Pub Date : 2025-04-09DOI: 10.16250/j.32.1915.2024185
H Lu, F Guo, Y Pan, M Peng, L Wu, Y Lin, X Liu, X Yu
<p><strong>Objective: </strong>To investigate the species of ticks in Suizhou City, Hubei Province, so as to provide insights into management of ticks and tick-borne diseases.</p><p><strong>Methods: </strong>During the period between May 2023 and June 2024, livestock breeding farms and vegetation neighboring the place of residence of confirmed and suspected patients with tick-borne disease were selected as sampling points in rural areas from Yindian Township, Gaocheng Township, Wanhe Township, Wushan Township, Xiaolin Township, Xihe Township, Hedian Township and Beijiao Street in Suizhou City, Hubei Province, where confirmed and suspected cases with tick-borne diseases had been reported. The parasitic ticks on the body surface of free-range livestock were captured with tweezers in livestock breeding farms, and free ticks on the vegetation surface were captured with the flagging method. Morphological identification of tick samples was performed under a microscope, and the gender and developmental stage of ticks were determined. One engorged adult tick, 2 to 3 blood-feeding but non-engorged adult ticks, 10 to 15 unfed female ticks, 15 to 20 unfed male ticks, and 30 to 40 tick nymphs or larvae were assigned into a group, respectively. Genomic DNA was extracted from tick samples in each group, and mitochondrial <i>16S rRNA</i> gene was amplified. Sequence analysis was performed with the DNASTAR software, and phylogenetic analysis was performed using the software MEGA 7.0. In addition, the phylogenetic tree was generated using the maximum likelihood method based on the Kimura 2 parameter model.</p><p><strong>Results: </strong>A total of 2 438 ticks were captured from Suizhou City, Hubei Province during the period between May 2023 and June 2024, including 595 free ticks and 1 483 parasitic ticks. Three developmental stages of ticks were captured, including larvae, nymphs, and adults, and 75.18% (1 899/2 438) of captured ticks were adult, in which 79.04% (1 501/1 899) were female. Morphological and molecular biological assays identified one family, three genera and four species of captured ticks, including 2 425 <i>Haemaphysalis longicornis</i> ticks (99.47%) and one <i>H. flava</i> tick (0.04%) of the genus <i>Haemaphysalis</i>, 11 <i>Rhipicephalus microplus</i> ticks (0.45%) of the genus <i>Rhipicephalus</i>, and one <i>Ixodes sinensis</i> tick (0.04%) of the genus <i>Ixodes</i> in the family Ixodidae. Phylogenetic analysis revealed that the <i>H. longicornis</i> sequence (SZ49) in this study was clustered with sequences from Yunnan Province (GenBank accession number: MH024510.1), Hebei Province (GenBank accession number: MK450606.1) and Henan Province (GenBank accession number: MZ230645.1) into a clade, and the <i>H. flava</i> sequence (SZ19) in this study was clustered with sequences from Japan (GenBank accession number: MW064044.1), South Korea (GenBank accession number: ON629585.1), and Jiangsu Province (GenBank accession number: PP494741.1) and H
{"title":"[Investigation of tick species in Suizhou City, Hubei Province from 2023 to 2024].","authors":"H Lu, F Guo, Y Pan, M Peng, L Wu, Y Lin, X Liu, X Yu","doi":"10.16250/j.32.1915.2024185","DOIUrl":"https://doi.org/10.16250/j.32.1915.2024185","url":null,"abstract":"<p><strong>Objective: </strong>To investigate the species of ticks in Suizhou City, Hubei Province, so as to provide insights into management of ticks and tick-borne diseases.</p><p><strong>Methods: </strong>During the period between May 2023 and June 2024, livestock breeding farms and vegetation neighboring the place of residence of confirmed and suspected patients with tick-borne disease were selected as sampling points in rural areas from Yindian Township, Gaocheng Township, Wanhe Township, Wushan Township, Xiaolin Township, Xihe Township, Hedian Township and Beijiao Street in Suizhou City, Hubei Province, where confirmed and suspected cases with tick-borne diseases had been reported. The parasitic ticks on the body surface of free-range livestock were captured with tweezers in livestock breeding farms, and free ticks on the vegetation surface were captured with the flagging method. Morphological identification of tick samples was performed under a microscope, and the gender and developmental stage of ticks were determined. One engorged adult tick, 2 to 3 blood-feeding but non-engorged adult ticks, 10 to 15 unfed female ticks, 15 to 20 unfed male ticks, and 30 to 40 tick nymphs or larvae were assigned into a group, respectively. Genomic DNA was extracted from tick samples in each group, and mitochondrial <i>16S rRNA</i> gene was amplified. Sequence analysis was performed with the DNASTAR software, and phylogenetic analysis was performed using the software MEGA 7.0. In addition, the phylogenetic tree was generated using the maximum likelihood method based on the Kimura 2 parameter model.</p><p><strong>Results: </strong>A total of 2 438 ticks were captured from Suizhou City, Hubei Province during the period between May 2023 and June 2024, including 595 free ticks and 1 483 parasitic ticks. Three developmental stages of ticks were captured, including larvae, nymphs, and adults, and 75.18% (1 899/2 438) of captured ticks were adult, in which 79.04% (1 501/1 899) were female. Morphological and molecular biological assays identified one family, three genera and four species of captured ticks, including 2 425 <i>Haemaphysalis longicornis</i> ticks (99.47%) and one <i>H. flava</i> tick (0.04%) of the genus <i>Haemaphysalis</i>, 11 <i>Rhipicephalus microplus</i> ticks (0.45%) of the genus <i>Rhipicephalus</i>, and one <i>Ixodes sinensis</i> tick (0.04%) of the genus <i>Ixodes</i> in the family Ixodidae. Phylogenetic analysis revealed that the <i>H. longicornis</i> sequence (SZ49) in this study was clustered with sequences from Yunnan Province (GenBank accession number: MH024510.1), Hebei Province (GenBank accession number: MK450606.1) and Henan Province (GenBank accession number: MZ230645.1) into a clade, and the <i>H. flava</i> sequence (SZ19) in this study was clustered with sequences from Japan (GenBank accession number: MW064044.1), South Korea (GenBank accession number: ON629585.1), and Jiangsu Province (GenBank accession number: PP494741.1) and H","PeriodicalId":38874,"journal":{"name":"中国血吸虫病防治杂志","volume":"37 2","pages":"184-189"},"PeriodicalIF":0.0,"publicationDate":"2025-04-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144162776","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-04-08DOI: 10.16250/j.32.1915.2025018
J Xu, S Li, Q Li, S Guo, S Li, X Zhou
Schistosomiasis is prevalent in 78 countries and territories worldwide, while the eastern and western parts of sub-Sahara Africa bear the highest disease burden due to schistosomiasis. Recently, climate change, international trade and travel, urbanization and war have increased the risk of cross-boundary importation and transmission of schistosomiasis, and schistosomiasis has increasingly become a public health concern in non-endemic countries and territories. Biomphalaria straminea, the intermediate host of Schistosoma mansoni, has colonized in southern China and its habitats continue to move northward. In addition, cross-boundary imported cases of schistosomiasis have been reported occasionally in China. However, the real number of cases may be underestimated greatly due to insufficient diagnostic capacity and weak awareness of case reporting for overseas imported schistosomiasis in healthcare facilities. It is necessary to establish a multi-party collaborative mechanism, improve corresponding systems and technical specifications, reinforce surveillance and early warning, and border management, enhance technical reserves and capability building, and improve the awareness of schistosomiasis prevention and healthcare-seeking among entry-exit personnel, in order to effectively address the threat of cross-boundary imported schistosomiasis.
