RESUMO
Streptococcosis disease caused by Streptococcus agalactiae (Group B Streptococcus, GBS) results in a huge economic loss of tilapia culture. It is urgent to find new antimicrobial agents against streptococcosis. In this study, 20 medicinal plants were evaluated in vitro and in vivo to obtain medicinal plants and potential bioactive compounds against GBS infection. The results showed that the ethanol extracts of 20 medicinal plants had low or no antibacterial properties in vitro, with a minimal inhibitory concentration ≥256 mg/L. Interestingly, in vivo tests showed that 7 medicinal plants could significantly inhibit GBS infection in tilapia, and Sophora flavescens (SF) had the strongest anti-GBS activity in tilapia, reaching 92.68%. SF could significantly reduce the bacterial loads of GBS in different tissues (liver, spleen and brain) of tilapia after treated with different tested concentrations (12.5, 25.0, 50.0 and 100.0 mg/kg) for 24 h. Moreover, 50 mg/kg SF could significantly improve the survival rate of GBS-infected tilapia by inhibiting GBS replication. Furthermore, the expression of antioxidant gene cat, immune-related gene c-type lysozyme and anti-inflammatory cytokine il-10 in liver tissue of GBS-infected tilapia significantly increased after treated with SF for 24 h. Meanwhile, SF significantly reduced the expression of immune-related gene myd88 and pro-inflammatory cytokines il-8 and il-1ß in liver tissue of GBS-infected tilapia. The negative and positive models of UPLC-QE-MS, respectively, identified 27 and 57 components of SF. The major components of SF extract in the negative model were α, α-trehalose, DL-malic acid, D- (-)-fructose and xanthohumol, while in the positive model were oxymatrine, formononetin, (-)-maackiain and xanthohumol. Interestingly, oxymatrine and xanthohumol could significantly inhibit GBS infection in tilapia. Taken together, these results suggest that SF can inhibit GBS infection in tilapia, and it has potential for the development of anti-GBS agents.
Assuntos
Ciclídeos , Doenças dos Peixes , Plantas Medicinais , Infecções Estreptocócicas , Tilápia , Animais , Sophora flavescens , Streptococcus agalactiae/genética , Doenças dos Peixes/tratamento farmacológico , Doenças dos Peixes/microbiologia , Infecções Estreptocócicas/tratamento farmacológico , Infecções Estreptocócicas/veterinária , Infecções Estreptocócicas/microbiologia , Antibacterianos/farmacologia , Antibacterianos/uso terapêutico , Tilápia/microbiologia , Citocinas , Ciclídeos/microbiologiaRESUMO
White Spot Disease (WSD), caused by white spot syndrome virus (WSSV), is an acute and highly lethal viral disease of shrimp. Currently, there are no commercially available drugs to control WSD. It is urgent and necessary to find anti-WSSV drugs. Natural compounds are an important source of antiviral drug discovery. In this study, the anti-WSSV activity of natural compound geniposide (GP) was investigated in crayfish Procambarus clarkii. Results showed that GP had a concentration-dependent inhibitory effect on WSSV replication in crayfish at 24 h, and highest inhibition was more than 98%. In addition, GP significantly inhibited the expression of WSSV immediate-early gene ie1, early gene DNApol, late gene VP28. The mortality of WSSV-infected crayfish in control groups was 100%, while it reduced by 70.0% when treated with 50 mg/kg GP. Co-incubation, pre-treatment and post-treatment experiments showed that GP could prevent and treat WSSV infection in crayfish by significantly inhibiting WSSV multiplication. Mechanistically, the syntheses of WSSV structural proteins VP19, VP24, VP26 and VP28 were significantly inhibited by GP in S2 cells. Furthermore, GP could also suppress WSSV replication by blocking the expression of antiviral immunity-related factor STAT to reduce ie1 transcription. Moreover, GP possessed anti-inflammatory and anti-oxidative activity in crayfish. Overall, GP has the potential to be developed as a preventive or therapeutic agent against WSSV infection.
