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Efficacy and safety of praziquantel in the treatment of neurocysticercosis in Vietnam. 吡喹酮治疗越南神经囊虫病的疗效和安全性。
IF 0.8 4区 医学 Q4 PARASITOLOGY Pub Date : 2022-09-01 DOI: 10.47665/tb.39.3.018
T D Thang, T Q Phuc, D T Thanh, N Q Thieu, T H Tho, C B Loi, L Tran-Anh

Neurocysticercosis (NCC) is a parasitic infection of the nervous system and is responsible for considerable morbidity and mortality. Praziquantel (PZQ) is one of the antiparasitics mostly used in managing NCC, however, there have been only a few studies on the treatment outcome of this drug. The present study aimed to evaluate the efficacy and safety of PZQ in patients with NCC. Sixty patients with typical characteristics of NCC received three 10-day cycles of PZQ and the interruption between these cycles was 10 days. Additional treatment included antiinflammation (steroids), antiepileptics and analgesics. Clinical and imaging studies were done at baseline and six months after therapy to assess the efficacy of treatment. Laboratory evaluation was done before and after each cycle to investigate laboratory safety profiles. By six months after finishing therapy, all patients had clinical improvement and 75% of them were free of symptoms. The rates of complete, partial or no resolution of cysts on brain magnetic resonance imaging were 61.7%, 28.3% and 10% respectively. The efficacy of therapy was not associated with the number of cysts. There was no difference between the levels of aspartate aminotransferase, alanine aminotransferase, urea and creatinine before and after treatment. Conclusion: Praziquantel is effective and safe in the treatment of patients with neurocysticercosis.

神经囊虫病(NCC)是一种神经系统的寄生虫感染,具有相当高的发病率和死亡率。吡喹酮(Praziquantel, PZQ)是治疗NCC最常用的抗寄生虫药之一,但对其治疗效果的研究较少。本研究旨在评价PZQ对NCC患者的疗效和安全性。60例具有典型NCC特征的患者接受3个10天周期的PZQ治疗,每个周期之间的间隔为10天。其他治疗包括抗炎(类固醇)、抗癫痫药和镇痛药。临床和影像学研究分别在基线和治疗后6个月进行,以评估治疗效果。在每个周期之前和之后进行实验室评估,以调查实验室安全概况。治疗结束后6个月,所有患者均有临床改善,75%的患者症状消失。脑磁共振成像显示囊肿完全、部分和无分辨率分别为61.7%、28.3%和10%。治疗效果与囊肿数量无关。治疗前后天冬氨酸转氨酶、丙氨酸转氨酶、尿素、肌酐水平差异无统计学意义。结论:吡喹酮治疗神经囊虫病有效、安全。
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引用次数: 1
Evaluation of antitrypanosomal properties and apoptotic effects of ochrolifuanine from Dyera costulata (Miq.) Hook.f against Trypanosoma brucei brucei. 菟丝子(Dyera costulata, Miq)嗜铬柳氨酸抗锥虫特性及凋亡作用的研究钩。抗布氏锥虫。
IF 0.8 4区 医学 Q4 PARASITOLOGY Pub Date : 2022-09-01 DOI: 10.47665/tb.39.3.003
I Norhayati, Z A Nurhayati, K Getha, J Muhd Haffiz, M R Adiratna

Trypanosoma brucei parasites are flagellated kinetoplastid protozoan which is responsible for Human African Trypanosomiasis (HAT). Current chemotherapy drugs have a number of side effects and drug resistance has emerged as a major issue in current treatment. Active bisindole alkaloid compound ochrolifuanine was previously isolated from the leaves of Dyera costulata. In vitro antitrypanosomal activity of ochrolifuanine against Trypanosoma brucei brucei strain BS221 showed strong activity with an IC50 value of 0.05 ± 0.01 µg/ml. We compared the effect of ochrolifuanine and reference compound staurosporine in T. b. brucei apoptosis. The apoptosis-inducing activity of ochrolifuanine was evaluated using TUNEL assay and cell cycle analysis. Trypanosoma brucei brucei was shown to undergo apoptotic cells death as demonstrated by the appearance of several conical hallmarks of apoptosis. Ochrolifuanine was found to induce apoptosis in parasites in a dose- and time-dependent manner. The cell cycle study revealed 0.025 and 0.05 µg/ml of ochrolifuanine arrested the growth of T. b. brucei at two different growth phases (G0/G1 and in S phases). While at concentration 0.10 µg/ml arrested at the G2/M phase. In conclusion, the results indicate that ochrolifuanine displayed an antitrypanosomal effect on T. b. brucei by inducing apoptosis cell death and causing the arrest of parasite cells at different growth phases. The results suggested that ochrolifuanine may be a promising lead compound for the development of new chemotherapies for African trypanosomiasis.