{"title":"[Strategic thinking on management of cross-boundary imported schistosomiasis].","authors":"J Xu, S Li, Q Li, S Guo, S Li, X Zhou","doi":"10.16250/j.32.1915.2025018","DOIUrl":"https://doi.org/10.16250/j.32.1915.2025018","url":null,"abstract":"<p><p>Schistosomiasis is prevalent in 78 countries and territories worldwide, while the eastern and western parts of sub-Sahara Africa bear the highest disease burden due to schistosomiasis. Recently, climate change, international trade and travel, urbanization and war have increased the risk of cross-boundary importation and transmission of schistosomiasis, and schistosomiasis has increasingly become a public health concern in non-endemic countries and territories. Biomphalaria straminea, the intermediate host of Schistosoma mansoni, has colonized in southern China and its habitats continue to move northward. In addition, cross-boundary imported cases of schistosomiasis have been reported occasionally in China. However, the real number of cases may be underestimated greatly due to insufficient diagnostic capacity and weak awareness of case reporting for overseas imported schistosomiasis in healthcare facilities. It is necessary to establish a multi-party collaborative mechanism, improve corresponding systems and technical specifications, reinforce surveillance and early warning, and border management, enhance technical reserves and capability building, and improve the awareness of schistosomiasis prevention and healthcare-seeking among entry-exit personnel, in order to effectively address the threat of cross-boundary imported schistosomiasis.</p>","PeriodicalId":38874,"journal":{"name":"中国血吸虫病防治杂志","volume":"37 2","pages":"107-111"},"PeriodicalIF":0.0,"publicationDate":"2025-04-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144162734","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-03-25DOI: 10.16250/j.32.1915.2024147
Y Bai, W Li, W Luo, Y Yu, D Li, J Zhao, L He
Avian coccidiosis, an acute parasitic disease that mainly harms chicks, is widely prevalent across the world, which poses a serious threat to poultry industry. Because of the single prophylactic formulations, veterinary clinical treatment of coccidiosis mainly relies on chemically synthesized agents, polyether ionophores and Chinese herbal medicines. The introduction of novel anticoccidial drugs is slow for a long period of time, and there is an increasing problem of anticoccidial drug resistance following long-term use, which has become an urgent problem to be solved in poultry industry. This review summarizes the levels of anticoccidial drug resistance across China from 2018 to 2023, and analyzes the resistance to various anticoccidial agents in coccidia. It is indicated that the overall prevalence of anticoccidial drug resistance is high in coccidia, and development of novel anticoccidial agents and products with reduced antibiotics use and alternatives of antibiotics is of an urgent need.
{"title":"[Current status of anticoccidial drug resistance in China].","authors":"Y Bai, W Li, W Luo, Y Yu, D Li, J Zhao, L He","doi":"10.16250/j.32.1915.2024147","DOIUrl":"https://doi.org/10.16250/j.32.1915.2024147","url":null,"abstract":"<p><p>Avian coccidiosis, an acute parasitic disease that mainly harms chicks, is widely prevalent across the world, which poses a serious threat to poultry industry. Because of the single prophylactic formulations, veterinary clinical treatment of coccidiosis mainly relies on chemically synthesized agents, polyether ionophores and Chinese herbal medicines. The introduction of novel anticoccidial drugs is slow for a long period of time, and there is an increasing problem of anticoccidial drug resistance following long-term use, which has become an urgent problem to be solved in poultry industry. This review summarizes the levels of anticoccidial drug resistance across China from 2018 to 2023, and analyzes the resistance to various anticoccidial agents in coccidia. It is indicated that the overall prevalence of anticoccidial drug resistance is high in coccidia, and development of novel anticoccidial agents and products with reduced antibiotics use and alternatives of antibiotics is of an urgent need.</p>","PeriodicalId":38874,"journal":{"name":"中国血吸虫病防治杂志","volume":"37 2","pages":"217-222"},"PeriodicalIF":0.0,"publicationDate":"2025-03-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144162757","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-03-21DOI: 10.16250/j.32.1915.2024229
L Chen, H Luo, C Wu, J Wan, J Wu, H Liu, B Li, S Yang
<p><strong>Objective: </strong>To evaluate the effectiveness of an artificial intelligence (AI)-enabled microscopic imaging recognition system integrated in the modified Kato-Katz thick smear technique for detection of <i>Schistosoma japonicum</i> eggs, so as to provide insights into precise control and elimination of schistosomiasis.</p><p><strong>Methods: </strong>In October 2023, 20 fecal samples were collected from healthy residents negative for <i>S. japonicum</i> infection in Wuhan City, and each fecal sample was prepared into 4 Kato-Katz test slides, with 3 slides added <i>S. japonicum</i> egg suspensions with concentrations of approximately 25, 10, and 5 eggs per 10 μL, respectively, and one untreated. A total of 80 Kato-Katz test slides were prepared, and were divided into mild, moderate, and severe infection groups, and a negative control group, according to the number of eggs per gram of feces on each slide, with 20 slides in each group. <i>S. japonicum</i> eggs were detected on 80 Kato-Katz test slides with the AI-enabled microscopic imaging recognition system and manual microscopy, and the differences were compared between the two methods in terms of average detection time, accurate rate of qualitative detection, accurate rate of quantitative detection, percentage of missed detection, and percentage of false detection.