Assuntos
Vírus da Síndrome da Mancha Branca 1 , Animais , Antivirais/metabolismo , Antivirais/farmacologia , Astacoidea , Iridoides/farmacologia , Taxa de Sobrevida , Vírus da Síndrome da Mancha Branca 1/fisiologiaRESUMO
Streptococcus agalactiae, also known as Group B Streptococcus (GBS), can infect humans, terrestrial animals and fish. The emergence of bacterial resistance of S. agalactiae to antibiotics leads to an urgent need of exploration of new antimicrobial agents. In the study, the antibacterial activity of natural component plumbagin (PLB) against S. agalactiae was investigated in vitro and in vivo. The results showed that the minimal inhibitory concentration (MIC) of PLB against S. agalactiae was 8 mg/L. The growth curve assay revealed that PLB could inhibit the growth of S. agalactiae. In addition, the time-killing curve showed that S. agalactiae was killed almost completely by 2-fold MIC of PLB within 12 h. Transmission electron microscopy results showed obvious severe morphological destruction and abnormal cells of S. agalactiae after treated with PLB. The pathogenicity of S. agalactiae to zebrafish was significantly decreased after preincubation with PLB for 2 h in vitro, further indicating the bactericidal activity of PLB. Interestingly, PLB could kill S. agalactiae without inducing resistance development. Furthermore, pretreatment and post-treatment assays suggested that PLB also exhibited the antibacterial activity against S. agalactiae infection in vivo by effectively reducing the bacterial load and improving the survival rate of S. agalactiae-infected zebrafish. In summary, PLB had potent antibacterial activity against S. agalactiae in vitro and in vivo, and it could be an excellent antimicrobial candidate to prevent and control S. agalactiae infection.
Assuntos
Doenças dos Peixes , Infecções Estreptocócicas , Animais , Antibacterianos/farmacologia , Doenças dos Peixes/microbiologia , Naftoquinonas , Infecções Estreptocócicas/tratamento farmacológico , Infecções Estreptocócicas/microbiologia , Infecções Estreptocócicas/veterinária , Streptococcus agalactiae , Peixe-ZebraRESUMO
Gold nanoparticles (GNPs) are one of the most widely used nanomaterials in various fields. Especially, the unique chemical and physical properties make them as the promising candidates in drug target identification, unfortunately, little is known about their application in parasites. In this paper, GNPs were employed as new solid support to identify drug targets of natural bioactive compound arctigenin (ARG) against fish monogenean parasite Gyrodactylus kobayashi. Before target identification, GNPs with ARG on the surface showed the ability to enter the live parasites even the nucleus or mitochondria, which made the bound compounds capable of contacting directly with target proteins located anywhere of the parasites. At the same time, chemically modified compound remained the anthelminthic efficacy against G. kobayashii. The above results both provide assurance on the reliability of using GNPs for drug target-binding specificity. Subsequently, by interrogating the cellular proteome in parasite lysate, myosin-2 and UNC-89 were identified as the potential direct target proteins of ARG in G. kobayashii. Moreover, results of RNA-seq transcriptomics and iTRAQ proteomics indicated that myosin-2 expressions were down-regulated after ARG bath treatment both in transcript and protein levels, but for UNC-89, only in mRNA level. Myosin-2 is an important structural muscle protein expressed in helminth tegument and its identification as our target will enable further inhibitor optimization towards future drug discovery. Furthermore, our findings demonstrate the power of GNPs to be readily applied to other parasite drugs of unknown targets, facilitating more broadly therapeutic drug design in any pathogen or disease model.
Assuntos
Furanos/metabolismo , Ouro/química , Lignanas/metabolismo , Nanopartículas Metálicas/química , Platelmintos/parasitologia , Proteoma/metabolismo , Animais , Transporte Biológico , Descoberta de Drogas , Peixes , Regulação da Expressão Gênica/efeitos dos fármacos , Mitocôndrias/metabolismo , Estrutura Molecular , Miosinas/genética , Miosinas/metabolismo , Ligação Proteica , Proteômica , RNA Mensageiro/efeitos dos fármacos , Reprodutibilidade dos Testes , Relação Estrutura-Atividade , Propriedades de SuperfícieRESUMO
Monogeneans of the genus Gyrodactylus are well-known pathogens causing huge mortalities in wild and cultured fish. Cytokine expression is one of most important host defense mechanisms against parasite infections. In this study, the expression pattern of the key pro-inflammatory (IL-1ß, IL-8, IFN-γ, TNF-α, IL-12 and iNOS) and anti-inflammatory cytokine genes (IL-10, TGFß and IL-4) of Gyrodactylus kobayashii infected goldfish (Carassius auratus) were determined by real-time quantitative PCR analysis. Our results showed that G. kobayashii infection caused increased expression of the pro-inflammatory cytokines including IFN-γ, TNF-α and iNOS in all detected tissues throughout the infection period. Among these genes, iNOS has the highest transcript level accompanied with increased nitric oxide (NO) concentration in the serum of all infected goldfish. The mRNA level of IL-1ß in the liver, spleen and head kidney was significantly up-regulated during the early stage of infection (days 2-8). While high expression level of IL-8 and IL-12 was observed during the elimination phase of infection (days 10-14). As for anti-inflammatory cytokines, the expression profiles of IL-10 were distinct from those of TGF-ß and IL-4. Specifically, the mRNA level of IL-10 did not increase in the spleen and head kidney during the early stage of infection, while increased expression of TGF-ß and IL-4 were likewise seen. Besides, all infected fish had significantly higher complement C3 but lower IgM levels than the non-infected fish. The results provide insights into the interaction between gyrodactylids and the fish host, and indicate that systemic cytokine responses are critical for controlling parasite infection in fish.