布鲁氏锥虫寄生虫是一种鞭毛动质体原虫,是导致非洲人类锥虫病(HAT)的罪魁祸首。目前的化疗药物有许多副作用,耐药性已成为当前治疗的一个主要问题。从菟丝子叶中分离到活性双吲哚类生物碱化合物ochrolifuanine。结果表明,嗜铬柳氨酸对布氏锥虫菌株BS221的体外抗锥虫活性较强,IC50值为0.05±0.01µg/ml。我们比较了氯丙氨酸和参比化合物星孢素对布鲁氏杆菌凋亡的影响。采用TUNEL法和细胞周期法对嗜铬柳氨酸的诱导凋亡活性进行评价。布鲁氏锥虫具有凋亡细胞死亡的过程,其凋亡的几个圆锥形特征证明了这一点。结果表明,Ochrolifuanine诱导寄生虫细胞凋亡具有剂量依赖性和时间依赖性。细胞周期研究表明,0.025和0.05µg/ml的ochrolifuanine在两个不同的生长阶段(G0/G1期和S期)抑制了布氏杆菌的生长。当浓度为0.10µg/ml时,停留在G2/M相。综上所述,嗜铬柳氨酸对布氏锥虫具有抗锥虫作用,其机制是诱导细胞凋亡死亡,并在不同生长阶段引起细胞阻滞。这些结果表明,ochrolifuanine可能是开发新的非洲锥虫病化疗药物的有希望的先导化合物。
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引用次数: 1
Anti-Newcastle Disease Virus activity of 3β and 3α Friedelanol Triterpenoids from the leaves of Synadenium glaucescens Pax. 青合木叶中3β和3α弗里德醇三萜抗新城疫病毒活性的研究
IF 0.8 4区 医学 Q4 PARASITOLOGY Pub Date : 2022-06-01 DOI: 10.47665/tb.39.2.016
D Credo, F P Mabiki, F Machumi, M Chacha, C Cornett, B Styrishave

Newcastle Disease (ND) is a highly pathogenic disease of avian species which is caused by Newcastle Disease Virus (NDV). It is one of the major causes of mortality and morbidity to poultry industry in the third world countries. Currently, there is no treatment measures against ND; the only existing measure is vaccination, though it is incapable to offer 100% immunity. In Tanzania, the leaves of Synadenium glaucescens Pax. are traditionally used for treatment of various ailments including ND. Previously, its leaves extract has been scientifically confirmed to exhibit anti-NDV activity though bioactive compound(s) responsible for this activity is/are unknown. Therefore, this study was aimed to evaluate anti-NDV activity of 3β-Friedelanol (1) and 3α-friedelanol (2) isolated from its leaves extract. Isolation of these compounds was achieved by column chromatography method whereas, their chemical structures were determined by Nuclear Magnetic Resonance (NMR) data and by comparing with the available literature NMR data. Anti-NDV activity study was done in embryonated chicken eggs (ECEs). Treatment of NDV inoculated ECEs with 3β-Friedelanol (1) reduced the viral load to zero and maintained the survival of embryos, this was revealed by continuous organs formation and increase in embryo weights with no significant different (p > 0.05) from un-inoculated ECE. These effects suggest that, 3β-Friedelanol (1) possesses anti-NDV activity. Therefore, existence of 3β-Friedelanol (1) in the leaves of S. glaucescens may justify its earlier described anti-NDV activity and traditional use in the treatment of ND. Hence, its leaves extract may be considered for development of anti-NDV herbal formulation while 3β-Friedelanol could either serve as a drug or lead compound for synthesis of anti-NDV drugs.