</p><p><strong>Results: </strong>The average detection time of the imaging recognition system was longer than manual microscopy for detection of <i>S. japonicum</i> eggs on Kato-Katz test slides in all groups [(16.70 ± 0.01) min vs. (15.78 ± 2.11) min; <i>t</i> = 3.90, <i>P</i> <0.05]. The detection time of the imaging recognition system was shorter than manual microscopy for detection of <i>S. japonicum</i> eggs on Kato-Katz test slides in the severe infection group (<i>t</i> = -3.91, <i>P</i> < 0.05), but was longer than manual microscopy in the the mild infection group (<i>t</i> = 5.03, <i>P</i> < 0.05) and the negative control group (<i>t</i> = 8.37, <i>P</i> < 0.05), while there was no significant difference in the detection time between the two methods in the moderate infection group (<i>t</i> = -0.09, <i>P</i> > 0.05). In addition, the imaging recognition system [97.50% (78/80) and 91.67% (55/60)] had higher accurate rates of both qualitative and quantitative detections than manual microscopy [81.25% (65/80) and 31.67% (19/60)] (χ<sup>2</sup> = 11.08 and 34.11, both <i>P</i> values < 0.05), and the imaging recognition system had a lower percentage of missed detection in the infection groups [3.33% (2/60)] and a lower percentage of false detection in the negative control group (0) than manual microscopy [13.33% (8/60) and 35.00% (7/20)] (χ<sup>2</sup> = 6.07, 5.14, both <i>P</i> values < 0.05).</p><p><strong>Conclusions: </strong>The AI-enabled microscopic imaging recognition system is effective to improve the accuracy for detection of <i>S. japonicum</i> eggs with the Kato-Katz technique, and is accurate to quant
目的:评价将人工智能(AI)显微成像识别系统集成到改良加藤-卡茨厚涂片技术中检测日本血吸虫虫卵的有效性,为血吸虫病的精准控制和消除提供依据。方法:于2023年10月在武汉市采集日本血吸虫感染阴性健康居民粪便标本20份,将每份粪便标本制成4个加托卡兹试验载玻片,其中3个载玻片分别添加浓度约为25、10和5个/ 10 μL的日本血吸虫卵悬液,1个未处理。共制备80张加托-卡茨试验载玻片,根据每张载玻片上每克粪便的卵数分为轻度、中度、重度感染组和阴性对照组,每组20张载玻片。采用人工智能显微镜成像识别系统和人工显微镜对80张Kato-Katz玻片上的日本血吸虫卵进行检测,比较两种方法在平均检测时间、定性检测正确率、定量检测正确率、漏检率、误检率等方面的差异。结果:成像识别系统对加藤-卡茨载玻片上日本血吸虫卵的平均检测时间均长于人工显微镜检测时间[(16.70±0.01)min vs(15.78±2.11)min];t = 3.90,重症感染组(t = -3.91, P < 0.05),轻度感染组(t = 5.03, P < 0.05)和阴性对照组(t = 8.37, P < 0.05)较手工镜检法检测日本血吸虫卵时间长,中度感染组(t = -0.09, P < 0.05)两种方法检测时间差异无统计学意义。影像识别系统定性和定量检出率分别为97.50%(78/80)和91.67%(55/60),均高于人工镜检系统定性和定量检出率分别为81.25%(65/80)和31.67% (19/60)(χ2 = 11.08、34.11,P值均< 0.05);影像识别系统感染组的漏检率[3.33%(2/60)]低于人工镜检组[13.33%(8/60)和35.00%(7/20)],阴性对照组的误检率(0)低于人工镜检组[χ2 = 6.07, 5.14, P值均< 0.05]。结论:人工智能显微镜成像识别系统可有效提高加藤-卡茨技术检测日本血吸虫虫卵的准确性,且定量准确、操作简单,可为血吸虫病等寄生虫病的诊断提供技术支持。
{"title":"[Effectiveness of an artificial intelligence-enabled microscopic imaging recognition system for detection of <i>Schistosoma japonicum</i> eggs].","authors":"L Chen, H Luo, C Wu, J Wan, J Wu, H Liu, B Li, S Yang","doi":"10.16250/j.32.1915.2024229","DOIUrl":"https://doi.org/10.16250/j.32.1915.2024229","url":null,"abstract":"<p><strong>Objective: </strong>To evaluate the effectiveness of an artificial intelligence (AI)-enabled microscopic imaging recognition system integrated in the modified Kato-Katz thick smear technique for detection of <i>Schistosoma japonicum</i> eggs, so as to provide insights into precise control and elimination of schistosomiasis.</p><p><strong>Methods: </strong>In October 2023, 20 fecal samples were collected from healthy residents negative for <i>S. japonicum</i> infection in Wuhan City, and each fecal sample was prepared into 4 Kato-Katz test slides, with 3 slides added <i>S. japonicum</i> egg suspensions with concentrations of approximately 25, 10, and 5 eggs per 10 μL, respectively, and one untreated. A total of 80 Kato-Katz test slides were prepared, and were divided into mild, moderate, and severe infection groups, and a negative control group, according to the number of eggs per gram of feces on each slide, with 20 slides in each group. <i>S. japonicum</i> eggs were detected on 80 Kato-Katz test slides with the AI-enabled microscopic imaging recognition system and manual microscopy, and the differences were compared between the two methods in terms of average detection time, accurate rate of qualitative detection, accurate rate of quantitative detection, percentage of missed detection, and percentage of false detection.</p><p><strong>Results: </strong>The average detection time of the imaging recognition system was longer than manual microscopy for detection of <i>S. japonicum</i> eggs on Kato-Katz test slides in all groups [(16.70 ± 0.01) min vs. (15.78 ± 2.11) min; <i>t</i> = 3.90, <i>P</i> <0.05]. The detection time of the imaging recognition system was shorter than manual microscopy for detection of <i>S. japonicum</i> eggs on Kato-Katz test slides in the severe infection group (<i>t</i> = -3.91, <i>P</i> < 0.05), but was longer than manual microscopy in the the mild infection group (<i>t</i> = 5.03, <i>P</i> < 0.05) and the negative control group (<i>t</i> = 8.37, <i>P</i> < 0.05), while there was no significant difference in the detection time between the two methods in the moderate infection group (<i>t</i> = -0.09, <i>P</i> > 0.05). In addition, the imaging recognition system [97.50% (78/80) and 91.67% (55/60)] had higher accurate rates of both qualitative and quantitative detections than manual microscopy [81.25% (65/80) and 31.67% (19/60)] (χ<sup>2</sup> = 11.08 and 34.11, both <i>P</i> values < 0.05), and the imaging recognition system had a lower percentage of missed detection in the infection groups [3.33% (2/60)] and a lower percentage of false detection in the negative control group (0) than manual microscopy [13.33% (8/60) and 35.00% (7/20)] (χ<sup>2</sup> = 6.07, 5.14, both <i>P</i> values < 0.05).</p><p><strong>Conclusions: </strong>The AI-enabled microscopic imaging recognition system is effective to improve the accuracy for detection of <i>S. japonicum</i> eggs with the Kato-Katz technique, and is accurate to quant","PeriodicalId":38874,"journal":{"name":"中国血吸虫病防治杂志","volume":"37 4","pages":"415-419"},"PeriodicalIF":0.0,"publicationDate":"2025-03-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145410359","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-03-21DOI: 10.16250/j.32.1915.2024200
S Wang, H Luo, Y Li, H Wang, C Liu, Y Xiong, J Zhang, W Zhu
Objective: To evaluate the effectiveness of the integrated schistosomiasis control programme in Wuhan City from 2005 to 2023, so as to provide insights into precision control and elimination of schistosomiasis.
Methods: The integrated measures for schistosomiasis control implemented by health, agriculture, water resources, and forestry departments of Wuhan City, and the epidemiological data of schistosomiasis in Wuhan City were collected from 2005 to 2023, and the prevalence of human schistosomiasis, prevalence of Schistosoma japonicum infections in humans and bovines, areas of S. japonicum-infected snail habitats, areas of snail habitats in inner embankments, and actual areas of snail habitats were retrieved. In addition, the trends in prevalence of schistosomiasis in humans and livestock and snail status were evaluated in Wuhan City from 2005 to 2023 using Mann-Kendall test and a Joinpoint regression model.