Assuntos
Citocinas/metabolismo , Doenças dos Peixes/parasitologia , Carpa Dourada , Transcriptoma , Infecções por Trematódeos/veterinária , Animais , Citocinas/genética , Doenças dos Peixes/metabolismo , Proteínas de Peixes , Trematódeos , Infecções por Trematódeos/metabolismo , Infecções por Trematódeos/parasitologiaRESUMO
White spot syndrome virus (WSSV) is a serious epidemic pathogen of crustaceans and cause severe economic losses to aquaculture. However, no commercial drugs presently available to control WSSV infection. Genipin (GN) is a bioactive compound extracted from the fruit of Gardenia jasminoides and exhibits potential antiviral activity. In the study, the antiviral activity of GN against WSSV was investigated in crayfish Procambarus clarkii and in shrimp Litopenaeus vannamei. In vitro antiviral test showed that GN could inhibit WSSV replication in crayfish and in shrimp, and the highest inhibition on WSSV was over 99% when treatment with 50â¯mg/kg of GN for 24â¯h. In vivo antiviral test proved that GN could be used to treat and prevent WSSV infection. GN could also effectively protect crayfish from WSSV infection by reducing the mortality rate of WSSV-infected crayfish. Moreover, GN attenuated the WSSV-induced oxidative stress and inflammatory by upregulation the expression of antioxidant-related genes and downregulation the expression of inflammatory-related genes, respectively. Mechanically, GN inhibited WSSV replication at least via decreasing STAT (signal transducer and activator of transcription) gene expression to block WSSV immediate-early gene ie1 transcription. Additionally, the inhibition of BI-1 (Bax inhibitor-1) gene expression also played an important role in the suppression of WSSV infection. In conclusion, GN represented a potential therapeutic and preventive agent to block WSSV infection.
Assuntos
Antivirais/farmacologia , Astacoidea/fisiologia , Iridoides/farmacologia , Penaeidae/fisiologia , Vírus da Síndrome da Mancha Branca 1/efeitos dos fármacos , Animais , Astacoidea/virologia , Relação Dose-Resposta a Droga , Penaeidae/virologia , Distribuição AleatóriaRESUMO
Intestinal bacteria play an important role in the health and provide a variety of beneficial effects to host. Immunosuppressant can reduce the immunity of host and increase the susceptibility to pathogens. But it is not clear whether the increased susceptibility caused by immunosuppressant is related to changes of gut microbiota. In this study, we used crucian carp administrated with dexamethasone to explore the effects of immunosuppressants on gut microbial communities and further evaluate the potential association between changes in gut microbiota and susceptibility to pathogens. The results of MANOVA based on the top 10 PCoA axis scores from unweighed/weighted UniFrac distances showed that administration of dexamethasone (Pâ¯=â¯0.021) and the administration time (Pâ¯=â¯0.027) had a significant impact on the gut microbial composition, regardless of pathogens infection status (Pâ¯=â¯0.35). After administration with dexamethasone, the fish had higher abundance of Cetobacterium and lower abundance of Bacillus and Lactococcus, and the abundance of genus Bacillus, Pseudomonas and Lactococcus decreased along with prolong administration time of dexamethasone. The results may help us understand the correlation between the host susceptibility to pathogenic bacteria and gut microbial community shift, and extend our knowledge regarding the role of gut microbiota in keeping the balance between pathogenic and symbiotic bacteria.