新城疫病是由新城疫病毒(NDV)引起的禽类高致病性疫病。它是第三世界国家家禽业死亡和发病的主要原因之一。目前,没有针对ND的治疗措施;现有的唯一措施是接种疫苗,尽管它无法提供100%的免疫力。在坦桑尼亚,海合子的叶子。传统上用于治疗包括ND在内的各种疾病。此前,其叶提取物已被科学证实具有抗ndv活性,但这种活性的生物活性化合物尚不清楚。因此,本研究旨在评价从其叶提取物中分离得到的3β-弗里德兰醇(1)和3α-弗里德兰醇(2)的抗ndv活性。这些化合物通过柱层析法分离得到,而它们的化学结构是通过核磁共振(NMR)数据和与现有文献核磁共振数据的比较来确定的。对鸡胚蛋(ECEs)进行了抗新城疫病毒活性研究。用3β-弗里德拉醇(1)处理接种了NDV的雏鸡后,病毒载量降至零,维持了胚胎的存活,这可以通过器官的持续形成和胚胎重量的增加来证明,但与未接种雏鸡相比差异不显著(p > 0.05)。这些作用表明,3β-弗里德兰醇(1)具有抗ndv活性。因此,S. glaucescens叶片中3β-Friedelanol(1)的存在可能证明了其早期描述的抗ndv活性及其在ND治疗中的传统应用。因此,其叶提取物可考虑开发抗新城疫中药制剂,而3β-弗里德兰醇既可作为药物,也可作为抗新城疫药物合成的先导化合物。
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引用次数: 4
Renocila richardsonae Williams & Bunkley-Williams, 1992 (Isopoda: Cymothoidae), a parasite of Japanese goatfish, Upeneus japonicus off Sarawak, South China Sea. 中国南海沙捞越山山羊的一种寄生生物,reocila richardsonae Williams & Bunkley-Williams, 1992。
IF 0.8 4区 医学 Q4 PARASITOLOGY Pub Date : 2022-06-01 DOI: 10.47665/tb.39.2.014
B C Kua, M Jamil, N L Bruce

Renocila richardsonae Williams & Bunkley-Williams, 1992 is recorded for the first time from Sarawak coastal waters. During a survey of marine fishes at depth of 200 metres in South China Sea, off the coast of Sarawak from 3° to 5°N and 110° to 111°E, five specimens of Renocila richardsonae were collected from Japanese goatfish, Upeneus japonicus (Houttuyn, 1782) (Mullidae) with average prevalence of 17% and mean intensity of one isopod per fish from examination of 64 fish. The isopod was observed to cause tissue damage on the site of attachment to the host.

reocila richardsonae Williams & Bunkley-Williams, 1992年首次在沙捞越沿海水域被记录。在南中国海沙捞越海岸3°~ 5°N和110°~ 111°E海域200米深度的海洋鱼类调查中,从日本山山羊鱼(Upeneus japonicus, Houttuyn, 1782) (Mullidae)中采集到5个richardreocila,平均流行率为17%,平均强度为每条鱼1只等足类。观察到等足类动物在附着于寄主的部位造成组织损伤。
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引用次数: 0
Usefulness of the outer membrane proteins of Shigella sonnei in developing an antibody-based immunoassay for the diagnosis of shigellosis. sonnei志贺氏菌外膜蛋白在开发基于抗体的诊断志贺氏菌病的免疫测定中的作用。
IF 0.8 4区 医学 Q4 PARASITOLOGY Pub Date : 2022-06-01 DOI: 10.47665/tb.39.2.015
N N F N Mahadi, C Y Leow, K K Banga Singh

Conventional culture method and biochemical tests remain as the 'gold standard' method for the identification of S. sonnei which are time-consuming. We have discovered previously the potential of three OMPs of S. sonnei (33.3 kDa, 43.8 kDa and 100.3 kDa) as biomarkers in the diagnostic test for shigellosis. Here, we evaluated the performance of the outer membrane proteins of S. sonnei for the development of an antibody-based immunoassay for the detection of S. sonnei infections. All threetarget proteins were specifically recognized when probed with S. sonnei sera. In addition, another two potential proteins of molecular weight 29.0 kDa and 88.2 kDa in size were also exclusively recognized by the IgA when probed with S. sonnei sera. The optimized ELISA demonstrated higher sensitivity and specificity which exceeded 86.0%. In conclusion, the identified target proteins showed great potential as diagnostic biomarkers for the detection of S. sonnei infections in patients.