Results: Mann-Kendall test revealed a tendency towards a decline in the prevalence of human schistosomiasis (Z = -4.41, P < 0.01), prevalence of S. japonicum infections in humans (Z = -4.89, P < 0.01) and bovines (Z = -4.50, P < 0.01), areas of S. japonicum-infected snail habitats (Z = -3.91, P < 0.01), areas of snail habitats in inner embankments (Z = -2.28, P = 0.02), and actual areas of snail habitats (Z = -5.95, P < 0.01) in Wuhan City from 2005 to 2023. Joinpoint regression analysis showed an average annual reduction of 8.58% in the prevalence of human schistosomiasis in Wuhan City from 2005 to 2023 [average annual percent change (AAPC) = -8.58%, 95% confidence interval (CI): (-10.02%, -6.65%), P < 0.01], with two joinpoints in 2013 and 2016, respectively, and the tendency towards a decline showed statistical significance during the period from 2013 through 2016 [annual percent change (APC) = -34.41%, 95% CI: (-40.36%, -20.01%), P < 0.01]. The prevalence of S. japonicum human infections appeared an average annual reduction of 51.91% in Wuhan City from 2005 to 2023 [AAPC = -51.91%, 95% CI: (-58.12%, -44.25%), P < 0.01], with two joinpoints in 2014 and 2017, respectively, and the tendency towards a decline showed statistical significance during the period from 2014 through 2017 [APC = -98.17%, 95% CI: (-99.17%, -90.87%), P < 0.01]. The prevalence of S. japonicum infections in bovines appeared an average annual reduction of 53.12% in Wuhan City from 2005 to 2023 [AAPC = -53.12%, 95% CI: (-59.65%, -42.44%), P < 0.01], with two joinpoints in 2011 and 2014, respectively, and the tendency towards a decline showed statistical significance during the period from 2014 through 2017 [APC = -98.63%, 95% CI: (-99.44%, -90.93%), P < 0.01]. The areas of S. japonicum-infected
目的:评价武汉市2005 - 2023年血吸虫病综合防治规划的效果,为精准控制和消灭血吸虫病提供依据。方法:收集武汉市卫生、农业、水利、林业等部门2005 - 2023年血吸虫病综合防治措施和武汉市血吸虫病流行病学资料,检索2005 - 2023年武汉市人血吸虫病流行情况、人、牛血吸虫病流行情况、血吸虫病钉螺感染分布区、河堤内钉螺分布区和实际钉螺分布区。利用Mann-Kendall检验和联合点回归模型分析了武汉市2005 - 2023年人、牲畜血吸虫病流行趋势和血吸虫病钉螺状况。结果:Mann-Kendall测试显示一个下降的趋势,人类血吸虫病的患病率(Z = -4.41, P < 0.01), s .日本血吸虫感染的患病率在人类(Z = -4.89, P < 0.01)和牛(Z = -4.50, P < 0.01), s领域japonicum-infected蜗牛栖息地(Z = -3.91, P < 0.01),地区的蜗牛栖息地内堤防(Z = -2.28, P = 0.02),和实际领域的蜗牛栖息地(Z = -5.95, P < 0.01)从2005年到2023年在武汉城市。联合点回归分析显示,2005 - 2023年武汉市人血吸虫病患病率年均下降8.58%[年均百分率变化(AAPC) = -8.58%, 95%可信区间(CI): (-10.02%, -6.65%), P < 0.01],其中2013年和2016年分别有两个联合点,2013 - 2016年呈下降趋势[年百分率变化(APC) = -34.41%, 95% CI: (-40.36%, -20.01%), P < 0.01]。武汉市2005 - 2023年日本血吸虫人感染流行率年均下降51.91% [AAPC = -51.91%, 95% CI: (-58.12%, -44.25%), P < 0.01],其中2014 - 2017年有2个接点,呈下降趋势,具有统计学意义[APC = -98.17%, 95% CI: (-99.17%, -90.87%), P < 0.01]。2005 - 2023年,武汉市牛日本血吸虫感染率年均下降53.12% [AAPC = -53.12%, 95% CI: (-59.65%, -42.44%), P < 0.01],其中2011年和2014年有2个接点,2014 - 2017年呈下降趋势,差异有统计学意义[APC = -98.63%, 95% CI: (-99.44%, -90.93%), P < 0.01]。2005 - 2023年,武汉市血吸虫感染的蜗牛栖息地面积年均减少47.09% [AAPC = -47.09%, 95% CI: (-52.92%, -38.26%), P < 0.01],其中2011 - 2014年有2个接合点,下降趋势具有统计学意义[APC = -97.27%, 95% CI: (-98.65%, -88.06%), P < 0.01]。2005 - 2023年,武汉市河堤内螺生境面积年均减少4.45% [AAPC = -4.45%, 95% CI: (-5.18%, -3.82%), P < 0.01],其中2011年、2015年和2018年为3个节点,2005 - 2011年呈下降趋势,且有统计学意义[APC = -16.38%, 95% CI: (-20.15%, -14.25%), P < 0.01]。2005 - 2023年,武汉市实际蜗牛栖息地面积年均减少2.65% [AAPC = -2.65%, 95% CI: (-2.89%, -2.40%), P < 0.01], 2013 - 2023年出现拐点,下降趋势具有统计学意义[APC = -4.06%, 95% CI: (-4.66%, -3.58%), P < 0.01]。结论:2005 - 2023年武汉市血吸虫病综合防治取得了显著效果,由于人、畜血吸虫病和钉螺状况,该病发病率呈下降趋势。继续实施以日本血吸虫感染源管理为重点的血吸虫病综合防治策略,巩固血吸虫病防治成果,实现全市消除血吸虫病的目标。
{"title":"[Effectiveness of the integrated schistosomiasis control programme in Wuhan City from 2005 to 2023].","authors":"S Wang, H Luo, Y Li, H Wang, C Liu, Y Xiong, J Zhang, W Zhu","doi":"10.16250/j.32.1915.2024200","DOIUrl":"https://doi.org/10.16250/j.32.1915.2024200","url":null,"abstract":"<p><strong>Objective: </strong>To evaluate the effectiveness of the integrated schistosomiasis control programme in Wuhan City from 2005 to 2023, so as to provide insights into precision control and elimination of schistosomiasis.</p><p><strong>Methods: </strong>The integrated measures for schistosomiasis control implemented by health, agriculture, water resources, and forestry departments of Wuhan City, and the epidemiological data of schistosomiasis in Wuhan City were collected from 2005 to 2023, and the prevalence of human schistosomiasis, prevalence of <i>Schistosoma japonicum</i> infections in humans and bovines, areas of <i>S. japonicum</i>-infected snail habitats, areas of snail habitats in inner embankments, and actual areas of snail habitats were retrieved. In addition, the trends in prevalence of schistosomiasis in humans and livestock and snail status were evaluated in Wuhan City from 2005 to 2023 using Mann-Kendall test and a Joinpoint regression model.</p><p><strong>Results: </strong>Mann-Kendall test revealed a tendency towards a decline in the prevalence of human schistosomiasis (<i>Z</i> = -4.41, <i>P</i> < 0.01), prevalence of <i>S. japonicum</i> infections in humans (<i>Z</i> = -4.89, <i>P</i> < 0.01) and bovines (<i>Z</i> = -4.50, <i>P</i> < 0.01), areas of <i>S. japonicum</i>-infected snail habitats (<i>Z</i> = -3.91, <i>P</i> < 0.01), areas of snail habitats in inner embankments (<i>Z</i> = -2.28, <i>P</i> = 0.02), and actual areas of snail habitats (<i>Z</i> = -5.95, <i>P</i> < 0.01) in Wuhan City from 2005 to 2023. Joinpoint regression analysis showed an average annual reduction of 8.58% in the prevalence of human schistosomiasis in Wuhan City from 2005 to 2023 [average annual percent change (AAPC) = -8.58%, 95% confidence interval (<i>CI</i>): (-10.02%, -6.65%), <i>P</i> < 0.01], with two joinpoints in 2013 and 2016, respectively, and the tendency towards a decline showed statistical significance during the period from 2013 through 2016 [annual percent change (APC) = -34.41%, 95% <i>CI</i>: (-40.36%, -20.01%), <i>P</i> < 0.01]. The prevalence of <i>S. japonicum</i> human infections appeared an average annual reduction of 51.91% in Wuhan City from 2005 to 2023 [AAPC = -51.91%, 95% <i>CI</i>: (-58.12%, -44.25%), <i>P</i> < 0.01], with two joinpoints in 2014 and 2017, respectively, and the tendency towards a decline showed statistical significance during the period from 2014 through 2017 [APC = -98.17%, 95% <i>CI</i>: (-99.17%, -90.87%), <i>P</i> < 0.01]. The prevalence of <i>S. japonicum</i> infections in bovines appeared an average annual reduction of 53.12% in Wuhan City from 2005 to 2023 [AAPC = -53.12%, 95% <i>CI</i>: (-59.65%, -42.44%), <i>P</i> < 0.01], with two joinpoints in 2011 and 2014, respectively, and the tendency towards a decline showed statistical significance during the period from 2014 through 2017 [APC = -98.63%, 95% <i>CI</i>: (-99.44%, -90.93%), <i>P</i> < 0.01]. The areas of <i>S. japonicum</i>-infected","PeriodicalId":38874,"journal":{"name":"中国血吸虫病防治杂志","volume":"37 2","pages":"176-183"},"PeriodicalIF":0.0,"publicationDate":"2025-03-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144162773","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-03-18DOI: 10.16250/j.32.1915.2025044
Y Yang, Q Wang, L Xiang, Y Meng, C Zhang, J Fu
Objective: To investigate the seroprevalence of antibody against Toxoplasma gondii among patients with hematological malignancies, and compare it with that among health individuals, so as to provide insights into unraveling the pathogenesis of hematological malignancies.
