice surviving versus 0% to 28% of controls surviving). For optimal prevention, both hCTLA4-Ig and anti-LFA1 must be used in vitro in the context of donor-antihost primed splenocytes and continued in vivo. This in vitro-in vivo combined approach was associated with donor engraftment, and recipients were not globally immunosuppressed. We conclude that blocking both the CD28/B7 and the LFA1:ICAM pathways are critical to effective GVHD prevention and may offer advantages to in vitro donor T-cell removal.


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