传统的培养方法和生物化学试验仍然是鉴定sonnei的“金标准”方法,但耗时长。我们之前已经发现sonnei s的三种OMPs (33.3 kDa, 43.8 kDa和100.3 kDa)在志贺氏菌病诊断试验中作为生物标志物的潜力。在这里,我们评估了sonnei的外膜蛋白的性能,以开发一种基于抗体的免疫分析法来检测sonnei感染。这三种靶蛋白在sonnei链球菌血清中均被特异性识别。此外,另外两个分子量为29.0 kDa和88.2 kDa的潜在蛋白在sonnei链球菌血清中也被IgA特异性识别。优化后的酶联免疫吸附试验具有较高的灵敏度和特异性,特异度均超过86.0%。综上所述,所鉴定的靶蛋白具有作为sonnei链球菌感染诊断标志物的巨大潜力。
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引用次数: 0
Therapeutic potential of royal jelly to control Toxoplasma gondii infection in mice. 蜂王浆控制小鼠刚地弓形虫感染的治疗潜力。
IF 0.8 4区 医学 Q4 PARASITOLOGY Pub Date : 2022-06-01 DOI: 10.47665/tb.39.2.020
N A Althobaiti

At present, there are several synthetic medications for toxoplasmosis therapy; however, these agents cannot be permanently applied because of adverse side effects or therapeutic failures and drug resistance in parasites. The present experimental investigation was aimed to study the effects of royal jelly (RJ) obtained from Apis mellifera in comparison with atovaquone against Toxoplasma gondii infection in mice. After treatment of infected mice with RJ at the doses of 200, 400, and 600 mg/kg for 14 consecutive days, we evaluated the therapeutic activity of RJ by measuring the mean number and the mean size of T. gondii tissue cysts, oxidant-antioxidant enzymes, pro-inflammatory cytokines, the mRNA expression levels of bradyzoite surface antigen 1 (BAG1), as well as the toxic effect on liver and kidney function. Treatment of the infected mice with RJ significantly (p < 0.001) decreased the mean number and the mean diameter of T. gondii tissue cysts and downregulated BAG1 in a dose-dependent response. After treatment of infected mice with RJ, the level of oxidative stress markers was significantly diminished, but a significant increase (p < 0.05) in the level of antioxidant markers such as glutathione peroxidase (GPx) and superoxide dismutase (SOD) enzymes was observed. Treatment of the infected mice with RJ significantly enhanced the level of pro-inflammatory cytokines IFN-γ and IL-1β, whereas it caused no substantial change in the serum levels of liver and kidney enzymes. The findings of this in vivo study revealed the favorable therapeutic effect of RJ on latent T. gondii infection in mice. It was found that RJ considerably inhibited the infection by decreasing the number and size of tissue cysts, reducing oxidative stress, and boosting the level of pro-inflammatory cytokines, but had no significant toxic impact on the function of vital organs such as liver and kidney. However, additional surveys are required to confirm these findings and clarify the exact mechanisms and their efficiency in clinical subjects.

目前,治疗弓形虫病的合成药物有几种;然而,由于寄生虫的不良副作用或治疗失败和耐药性,这些药物不能永久应用。本实验旨在研究蜜蜂蜂王浆与阿托伐醌对刚地弓形虫感染小鼠的作用。以200、400和600 mg/kg剂量的RJ连续14天治疗感染小鼠后,我们通过测量弓形虫组织囊肿的平均数量和平均大小、氧化-抗氧化酶、促炎细胞因子、慢速子表面抗原1 (BAG1) mRNA表达水平以及对肝肾功能的毒性作用来评估RJ的治疗活性。用RJ治疗感染小鼠后,弓形虫组织囊肿的平均数量和平均直径显著减少(p < 0.001),并呈剂量依赖性下调BAG1。RJ感染小鼠后,氧化应激标志物水平显著降低,抗氧化标志物如谷胱甘肽过氧化物酶(GPx)和超氧化物歧化酶(SOD)水平显著升高(p < 0.05)。用RJ治疗感染小鼠可显著提高促炎细胞因子IFN-γ和IL-1β的水平,而血清中肝脏和肾脏酶的水平无明显变化。体内实验结果表明,RJ对小鼠潜伏性弓形虫感染有良好的治疗作用。结果发现,RJ通过减少组织囊肿的数量和大小,降低氧化应激,提高促炎细胞因子水平,显著抑制感染,但对肝、肾等重要器官的功能无明显毒性影响。然而,需要更多的调查来证实这些发现,并澄清其在临床受试者中的确切机制和效率。
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引用次数: 0
First detection of Babesia sp. in Bornean sun bear (Helarctos malayanus euryspilus Horsfield) in Sabah, Malaysia. 马来西亚沙巴的第一个发现是马来西亚博尔南太阳熊的Babesia sp (Helarctos malaanus euryspilus Horsfield)。
IF 0.8 4区 医学 Q4 PARASITOLOGY Pub Date : 2022-06-01 DOI: 10.47665/tb.39.2.003
T H Chua, B N Yeoh, B O Manin, S T Wong