Methods: A total of 225 patients with hematological malignancies in Department of Hematology, Xuzhou Central Hospital and 300 healthy individuals in the same hospital were enrolled from 2017 to 2024. Blood samples were collected from all subjects, and the serum IgG and IgM antibodies against T. gondii were detected using chemiluminescent immunoassay. Demographic and clinical features were collected from patients with hematological malignancies, including gender, age, contact with cats, consumption of raw or undercooked meat, type of malignancy, clinical symptoms, blood transfusion and treatment, and the seroprevalence of anti-T. gondii antibody was compared among patients with different characteristics.
Results: The age (t = 0.72, P > 0.05) and gender (χ2 = 0.93, P > 0.05) were compared between patients with hematological malignancies and healthy individuals. The seroprevalence of T. gondii infection was 20.89% among patients with hematological malignancies and 4.33% among healthy individuals (χ2 = 34.81, P < 0.01), and the seroprevalence of anti-T. gondii IgG antibody was 20.89% among patients with hematological malignancies and 4.33% among healthy individuals (χ2 = 34.81, P < 0.01), while there was no significant difference in the seroprevalence of anti-T. gondii IgM antibody between patients with hematological malignancies and healthy individuals (1.33% vs. 0; corrected χ2 = 2.02, P > 0.05). The seroprevalence of T. gondii infection was 23.08% among patients with leukemia, 16.67% among patients with lymphoma, 19.23% among patients with multiple myeloma, 24.00% among patients with myeloproliferative neoplasm, and 26.09% among patients with myelodysplastic syndrome (χ2 = 1.44, P > 0.05), and was all higher than among healthy individuals (corrected χ2 = 23.92, 10.74, 13.76, 12.84 and 14.54; all P values < 0.01). In addition, there were no significant differences in the detection of anti-T. gondii antibody among patients with hematological malignancies in terms of gender, age, contact with cats, consumption of raw or undercooked meat, chemotherapy or blood transfusion (χ2 = 0.76, 1.97, 0, 2.81, 2.38 and 0.66; all P values > 0.05).
Conclusions: There is a high risk of T. gondii infection among patients with hematological malignancies, and intensified surveillance of T. gondii infection is recommended among patients with hematological malignancies.
目的:了解恶性血液病患者血清刚地弓形虫抗体的阳性率,并与健康人群进行比较,为揭示恶性血液病的发病机制提供依据。方法:选取2017 - 2024年徐州市中心医院血液科恶性血液病患者225例和该医院健康人群300例。采集所有受试者血样,采用化学发光免疫法检测血清中抗弓形虫IgG和IgM抗体。收集血液学恶性肿瘤患者的人口统计学和临床特征,包括性别、年龄、与猫的接触、食用生肉或未煮熟的肉、恶性肿瘤类型、临床症状、输血和治疗,以及抗t抗体的血清阳性率。比较不同特征患者的弓形虫抗体。结果:血液病患者与健康人的年龄(t = 0.72, P < 0.05)、性别(χ2 = 0.93, P < 0.05)差异有统计学意义。血液系统恶性肿瘤患者弓形虫感染的血清阳性率为20.89%,健康人群为4.33% (χ2 = 34.81, P < 0.01);恶性血液病患者弓形虫IgG抗体阳性率为20.89%,健康人为4.33% (χ2 = 34.81, P < 0.01),血清抗t抗体阳性率差异无统计学意义。恶性血液病患者与健康人群间弓形虫IgM抗体阳性率(1.33% vs. 0;χ2 = 2.02, P < 0.05)。血清弓形虫感染阳性率在白血病、淋巴瘤、多发性骨髓瘤、骨髓增生性肿瘤和骨髓增生异常综合征患者中分别为23.08%、16.67%、19.23%、24.00%和26.09% (χ2 = 1.44, P < 0.05),均高于健康人群(χ2校正后分别为23.92、10.74、13.76、12.84、14.54;P值均< 0.01)。此外,两组在抗t抗体检测上也无显著差异。恶性血液病患者的性别、年龄、与猫接触、食用生肉或未煮熟的肉、化疗或输血的弓形虫抗体水平(χ2 = 0.76、1.97、0、2.81、2.38、0.66;P值均为> 0.05)。结论:血液系统恶性肿瘤患者中弓形虫感染的风险较高,建议加强对血液系统恶性肿瘤患者弓形虫感染的监测。
{"title":"[Seroprevalence of antibody against <i>Toxoplasma gondii</i> among patients with hematological malignancies].","authors":"Y Yang, Q Wang, L Xiang, Y Meng, C Zhang, J Fu","doi":"10.16250/j.32.1915.2025044","DOIUrl":"https://doi.org/10.16250/j.32.1915.2025044","url":null,"abstract":"<p><strong>Objective: </strong>To investigate the seroprevalence of antibody against <i>Toxoplasma gondii</i> among patients with hematological malignancies, and compare it with that among health individuals, so as to provide insights into unraveling the pathogenesis of hematological malignancies.</p><p><strong>Methods: </strong>A total of 225 patients with hematological malignancies in Department of Hematology, Xuzhou Central Hospital and 300 healthy individuals in the same hospital were enrolled from 2017 to 2024. Blood samples were collected from all subjects, and the serum IgG and IgM antibodies against <i>T. gondii</i> were detected using chemiluminescent immunoassay. Demographic and clinical features were collected from patients with hematological malignancies, including gender, age, contact with cats, consumption of raw or undercooked meat, type of malignancy, clinical symptoms, blood transfusion and treatment, and the seroprevalence of anti-<i>T. gondii</i> antibody was compared among patients with different characteristics.</p><p><strong>Results: </strong>The age (<i>t</i> = 0.72, <i>P</i> > 0.05) and gender (χ<sup>2</sup> = 0.93, <i>P</i> > 0.05) were compared between patients with hematological malignancies and healthy individuals. The seroprevalence of <i>T. gondii</i> infection was 20.89% among patients with hematological malignancies and 4.33% among healthy individuals (χ<sup>2</sup> = 34.81, <i>P</i> < 0.01), and the seroprevalence of anti-<i>T. gondii</i> IgG antibody was 20.89% among patients with hematological malignancies and 4.33% among healthy individuals (χ<sup>2</sup> = 34.81, <i>P</i> < 0.01), while there was no significant difference in the seroprevalence of anti-<i>T. gondii</i> IgM antibody between patients with hematological malignancies and healthy individuals (1.33% vs. 0; corrected χ<sup>2</sup> = 2.02, <i>P</i> > 0.05). The seroprevalence of <i>T. gondii</i> infection was 23.08% among patients with leukemia, 16.67% among patients with lymphoma, 19.23% among patients with multiple myeloma, 24.00% among patients with myeloproliferative neoplasm, and 26.09% among patients with myelodysplastic syndrome (χ<sup>2</sup> = 1.44, <i>P</i> > 0.05), and was all higher than among healthy individuals (corrected χ<sup>2</sup> = 23.92, 10.74, 13.76, 12.84 and 14.54; all <i>P</i> values < 0.01). In addition, there were no significant differences in the detection of anti-<i>T. gondii</i> antibody among patients with hematological malignancies in terms of gender, age, contact with cats, consumption of raw or undercooked meat, chemotherapy or blood transfusion (χ<sup>2</sup> = 0.76, 1.97, 0, 2.81, 2.38 and 0.66; all <i>P</i> values > 0.05).</p><p><strong>Conclusions: </strong>There is a high risk of <i>T. gondii</i> infection among patients with hematological malignancies, and intensified surveillance of <i>T. gondii</i> infection is recommended among patients with hematological malignancies.</p>","PeriodicalId":38874,"journal":{"name":"中国血吸虫病防治杂志","volume":"37 1","pages":"93-97"},"PeriodicalIF":0.0,"publicationDate":"2025-03-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144040387","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-03-18DOI: 10.16250/j.32.1915.2024199
J Li, T Dang, Z Zhao