Assuntos
Bactérias/efeitos dos fármacos , Carpas/imunologia , Suscetibilidade a Doenças/microbiologia , Microbioma Gastrointestinal , Terapia de Imunossupressão/efeitos adversos , Animais , Anti-Inflamatórios/efeitos adversos , Bactérias/isolamento & purificação , Carpas/microbiologia , Dexametasona/efeitos adversos , Imunossupressores/efeitos adversos , Intestinos/imunologia , Intestinos/microbiologia , Simbiose/efeitos dos fármacosRESUMO
Many natural products from medicinal plants are small molecular weight compounds with enormous structural diversity and show various biological activities. Magnolol is a biphenol compound rich in the stem bark of Magnolia officinalis Rehd et Wils., and is able to suppress viral replication in GCRV-infected grass carp (Ctenopharyngodon idella) kidney (CIK) cells in the previous study. In this study, in vivo studies demonstrated that magnolol was efficient to restrain the replication of GCRV and repair the low level of superoxide dismutase and total antioxidant capacity in serum at the non-toxic concentration in vivo. Furthermore, magnolol inhibited CIK cell apoptosis induced by GCRV and kept the normal cellular morphological structure, reflecting in the protection of CIK cells from cell swelling, the formation of apoptotic bodies, the disappearance of cellular morphology and nuclear fragmentation. Reverse transcript quantitative polymerase chain reaction (RT-qPCR) showed that magnolol facilitated the expression of apoptosis-inhibiting gene bcl-2, while suppressed the expression of apoptosis-promoting gene bax in GCRV-infected cells. Besides, RT-qPCR and enzyme activity assays proved that magnolol suppressed the expression of caspase 3, caspase 8 and caspase 9. Moreover, interactions between magnolol and proteins were predicted by using the STITCH program, which revealed that ten proteins including caspase 3, were involved in the apoptosis pathway, p53 signaling pathway, mitogen-activated protein kinase (MAPK) signaling pathway and toll-like receptor signaling pathway. Further assays were performed to test the effect of magnolol on apoptosis pathway, which showed that magnolol dramatically inhibited the activity of caspase 3 rather than those of caspase 8 and caspase 9. Collectively, the present study revealed that magnolol heightened the resistance of grass carp against GCRV infection and refrained GCRV-induced apoptosis, which may be attributed to the direct interaction of magnolol with caspase 3. The present results make a contribution to understanding the mechanisms by which small-molecule drugs possess antiviral activities, and lay a foundation for the development of broad-spectrum antiviral compounds in aquaculture industry.
Assuntos
Antivirais/farmacologia , Apoptose , Compostos de Bifenilo/farmacologia , Carpas/imunologia , Doenças dos Peixes/imunologia , Imunidade Inata , Lignanas/farmacologia , Infecções por Reoviridae/imunologia , Animais , Linhagem Celular , Efeito Citopatogênico Viral , Doenças dos Peixes/virologia , Reoviridae/fisiologia , Infecções por Reoviridae/virologiaRESUMO
Goldfish is known to be parasitized by at least seven species of Dactylogyrus and considered as one of the most common hosts. Dactylogyrus vastator and Dactylogyrus intermedius are the dominant species living on the gills of goldfish. However, little information on morphometric characterization is available, which easily causes misidentification. The purpose of this study is to provide comprehensive morphometric and molecular characterization of D. vastator and D. intermedius collected form a fish farm in Henan, China. The characterization was presented based on the high-resolution images and standard molecular markers (18S ribosomal DNA subunit and the internal transcribed spacer region), as well as a total of 10 point-to-point morphometrics characters. In addition, a detailed comparison of morphometric and phylogenetic characterization in D. vastator versus D. intermedius was performed. The results demonstrated that all parameters measured differed significantly between these two species of Dactylogyrus, whereas molecular comparison showed subtle differences between them in nucleotide divergence and genetic distances. These findings suggested that these two species of Dactylogyrus can be distinguished more easily based on morphometric measurements than molecular data for 18S ribosomal DNA + internal transcribed spacer region (ITS-1).
Assuntos
DNA Espaçador Ribossômico/genética , Doenças dos Peixes/parasitologia , Brânquias/parasitologia , Carpa Dourada/parasitologia , Platelmintos/classificação , Animais , China , Pesqueiros , Microscopia Eletrônica de Varredura , Filogenia , Platelmintos/genética , Platelmintos/isolamento & purificação , RNA Ribossômico 18S/genéticaRESUMO
Goldfish, Carassius auratus, widely distributed across Eurasia, is one of the earliest fish domesticated for ornamental purposes. A series of diseases break out due to high-density culture of goldfish, causing significant economic losses. Here, we report for the first time an infection of Gyrodactylus kobayashii associated with the high mortality of goldfish from a fish farm in Anziying township of Henan province, China, following their transfer to several aquariums. In the first 2 weeks after goldfish (n = 4200, weight 10.24 ± 1.45 g) transfer to aquariums, a total of 3335 goldfish were lost, representing 79.4 % of the initial stocked biomass. The examination showed that no other pathogens were found in this batch of fishes, except for G. kobayashii. The high burdens of G. kobayashii/fish (264.7, range 100-450) were the primary reason for the high mortality, although this was not the sole cause. In addition, the isolate of G. kobayashii from goldfish (C. auratus) in Henan province of central China was described. The morphological characterization was performed using morphometric measurements and drawings of opisthaptoral hard parts of the parasites. The molecular description was performed based on phylogenetic analysis of a reference DNA sequence spanning 5.8S and ITS-2. Importantly, the present study provides for the first time a full 25 point-to-point morphometric measurements and high-resolution images of attachment organ of G. kobayashii.