The Bornean sun bear, a subspecies of the endangered Malayan sun bear, resides only on Borneo Island and little is known about diseases or parasites that may impact their health. In 2019, blood and ticks were collected from 46 captive bears held at the Bornean Sun Bear Conservation Centre in Sabah, Malaysia during annual health examinations in response to previous blood smear analysis that revealed presumptive haemoparasites in more than half the resident bears. Polymerase chain reaction detected a unique Babesia sp. in one of the bears. Disease surveillance of mosquitoes trapped along the outer perimeter of the bears' outdoor enclosure did not reveal any malaria parasites. This research marks the first documented case in Bornean sun bears of both a Babesia sp. and the Ixodes tick Haemaphysalis nr koningsbergeri. More research on incriminating the vector and the effects of Babesia infection on the health of Bornean sun bears is needed. Due to the zoonotic nature of babesiosis, mitigative actions should be taken to protect any humans that work with or come into close contact with these captive bears or their enclosures.

婆罗洲马来熊是濒临灭绝的马来亚马来熊的一个亚种,只生活在婆罗洲岛,人们对可能影响它们健康的疾病或寄生虫知之甚少。2019年,在马来西亚沙巴州婆罗洲马来熊保护中心进行年度健康检查时,从46只圈养熊身上收集了血液和蜱虫,以回应之前的血液涂片分析,该分析显示超过一半的居民熊可能患有血液寄生虫。聚合酶链反应在其中一只熊身上检测到一种独特的巴贝斯虫。对困在熊的室外围场外围的蚊子的疾病监测没有发现任何疟疾寄生虫。这项研究标志着婆罗洲马来熊中首次记录到巴贝斯虫和科宁斯伯格氏蜱的病例。需要对媒介的罪证以及巴贝斯虫感染对婆罗洲马来熊健康的影响进行更多的研究。由于巴贝斯虫病的人畜共患性,应采取缓解行动,保护与这些圈养熊或其围栏一起工作或密切接触的任何人员。
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引用次数: 0
Detection of colistin-resistant Escherichia coli isolated from broiler chickens in Kelantan, Malaysia. 马来西亚吉兰丹省肉鸡中耐粘菌素大肠杆菌的检测。
IF 0.8 4区 医学 Q4 PARASITOLOGY Pub Date : 2022-06-01 DOI: 10.47665/tb.39.2.010
S S Devan, E Aklilu, R H Hamdan, M Lemlem, Z Zakaria

Antimicrobial resistant Escherichia coli have become an ever increasing problem in human, and animal health and production. The imprudent use of antibiotics and poor hygienic practices especially in poultry industries have been contributing to the emergence and spread of E. coli species resistant to broad spectrum antibiotics including Colistin. This study was conducted to detect colistin - resistance and antibiotic sensitivity patterns in E. coli isolated from broiler chickens in Kelantan. A total of 320 cloacal swabs were collected from apparently healthy broiler chickens in different districts of Kelantan and were analysed using routine microbiological methods, Kirby-Bauer method for antimicrobial susceptibility test and PCR amplification of species-specific and colistin - resistance encoding genes. Out of the 320 samples, 91 isolates were confirmed as E. coli and 21/91 (23.08%) were positive for colistin - resistant encoding gene, mcr-1. Most of the isolates were resistant to tetracycline (95.24%), chloramphenicol (85.71%), and sulphamethoxazole/ trimethoprim (85.71%). However, the isolates were less resistant towards piperacillin/ tazobactam (4.76%) and meropenem (9.52%). The findings from this study reveal the emerging threats of colistin - resistant in local food animal production, particularly in poultry production industry. However, more comprehensive, and large-scale studies focusing on more resistance patterns using determination of minimum inhibitory concentration (MIC), virulence and resistance characteristics and molecular epidemiology of colistin - resistant E. coli are recommended for better understanding of the epidemiology and to implement the appropriate control and prevention strategies.