<p><strong>Objective: </strong>To investigate the effects of <i>Toxoplasma gondii</i> type I and II rhoptry protein 16 (ROP16) on the polarization and inflammatory response of mouse alveolar macrophages, so as to provide the scientific evidence for unveiling the immunoregulatory mechanisms following <i>T. gondii</i> infection in host cells and the clinical diagnosis and treatment of pulmonary toxoplasmosis.</p><p><strong>Methods: </strong>Mouse alveolar macrophages served as blank controls, and mouse alveolar macrophages transfected with the empty lentiviral expression vector served as negative controls, and mouse alveolar macrophages transfected with lentiviral vectors overexpressing <i>T. gondii</i> type I and II ROP16 served as the type I and II ROP16 overexpression groups. Following puromycin selection, stably transfected cells that overexpressed type I and II ROP16 were generated, observed for green fluorescence expression under a fluorescence microscope and verified using PCR, Western blotting and real-time quantitative reverse transcription PCR (RT-qPCR) assays. The expression of ROP16, inducible nitric oxide synthase (iNOS), arginase (Arg)-1, mannose receptor (CD206), cluster of differentiation 86 (CD86), NOD-like receptor thermal protein domain associated protein 3 (NLRP3), caspase-1, apoptosis-associated speck-like protein containing a CARD (ASC), and interleukin (IL)-1β proteins was determined in mouse alveolar macrophages using Western blotting assay, and the mRNA levels of <i>ROP16</i>, <i>iNOS</i>, <i>IL-1β</i>, <i>IL-4</i>, <i>IL-12</i>, <i>IL-18</i>, <i>Arg-1</i>, <i>IL-10</i>, <i>IL-6</i>, tumor necrosis factor (<i>TNF</i>)-<i>α</i> and transforming growth factor (<i>TGF</i>)-<i>β</i> were detected in mouse alveolar macrophages using RT-qPCR assay.</p><p><strong>Results: </strong>Fluorescence microscopy showed 90% of mouse alveolar macrophages producing green fluorescent signals in the type Iand II ROP16 overexpression groups and the negative control group. The relative ROP16 protein expression was 1.000 ± 0.000, 1.003 ± 0.020, 1.349 ± 0.055, and 1.376 ± 0.080 in mouse alveolar macrophages in the blank control group, negative control group, and type Iand IIROP16 overexpression groups (<i>F</i> = 35.30, <i>P</i> < 0.01), and the relative <i>ROP16 mRNA</i> expression was 1.007 ± 0.172, 2.030 ± 0.356, 1 409.579 ± 75.960, and 1 413.581 ± 27.712 in the blank control group, negative control group, and type Iand II ROP16 overexpression groups (<i>F</i> = 811.00, <i>P</i> < 0.01). The ROP16 expression was significantly higher in the type Iand IIROP16 overexpression groups than in the blank control group at both protein and mRNA levels (all <i>P</i> value < 0.01). Western blotting assay detected significant differences among the four groups in terms of iNOS, Arg-1, CD86, CD206, NLRP3, caspase-1, ASC, and IL-1β protein expression (<i>F</i> = 124.70, 82.40, 79.82, 919.40, 84.74, 39.85, 2 354.00 and 65.96, all <i>P</i> values < 0.05), and th
{"title":"[Effects of <i>Toxoplasma gondii</i> type I/II rhoptry protein 16 on the polarization and inflammatory response of mouse alveolar macrophages].","authors":"J Li, T Dang, Z Zhao","doi":"10.16250/j.32.1915.2024199","DOIUrl":"https://doi.org/10.16250/j.32.1915.2024199","url":null,"abstract":"<p><strong>Objective: </strong>To investigate the effects of <i>Toxoplasma gondii</i> type I and II rhoptry protein 16 (ROP16) on the polarization and inflammatory response of mouse alveolar macrophages, so as to provide the scientific evidence for unveiling the immunoregulatory mechanisms following <i>T. gondii</i> infection in host cells and the clinical diagnosis and treatment of pulmonary toxoplasmosis.</p><p><strong>Methods: </strong>Mouse alveolar macrophages served as blank controls, and mouse alveolar macrophages transfected with the empty lentiviral expression vector served as negative controls, and mouse alveolar macrophages transfected with lentiviral vectors overexpressing <i>T. gondii</i> type I and II ROP16 served as the type I and II ROP16 overexpression groups. Following puromycin selection, stably transfected cells that overexpressed type I and II ROP16 were generated, observed for green fluorescence expression under a fluorescence microscope and verified using PCR, Western blotting and real-time quantitative reverse transcription PCR (RT-qPCR) assays. The expression of ROP16, inducible nitric oxide synthase (iNOS), arginase (Arg)-1, mannose receptor (CD206), cluster of differentiation 86 (CD86), NOD-like receptor thermal protein domain associated protein 3 (NLRP3), caspase-1, apoptosis-associated speck-like protein containing a CARD (ASC), and interleukin (IL)-1β proteins was determined in mouse alveolar macrophages using Western blotting assay, and the mRNA levels of <i>ROP16</i>, <i>iNOS</i>, <i>IL-1β</i>, <i>IL-4</i>, <i>IL-12</i>, <i>IL-18</i>, <i>Arg-1</i>, <i>IL-10</i>, <i>IL-6</i>, tumor necrosis factor (<i>TNF</i>)-<i>α</i> and transforming growth factor (<i>TGF</i>)-<i>β</i> were detected in mouse alveolar macrophages using RT-qPCR assay.</p><p><strong>Results: </strong>Fluorescence microscopy showed 90% of mouse alveolar macrophages producing green fluorescent signals in the type Iand II ROP16 overexpression groups and the negative control group. The relative ROP16 protein expression was 1.000 ± 0.000, 1.003 ± 0.020, 1.349 ± 0.055, and 1.376 ± 0.080 in mouse alveolar macrophages in the blank control group, negative control group, and type Iand IIROP16 overexpression groups (<i>F</i> = 35.30, <i>P</i> < 0.01), and the relative <i>ROP16 mRNA</i> expression was 1.007 ± 0.172, 2.030 ± 0.356, 1 409.579 ± 75.960, and 1 413.581 ± 27.712 in the blank control group, negative control group, and type Iand II ROP16 overexpression groups (<i>F</i> = 811.00, <i>P</i> < 0.01). The ROP16 expression was significantly higher in the type Iand IIROP16 overexpression groups than in the blank control group at both protein and mRNA levels (all <i>P</i> value < 0.01). Western blotting assay detected significant differences among the four groups in terms of iNOS, Arg-1, CD86, CD206, NLRP3, caspase-1, ASC, and IL-1β protein expression (<i>F</i> = 124.70, 82.40, 79.82, 919.40, 84.74, 39.85, 2 354.00 and 65.96, all <i>P</i> values < 0.05), and th","PeriodicalId":38874,"journal":{"name":"中国血吸虫病防治杂志","volume":"37 2","pages":"127-135"},"PeriodicalIF":0.0,"publicationDate":"2025-03-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144162774","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-03-11DOI: 10.16250/j.32.1915.2024164
H Wu, J Wang, K Yang, X Wang, N Fang, L Duan, C Zhang, X Wang
Objective: To establish a method for determination of pyriclobenzuron (PBU) residues in rice and paddy environments, and to determine the residual amounts and observe the degradation dynamics of PBU.