Assuntos
Doenças dos Peixes/parasitologia , Pesqueiros , Carpa Dourada/parasitologia , Trematódeos/isolamento & purificação , Infecções por Trematódeos/veterinária , Animais , China , Doenças dos Peixes/mortalidade , Filogenia , Trematódeos/anatomia & histologia , Trematódeos/classificação , Trematódeos/genética , Infecções por Trematódeos/mortalidade , Infecções por Trematódeos/parasitologiaRESUMO
Dactylogyrus formosus Kulwiec, 1927 (Monogenea: Dactylogyridae), widely distributed across Eurasia, is considered as one of the most frequently encountered ectoparasites of goldfish (Carassius auratus). In the present study, D. formosus on gills of cultured goldfish was reported in central China for the first time, using the methods of morphological characters and molecular markers. It was characterized by "Anchoratoid-Wegeneri" type anchor with elongate inner and unobvious outer root. The morphology of the opisthaptoral hard parts of D. formosus superficially resembles species of D. arcuatus Yamaguti, 1942 parasitized crucian carp, using light and scanning electron microscopy. However, the anchor total length of D. arcuatus (range 90-102) is almost double the size of D. formosus (range 43.7-57.1) which allows for their rapid discrimination from each other; on the other hand, the two species also can be easily separated by the shape of the male copulatory organ. The morphological description of D. formosus is supplemented with phylogenetic analysis of a reference DNA sequence spanning 18S rDNA and ITS1. What is more, this study also redescribes comprehensively D. formosus, providing for the first time a full ten point-to-point morphometric measurements of the hard parts, and importantly, a photographic record of the armature of the haptor and the male copulatory organ.
Assuntos
Infecções por Cestoides/veterinária , Doenças dos Peixes/parasitologia , Carpa Dourada/parasitologia , Platelmintos/parasitologia , Animais , Infecções por Cestoides/parasitologia , China , DNA Ribossômico/genética , Feminino , Brânquias/parasitologia , Masculino , Dados de Sequência Molecular , Filogenia , Platelmintos/classificação , Platelmintos/genética , Platelmintos/isolamento & purificaçãoRESUMO
Dactylogyrus spp. and Gyrodactylus spp. are helminth ectoparasites that are a significant threat to the aquaculture industry. Existing treatments could cause the threats of anthelmintic resistance, risk of residues, environmental contamination, and toxicity to fish. Importantly, there is no report on a treatment against these two parasites. This study explored the possibility of using the extracts of Santalum album to treat Dactylogyrus sp. and Gyrodactylus sp. infections in goldfish. Results showed that among the four extracts (chloroform, methanol, ethyl acetate, and water) of S. album, the chloroform extract is the most effective and 40 mg/L is a safe and the lowest effective dosage. In addition, we found that Gyrodactylus elegans is more sensitive than Dactylogyrus intermedius when exposed to the extract of the medicinal plant. Finally, it is substantiated that bath treatment with long duration and multiple administrations could eliminate a greater proportion of monogenean infections. These findings show the potential for the development of effective and safe therapy to treat Dactylogyrus sp. and Gyrodactylus sp. infections of fishes.
Assuntos
Anti-Helmínticos/farmacologia , Doenças dos Peixes/parasitologia , Carpa Dourada , Magnoliopsida/química , Santalum/química , Infecções por Trematódeos/veterinária , Animais , Anti-Helmínticos/química , Doenças dos Peixes/tratamento farmacológico , Extratos Vegetais/química , Extratos Vegetais/farmacologia , Trematódeos/efeitos dos fármacos , Infecções por Trematódeos/tratamento farmacológicoRESUMO
With the aim of finding natural anthelmintic agents against Dactylogyrus intermedius (Monogenea) in goldfish (Carassius auratus), 26 plants were screened for antiparasitic properties using in vivo anthelmintic efficacy assay. The results showed that Caesalpinia sappan, Lysima chiachristinae, Cuscuta chinensis, Artemisia argyi, and Eupatorium fortunei were found to have 100% anthelmintic efficacy at 125, 150, 225, 300, and 500 mg L(-1) after 48 h of exposure. Crude extract of the five plants were further partitioned with petroleum ether, chloroform, ethyl acetate, methanol, and water to obtain anthelmintically active fractions with various polarity. Among these fractions tested, the ethyl acetate extract of L. chiachristinae was found to be the most effective with a 50% effective concentration (EC50) value of 5.1 mg/L after 48 h of exposure. This was followed by ethyl acetate extract of C. chinensis (48 h-EC50 = 8.5 mg L(-1)), chloroform extracts of C. sappan (48 h-EC50 = 15.6 mg L(-1)), methanol extract of C. chinensis (48 h-EC50 = 15.9 mg L(-1)), and chloroform and petroleum ether extract of L. chiachristinae (EC50 values of 17.2 and 21.1 mg/L, respectively), suggesting that these plants, as well as the active fractions, provide potential sources of botanic drugs for the control of D. intermedius in aquaculture.