耐药大肠杆菌已成为人类和动物健康和生产中日益严重的问题。特别是在家禽业中,不谨慎地使用抗生素和不良的卫生习惯导致了对包括粘菌素在内的广谱抗生素具有耐药性的大肠杆菌物种的出现和传播。本研究旨在检测吉兰丹肉鸡大肠杆菌对粘菌素的耐药性和抗生素敏感性。在吉兰丹不同地区采集表面健康的肉鸡粪拭子320份,采用常规微生物学方法、Kirby-Bauer法进行药敏试验、PCR扩增种特异性和粘菌素抗性编码基因。320份分离物中,91株为大肠杆菌,21/91(23.08%)为耐粘菌素编码基因mcr-1阳性。大多数菌株对四环素(95.24%)、氯霉素(85.71%)和磺胺甲恶唑/甲氧苄啶(85.71%)耐药。但对哌拉西林/他唑巴坦(4.76%)和美罗培南(9.52%)耐药较少。这项研究的结果揭示了当地食用动物生产中出现的耐粘菌素威胁,特别是在家禽生产行业。然而,建议进行更全面、更大规模的研究,重点关注更多的耐药模式,包括测定最低抑制浓度(MIC)、毒力和耐药特征以及耐粘菌素大肠杆菌的分子流行病学,以便更好地了解流行病学并实施适当的控制和预防策略。
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引用次数: 2
Chemical composition and insecticidal activity of Origanum floribundum Munby essential oil endemic plant from Algeria. 阿尔及利亚特有植物鸢尾挥发油的化学成分及杀虫活性。
IF 0.8 4区 医学 Q4 PARASITOLOGY Pub Date : 2022-06-01 DOI: 10.47665/tb.39.2.005
S Mir, O Bouchenak, K Aït Kaci, A Rouane, M Alliliche, K Arab

Among strategies for decreasing diseases, the use of larvicidal plant extracts against mosquito larvae gain an important place in vector control. The aim of the present study was to reveal the insecticidal effectiveness of an endemic medicinal plant on Mosquito-Borne Diseases. The chemical composition of the dried aerial part from Origanum floribundum Essential oil, obtained by hydrodistillation, was characterized by Fourier-transform infrared (FTIR) spectroscopy and gas chromatography-mass spectrometer (GC-MS) system. The potential larvicidal activity of this extract as bioinsecticide was assessed against Culex pipiens. Results showed many functional groups such as phenols and alcohols, besides, the chemical composition by GC-MS identified thymol (86.9%) and p-Cymene (5.1%) as major components. A significant larvicidal effect against the target mosquito species was noted, with values of LC50 at 21.19 mg/l and LC90 at 68.37 mg/l. The results obtained showed that the essential oil of Origanum floribundum with chemotype thymol possess a potent larvicidal activity and could be considered as an eco-friendly alternative for vector control.

在减少疾病的策略中,使用杀幼虫植物提取物来控制蚊子幼虫在病媒控制中占有重要地位。本研究的目的是揭示一种地方性药用植物对蚊媒疾病的杀虫效果。利用傅里叶变换红外光谱(FTIR)和气相色谱-质谱联用(GC-MS)系统对加氢蒸馏法提取的红花精油中风干部分的化学成分进行了表征。评价了该生物杀虫剂对淡色库蚊的潜在杀幼虫活性。经GC-MS鉴定,其主要成分为百里香酚(86.9%)和对伞花烃(5.1%)。对目标蚊种的LC50和LC90分别为21.19 mg/l和68.37 mg/l,具有显著的杀幼虫效果。结果表明,百里香化学型花牛挥发油具有较强的杀幼虫活性,可作为一种生态友好型媒介生物防治方法。
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引用次数: 2
Molecular characterisation of hemagglutinin and neuraminidase genes of the first highly pathogenic Avian Influenza H5N1 2.3.2.1c virus isolated from Sabah, Malaysia. 从马来西亚沙巴分离的首个高致病性H5N1 2.32.1 c禽流感病毒血凝素和神经氨酸酶基因的分子特征
IF 0.8 4区 医学 Q4 PARASITOLOGY Pub Date : 2022-06-01 DOI: 10.47665/tb.39.2.001
B L Leow, S Syamsiah Aini, M Y Faizul Fikri, S Muhammad Redzwan, G H Ong, M S Faizah Hanim