Methods: In July 2022, the paddies of Zhejiang Academy of Agricultural Sciences were selected as experimental fields, and were divided into the blank control group (no pesticide application), the 1-fold-concentration pesticide group (1 kg/667 m2), and the 5-fold-concentration pesticide group (5 kg/667 m2), with a 100 m2 area in each group. At the early tillering stage of rice, 20% suspension of PBU sulfate was sprayed once in the 1-fold-concentration and 5-fold-concentration pesticide groups, and rice plants, paddy water and soil samples were collected 2 h, and 1, 2, 3, 5, 7, 11, 14, 21, 28, 35, 49 d and 63 d following spraying PBU, while rice straw, field soil, brown rice and rice husk samples were collected 98 d following spraying. PBU was extracted and purified in samples using a quick, easy, cheap, effective, rugged, and safe (QuEChERS) pretreatment technique, and the PBU contents were determined in samples using ultrahigh performance liquid chromatography tandem mass spectrometry (UPLC-MS/MS). The solvent standard working solution and matrix standard working solution were prepared. A linear regression equation was fitted between PBU concentration (x-axis) and peak area (y-axis), and the ratio of the slope (k) of the matrix standard curve to the slope (K) of the solvent standard curve was calculated to evaluate the matrix effect of PBU in samples. According to the Guidelines for Pesticide Residue Testing in Crops (NY/T 788-2018), the addition levels of PBU were set at 0.005, 0.050, 5.000, 1 000.000 mg/kg in rice plants, 0.005, 0.050, 2.000, 10.000 mg/kg in paddy water, 0.005, 0.050, 2.000 mg/kg in soil, and 0.005, 0.050, 5.000 mg/kg in brown rice and rice husks. The recovery and relative standard deviation (RSD) of PBU addition were calculated to evaluate the effectiveness of UPLC-MS/MS for determination of PBU contents. The first-order kinetic equation of PBU concentration was fitted in samples at different sampling time points to analyze the trends in PBU degradation in rice plants, paddy water, and soil, and the half-life of PBU was calculated in different samples.
Results: There was a good linear relationship between the mass concentration and peak area of PBU at concentrations of 0.000 1 to 0.020 0 mg/kg under solvent and matrix conditions (R2 = 0.985 8 to 0.999 7, t = -0.47 to 1.62, all P values < 0.01). The matrix effects of PBU were 70.26%, 65.42% and 65.12% in rice plants, brown rice and rice husks, indicating a matrix-inhibitory effect, and the matrix effect was 87.06% in soils, indicating a weak matrix effect. The recovery of PBU addition was 77.61% to 100.12% in different sample
{"title":"[Degradation dynamics and residue determination of pyriclobenzuron in rice and paddy environments].","authors":"H Wu, J Wang, K Yang, X Wang, N Fang, L Duan, C Zhang, X Wang","doi":"10.16250/j.32.1915.2024164","DOIUrl":"https://doi.org/10.16250/j.32.1915.2024164","url":null,"abstract":"<p><strong>Objective: </strong>To establish a method for determination of pyriclobenzuron (PBU) residues in rice and paddy environments, and to determine the residual amounts and observe the degradation dynamics of PBU.</p><p><strong>Methods: </strong>In July 2022, the paddies of Zhejiang Academy of Agricultural Sciences were selected as experimental fields, and were divided into the blank control group (no pesticide application), the 1-fold-concentration pesticide group (1 kg/667 m<sup>2</sup>), and the 5-fold-concentration pesticide group (5 kg/667 m<sup>2</sup>), with a 100 m<sup>2</sup> area in each group. At the early tillering stage of rice, 20% suspension of PBU sulfate was sprayed once in the 1-fold-concentration and 5-fold-concentration pesticide groups, and rice plants, paddy water and soil samples were collected 2 h, and 1, 2, 3, 5, 7, 11, 14, 21, 28, 35, 49 d and 63 d following spraying PBU, while rice straw, field soil, brown rice and rice husk samples were collected 98 d following spraying. PBU was extracted and purified in samples using a quick, easy, cheap, effective, rugged, and safe (QuEChERS) pretreatment technique, and the PBU contents were determined in samples using ultrahigh performance liquid chromatography tandem mass spectrometry (UPLC-MS/MS). The solvent standard working solution and matrix standard working solution were prepared. A linear regression equation was fitted between PBU concentration (x-axis) and peak area (y-axis), and the ratio of the slope (<i>k</i>) of the matrix standard curve to the slope (<i>K</i>) of the solvent standard curve was calculated to evaluate the matrix effect of PBU in samples. According to the <i>Guidelines for Pesticide Residue Testing in Crops (NY/T 788</i>-<i>2018)</i>, the addition levels of PBU were set at 0.005, 0.050, 5.000, 1 000.000 mg/kg in rice plants, 0.005, 0.050, 2.000, 10.000 mg/kg in paddy water, 0.005, 0.050, 2.000 mg/kg in soil, and 0.005, 0.050, 5.000 mg/kg in brown rice and rice husks. The recovery and relative standard deviation (RSD) of PBU addition were calculated to evaluate the effectiveness of UPLC-MS/MS for determination of PBU contents. The first-order kinetic equation of PBU concentration was fitted in samples at different sampling time points to analyze the trends in PBU degradation in rice plants, paddy water, and soil, and the half-life of PBU was calculated in different samples.</p><p><strong>Results: </strong>There was a good linear relationship between the mass concentration and peak area of PBU at concentrations of 0.000 1 to 0.020 0 mg/kg under solvent and matrix conditions (<i>R</i><sup>2</sup> = 0.985 8 to 0.999 7, <i>t</i> = -0.47 to 1.62, all <i>P</i> values < 0.01). The matrix effects of PBU were 70.26%, 65.42% and 65.12% in rice plants, brown rice and rice husks, indicating a matrix-inhibitory effect, and the matrix effect was 87.06% in soils, indicating a weak matrix effect. The recovery of PBU addition was 77.61% to 100.12% in different sample","PeriodicalId":38874,"journal":{"name":"中国血吸虫病防治杂志","volume":"37 2","pages":"201-208"},"PeriodicalIF":0.0,"publicationDate":"2025-03-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144162769","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-02-28DOI: 10.16250/j.32.1915.2024260
P Yang, F He, Q Yan, H Geng, T Gao, Q Gao, C Xiong, H Peng
Objective: To analyze the virus subtypes, molecular evolutional and molecular transmission network features of the first confirmed mpox case in Huai'an City, Jiangsu Province, so as to provide insights into understanding of the transmission and evolution dynamics of mpox virus and formulation of the mpox control strategy in the city.