Assuntos
Anti-Helmínticos/farmacologia , Doenças dos Peixes/tratamento farmacológico , Carpa Dourada/parasitologia , Extratos Vegetais/farmacologia , Plantas Medicinais/química , Trematódeos/efeitos dos fármacos , Animais , Anti-Helmínticos/uso terapêutico , Aquicultura , Descoberta de Drogas , Doenças dos Peixes/parasitologia , Extratos Vegetais/uso terapêuticoRESUMO
Ichthyophthirius multifiliis (also called "ich") is an external protozoan parasite that may infest almost all freshwater fish species and caused significant economic damage to the aquaculture industry. Since the use of malachite green was banned, there have been relatively few effective alternative strategies for controlling I. multifiliis infections. The present study was designed to screen potential antiparasitic medicinal plants based on our previous studies, and comprehensively evaluate in vitro and in vivo anti-ich activity of selected plant extracts. The screening results showed that the methanol extract of Psoralea corylifolia had the highest activity against I. multifiliis theronts. In vivo theront trials demonstrated that 1.25 mg/L or more concentrations of P. corylifolia methanol extract caused 100 % mortality during the 4-h exposure period, and the subsequent in vitro trials indicated that the minimum concentration of P. corylifolia methanol extract that prevented the initial infestation was 2.50 mg/L. Protomonts and encysted tomonts surviving trials suggested that encysted tomonts were less susceptible to P. corylifolia methanol extract than protomonts, and the methanol extract of P. corylifolia at a concentration of 5.00 mg/L could kill 100 % of protomonts and 88.89 % of encysted tomonts. It was also observed that after 12-h exposure of protomonts or encysted tomonts to 2.50 mg/L of P. corylifolia methanol extract, the theronts emerged from encysted tomonts led to more infection level than the ones in the other groups. The results suggested that whether the protomonts finish encystment is crucial to the survival, reproduction, and theronts infectivity. In addition, our results showed that long duration (24 h) and high concentration (5.00 mg/L) significantly reduced the survival and reproduction of I. multifiliis tomont exited from the fish after in-bath treatment, and it is indicated that P. corylifolia methanol extract had a potential detrimental effect on I. multifiliis trophont in situ.
Assuntos
Antiprotozoários/farmacologia , Infecções por Cilióforos/veterinária , Misturas Complexas/farmacologia , Doenças dos Peixes/tratamento farmacológico , Hymenostomatida/efeitos dos fármacos , Plantas Medicinais/química , Psoralea/química , Animais , Antiprotozoários/isolamento & purificação , Sobrevivência Celular/efeitos dos fármacos , Infecções por Cilióforos/tratamento farmacológico , Infecções por Cilióforos/parasitologia , Misturas Complexas/isolamento & purificação , Avaliação Pré-Clínica de Medicamentos/métodos , Doenças dos Peixes/parasitologia , Carpa Dourada , Testes de Sensibilidade ParasitáriaRESUMO
Virus-induced central nervous system (CNS) diseases represent a significant burden to animal health worldwide. The difficulty in treating these diseases is mainly attributable to the elaborate barrier system, which limits the transport of drugs to the infected sites. Therefore, it is necessary to develop smart delivery technologies for treatment of these diseases. In the study, viral nervous necrosis disease was studied as a model to evaluate the feasibility of multiwalled carbon nanotubes (MWCNTs) conjugated with virus-specific nanobody and antiviral drug for targeted therapy of virus-induced CNS diseases. The virus (named as PGNNV) was isolated, identified and purified from diseased grouper. A naïve phage-displayed alpaca nanobody library was constructed, and the purified PGNNV was used for biopanning of PGNNV-specific nanobody from the library. The targeted delivery system based on MWCNTs conjugated with polyethylenimine, ribavirin, and PGNNV-specific nanobody was constructed and designated as MWCNTs-PEI-R-Nb. Targeting ability and treatment effects of the MWCNTs-PEI-R-Nb were checked both in vitro and in vivo. MWCNTs-PEI-R-Nb showed an increasing distribution in PGNNV-infected cells, and an obvious accumulation in the brain of PGNNV-infected zebrafish larvae. MWCNTs-PEI-R-Nb also showed a strong anti-PGNNV ability both in vitro and in vivo. The mortality of larvae treated with MWCNTs-PEI-R-Nb (equivalent to 100 mg/L ribavirin) was 27% during 10 days post infection, whereas it was 100% for the control group. The results so far indicate that MWCNTs conjugated with antiviral drugs and viral-specific antibody are effective means for virus-induced CNS disease targeted therapy.