Highly Pathogenic Avian Influenza (HPAI) is a highly contagious disease in poultry. The outbreaks can lead to flock mortality up to 100% in two to three days. In July 2018, high mortality in a commercial layer farm in Kauluan village, Sabah was reported. Samples were sent to Veterinary Research Institute Ipoh for diagnosis. Virus isolation and molecular detection is carried out simultaneously. The causative agent was then identified as AI H5N1 virus by real time reverse transcription-polymerase chain reaction (RT-PCR). The virus was then subjected for further nucleotide sequencing of full length hemagglutinin (HA) and neuraminidase (NA) gene. The PQRERRRKR/GLF motif at the HA cleavage site indicated that the isolate was of HPAI virus. Phylogenetic analysis of the HA gene showed that the isolate was belonged to the clade 2.3.2.1c virus. In the HA gene, besides the S133A substitution, the virus possesses conserved amino acid at most of the avian receptor binding sites including the glutamine (Q) and glycine (G) at position 222 and 224 respectively, indicating that the virus retains the avian-type receptor binding preference. As such, the zoonotic potential of the virus was relatively low. On the other hand, though the N154D and T156A substitution were detected in the same gene, the pandemic potential of this Sabah 2.3.2.1c virus is low in the absence of the Q222L, G224S, H103Y, N220K and T315I. A typical 20 amino acid deletion with loss of four corresponding glycosylation sites in the NA stalk region was visible. Though three NA resistance markers were detected, the virus was predicted to be sensitive to NA inhibitor. This is the first HPAI H5N1 outbreak in Sabah. The introduction of this virus into East Malaysia for the first time raised an alert alarm of the future epidemic potential. Strict farm biosecurity, continuous surveillance programme in poultry, wild birds, migratory birds; molecular epidemiology as well as risk assessment for the virus with pandemic potential are needed in dealing with emergence of new influenza virus in the country.

高致病性禽流感(HPAI)是一种禽类高度传染性疾病。疫情可导致禽群在两到三天内死亡率高达100%。2018年7月,沙巴州Kauluan村的一个商业蛋鸡养殖场报告了高死亡率。样本被送往怡保兽医研究所进行诊断。病毒分离和分子检测同时进行。然后通过实时逆转录聚合酶链反应(RT-PCR)鉴定病原体为H5N1禽流感病毒。然后对病毒进行进一步的全长血凝素(HA)和神经氨酸酶(NA)基因的核苷酸测序。HA裂解位点的PQRERRRKR/GLF基序表明分离物为高致病性禽流感病毒。HA基因的系统发育分析表明该分离物属于2.3.2.1c进化支病毒。在HA基因中,除S133A取代外,病毒在大多数禽类受体结合位点上都有保守的氨基酸,其中谷氨酰胺(Q)和甘氨酸(G)分别位于222位和224位,表明病毒保留了禽类型受体结合偏好。因此,该病毒发生人畜共患的可能性相对较低。另一方面,虽然在同一基因中检测到N154D和T156A的替换,但在缺乏Q222L、G224S、H103Y、N220K和T315I的情况下,该沙巴2.3.2.1c病毒的大流行潜力较低。典型的20个氨基酸缺失和NA茎区4个相应糖基化位点的丢失是可见的。虽然检测到三种NA抗性标记,但预测病毒对NA抑制剂敏感。这是沙巴第一次高致病性H5N1疫情。该病毒首次传入东马来西亚,对未来的流行潜力发出了警报。严格的农场生物安全,持续监测家禽、野鸟、候鸟;在处理该国出现的新流感病毒时,需要对具有大流行潜力的病毒进行分子流行病学和风险评估。
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引用次数: 1
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Tropical biomedicine
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