Assuntos
Doenças do Sistema Nervoso Central/tratamento farmacológico , Doenças do Sistema Nervoso Central/virologia , Portadores de Fármacos/química , Sistemas de Liberação de Medicamentos , Nanotubos de Carbono/química , Vírus/metabolismo , Animais , Linhagem Celular , Larva/virologia , Vírus/isolamento & purificação , Vírus/ultraestrutura , Peixe-Zebra/virologiaRESUMO
As a successful prevention strategy for controlling the highly contagious and pathogenic disease of spring viremia of carp (SVC), DNA vaccines reported in recent years could trigger protective responses against SVC with the means of injection. However, there remains many concerns and uncertainties related to DNA vaccination as well as injection is labor intensive, costly and not suitable to vaccinate large numbers of fish. Therefore, more efficient and safe prophylactic measures should be urgently investigated. In this research, single-walled carbon nanotubes (SWCNTs) as the candidate SWCNTs-pET32a-G subunit vaccine carrier were administrated via bath (1, 5, 10, 20, 40â¯mgâ¯L-1) or injection (1, 4, 8, 12, 20⯵g) in common carp juvenile, and the different immune treatments to induce immunoprotective effect were analyzed. The results showed that SWCNTs-pET32a-G could enter fish body after immersion for 10â¯h, furthermore, compared to control groups, antibody levels, the non-specific immune parameters (complement activity, superoxide dismutase activity and alkaline phosphatase activity), and immune-related genes (especially the TNF-α and IFNg2b) in vaccinated groups were significantly enhanced in fish immunized with SWCNTs-subunit vaccine. In addition, as a promising carrier, SWCNTs can increase the immune protective effect of naked subunit vaccine by ca. 16% in bath immunization group and by ca. 23% in injection group. This study suggests that SWCNTs-vaccine may represent a potentially efficient immersion vaccine against viral pathogens of fish in the future.
Assuntos
Nanotubos de Carbono/química , Vacinas Virais/química , Vacinas Virais/uso terapêutico , Viremia/imunologia , Viremia/prevenção & controle , Animais , Carpas , Doenças dos Peixes/imunologia , Doenças dos Peixes/prevenção & controle , ImunizaçãoRESUMO
Using Saccharomyces cerevisiae as an experimental model, the potential toxicological effects of oxidized multi-walled carbon nanotubes (MWCNTs) were investigated following exposure to 0-600mg/L for 24h. Results indicated that MWCNTs (>100mg/L) had adverse effects on the cell proliferation. MWCNTs were clearly visible in lysosome, vacuole, endosome, mitochondria, multivesicular body and localization in the perinuclear region. The uptake kinetics data demonstrated that the maximum MWCNTs content (209.61mg/g) was reached at 3h, and a steady state was reached after 18h. Based on the combined results of transmission electron microscope, endocytosis inhibition experiments and endocytosis-related genes (END3, END6, Sla2 and Rsp5) expression analysis, we elucidated MWCNTs uptake mechanism: (i) via a direct penetration of single MWCNTs; (ii) via endocytosis of single MWCNTs; and (iii) via endocytosis of MWCNTs aggregates. The percentage of apoptosis was significant increased at 600mg/L. The decrease of mitochondrial transmembrane potential and the leakage of cytochrome c shown dose-dependent manners. Interestingly, there was no significant increase of reactive oxygen species (ROS). The apoptosis-related genes (SOD1, SOD2, Yca1, Nma111 and Nuc1) were significant changed. These results obtained in our study demonstrated that oxidized MWCNTs induce Saccharomyces cerevisiae apoptosis via mitochondrial impairment pathway.
Assuntos
Nanotubos de Carbono/toxicidade , Saccharomyces cerevisiae/efeitos dos fármacos , Saccharomyces cerevisiae/metabolismo , Apoptose/efeitos dos fármacos , Proteínas Reguladoras de Apoptose/metabolismo , Citocromos c/metabolismo , Relação Dose-Resposta a Droga , Endocitose/efeitos dos fármacos , Cinética , Potencial da Membrana Mitocondrial/efeitos dos fármacos , Mitocôndrias/efeitos dos fármacos , Espécies Reativas de Oxigênio/metabolismo , Saccharomyces cerevisiae/ultraestruturaRESUMO
Using Tetrahymena thermophila as experimental models, the oxidative stress of triazole fungicides myclobutanil (MYC) and cyproconazole (CYP) was investigated. Results showed that 24-h EC50 values for MYC and CYP were 16.67 (13.37-19.65) and 20.44 (18.85-21.96) mg/L, respectively; 48-h EC50 values for MYC and CYP were 14.31 (13.13-15.42) and 18.76 (17.09-20.31) mg/L, respectively. Reactive oxygen species was significantly induced and cytotoxicity was caused by MYC and CYP by increasing propidium iodide (PI) fluorescence. Damage of regular wrinkles and appearing of small holes on the cell surface were observed by SEM. Furthermore, MYC and CYP also caused notable changes in enzyme activities and mRNA levels. Overall, the present study points out that MYC and CYP lead to oxidative stress on T. thermophila. The information presented in this study will provide insights into the mechanism of triazoles-induced oxidative stress on T. thermophila.
Assuntos
Nitrilas/toxicidade , Espécies Reativas de Oxigênio/metabolismo , Tetrahymena thermophila/efeitos dos fármacos , Triazóis/toxicidade , Membrana Celular/efeitos dos fármacos , Fígado/efeitos dos fármacos , Testes de Sensibilidade Microbiana , Estresse Oxidativo , Testes de ToxicidadeRESUMO
Ichthyophthirius multifiliis, an external fish parasite, often causes significant economic damage to the aquaculture industry. Since the use of malachite green was banned, the search of alternative substance to control I. multifiliis infections becomes stringent. In present study, in vitro and in vivo anti-ich efficacies of isopsoralen and psoralidin, two active compounds isolated from methanol extract of Psoralea corylifolia by bioassay-guided fractionation based on the efficacy of anti-ich encysted tomonts, were evaluated. In vitro antiprotozoal efficacy of psoralidin is much better than that of isopsoralen. Psoralidin can kill all theronts at concentrations of 0.8 mg/L or more during 4 h exposure; and terminate reproduction of I. multifiliis post 6 h exposure of protomonts to 0.9 mg/L and encysted tomonts to 1.2 mg/L. In vivo trials showed that 5 h exposure of infected fish to 2.5 mg/L of psoralidin significantly reduced the number of theronts released from tomonts. Furthermore, we observed that a part of protomonts, collected from infected fish post treatment, presented characteristic morphological changes of apoptosis after staining with Annexin V-EGFP/propidium iodide, indicating the possible mechanism of psoralidin against I. multifiliis trophont in situ. On the basis of these results, psoralidin can be used as a potential lead compound for the development of commercial drug against I. multifiliis.
Assuntos
Benzofuranos/farmacologia , Infecções por Cilióforos/veterinária , Cumarínicos/farmacologia , Doenças dos Peixes/parasitologia , Furocumarinas/farmacologia , Hymenostomatida/efeitos dos fármacos , Psoralea/química , Animais , Antiprotozoários/administração & dosagem , Antiprotozoários/química , Antiprotozoários/farmacologia , Benzofuranos/administração & dosagem , Benzofuranos/química , Infecções por Cilióforos/tratamento farmacológico , Infecções por Cilióforos/parasitologia , Cumarínicos/administração & dosagem , Cumarínicos/química , Relação Dose-Resposta a Droga , Furocumarinas/administração & dosagem , Furocumarinas/química , Carpa Dourada , Estrutura MolecularRESUMO
OBJECTIVE: To investigate the surgical timing and effects for vitreous hemorrhage caused by blunt ocular trauma. METHOD: 116 eyes of vitreous hemorrhage caused by ocular blunt trauma were divided into two groups, non-vitrectomy group (46 eyes) and vitrectomy group (70 eyes). The treating results and follow-up results were compared. RESULTS: 50 of 70 eyes (71.4%) in vitrectomy group and 10 of 46 eyes (21.7%) in non-vitrectomy group achieved a visual acuity of 0.1 or better over a follow-up period of 1 month, which indicated a significant difference between two groups. In the non-vitrectomy group, visual acuity of 10 eyes were better than 0.1, 7 eyes (70.0%) of them improved within 2 weeks of injury. In surgery group, 27.1% underwent only vitrectomy and 70.9% needed combining with other manipulations. In vitrectomy group the retina detachment was found in 3 eyes (4.3%) post-operatively and were cured by second operation. In non-vitrectomy group, the retinal detachment was found in 14 eyes (30.4%) during the follow-up period, and 8 eyes (72.7%) of 11 eyes received operation were cured. CONCLUSION: Early vitreous surgery can improve curative effect for vitreous hemorrhage caused by blunt ocular trauma when no improvement was observed after applied drugs 2 - 3 weeks.