Methods: Genomic DNA was extracted from swabs of the first confirmed mpox case's skin lesions in Huai'an City, and the amplicon sequencing library was constructed using the hypersensitive mpox virus whole-genome capture kit. High-throughput sequencing was performed using the GridION X5 nanopore sequencer on the Nanopore sequencing platform, and single nucleotide polymorphism (SNP) analysis of mpox virus genome sequences was performed following sequence assembly. In addition, phylogenetic analysis, genetic genealogy and molecular traceability analysis were performed.
Results: The virus whole genome sequence of the first confirmed mpox case was successfully obtained by high-throughput sequencing, with a full length of 197 182 bp, and was named hMpxV/China/JS-HA01/2023, which belonged to the clade IIb (West African clade) lineage B.1.3. Compared with the mpox virus reference sequence MPXV-M5312_HM12_Rivers-001 (GenBank accession number: NC_063383), the genome sequence of the Huai'an virus isolate carried 86 SNPs, including 40 SNPs in the coding region as non-synonymous mutations and 73 SNPs as nucleotide mutations caused by APOBEC3 (APOBEC3). Of the 97 mpox virus gene sequences, 79 sequences were included in the molecular network (81.44%), and the threshold of the genetic distance accessed to the network was 0.35/105. There were two large molecular transmission clusters and one scattered cluster in the molecular transmission network of the mpox virus, andthehMpxV/China/JS-HA01/2023 sequence was located in the large cluster. The 97 gene sequences formed 92 haplotypes, including three shared haplotypes Hap_4, Hap_6 and Hap_38, and an exclusive haplotype Hap_1 of hMpxV/China/JS-HA01/2023 generated from mutation of the exclusive haplotype Hap_43, while the exclusive haplotype Hap_43 was generated from mutation of the shared haplotype Hap_38.
Conclusions: The whole genome sequence of the mpox virus isolated from the first confirmed mpox case in Huai'an City has been successfully obtained, and the molecular evolutionary and molecular transmission network characteristics of the virus have been preliminarily understood.
{"title":"[Etiological characteristics and molecular evolution of the first mpox case in Huai'an City of Jiangsu Province].","authors":"P Yang, F He, Q Yan, H Geng, T Gao, Q Gao, C Xiong, H Peng","doi":"10.16250/j.32.1915.2024260","DOIUrl":"10.16250/j.32.1915.2024260","url":null,"abstract":"<p><strong>Objective: </strong>To analyze the virus subtypes, molecular evolutional and molecular transmission network features of the first confirmed mpox case in Huai'an City, Jiangsu Province, so as to provide insights into understanding of the transmission and evolution dynamics of mpox virus and formulation of the mpox control strategy in the city.</p><p><strong>Methods: </strong>Genomic DNA was extracted from swabs of the first confirmed mpox case's skin lesions in Huai'an City, and the amplicon sequencing library was constructed using the hypersensitive mpox virus whole-genome capture kit. High-throughput sequencing was performed using the GridION X5 nanopore sequencer on the Nanopore sequencing platform, and single nucleotide polymorphism (SNP) analysis of mpox virus genome sequences was performed following sequence assembly. In addition, phylogenetic analysis, genetic genealogy and molecular traceability analysis were performed.</p><p><strong>Results: </strong>The virus whole genome sequence of the first confirmed mpox case was successfully obtained by high-throughput sequencing, with a full length of 197 182 bp, and was named hMpxV/China/JS-HA01/2023, which belonged to the clade IIb (West African clade) lineage B.1.3. Compared with the mpox virus reference sequence MPXV-M5312_HM12_Rivers-001 (GenBank accession number: NC_063383), the genome sequence of the Huai'an virus isolate carried 86 SNPs, including 40 SNPs in the coding region as non-synonymous mutations and 73 SNPs as nucleotide mutations caused by APOBEC3 (APOBEC3). Of the 97 mpox virus gene sequences, 79 sequences were included in the molecular network (81.44%), and the threshold of the genetic distance accessed to the network was 0.35/10<sup>5</sup>. There were two large molecular transmission clusters and one scattered cluster in the molecular transmission network of the mpox virus, andthehMpxV/China/JS-HA01/2023 sequence was located in the large cluster. The 97 gene sequences formed 92 haplotypes, including three shared haplotypes Hap_4, Hap_6 and Hap_38, and an exclusive haplotype Hap_1 of hMpxV/China/JS-HA01/2023 generated from mutation of the exclusive haplotype Hap_43, while the exclusive haplotype Hap_43 was generated from mutation of the shared haplotype Hap_38.</p><p><strong>Conclusions: </strong>The whole genome sequence of the mpox virus isolated from the first confirmed mpox case in Huai'an City has been successfully obtained, and the molecular evolutionary and molecular transmission network characteristics of the virus have been preliminarily understood.</p>","PeriodicalId":38874,"journal":{"name":"中国血吸虫病防治杂志","volume":"37 1","pages":"85-92"},"PeriodicalIF":0.0,"publicationDate":"2025-02-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144031685","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-02-28DOI: 10.16250/j.32.1915.2024191
Z Liu, H Xie, X Sun, T Xia, J Guo
Tick-borne encephalitis is a central nervous system disease caused by infections with tick-borne pathogens, which is characterized by severe clinical symptoms, multiple sequelae, and a high fatality rate. Currently, there is no cure for tick-borne encephalitis. Tick-borne encephalitis virus (TBEV) is the most common pathogen of tick-borne encephalitis. Therefore, rapid and accurate detection of TBEV contributes to reducing the mortality of tick-borne encephalitis, improving patients' prognosis, and reducing the risk of TBEV transmission. The currently available serological tests for detection of TBEV infections mainly include neutralization test, enzyme-linked immunosorbent assay (ELISA), immunofluorescence assay, and nucleic acid tests mainly include polymerase chain reaction (PCR), loop-mediated isothermal amplification (LAMP), reverse transcription polymerase spiral reaction, clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated proteins (Cas)-based assays. This review summarizes the progress of researches on serological and nucleic acid tests for detection of TBEV infections, so as to provide insights into prevention and control of tick-borne encephalitis.
{"title":"[Research progress on techniques for detection of tick-borne encephalitis virus infections].","authors":"Z Liu, H Xie, X Sun, T Xia, J Guo","doi":"10.16250/j.32.1915.2024191","DOIUrl":"https://doi.org/10.16250/j.32.1915.2024191","url":null,"abstract":"<p><p>Tick-borne encephalitis is a central nervous system disease caused by infections with tick-borne pathogens, which is characterized by severe clinical symptoms, multiple sequelae, and a high fatality rate. Currently, there is no cure for tick-borne encephalitis. Tick-borne encephalitis virus (TBEV) is the most common pathogen of tick-borne encephalitis. Therefore, rapid and accurate detection of TBEV contributes to reducing the mortality of tick-borne encephalitis, improving patients' prognosis, and reducing the risk of TBEV transmission. The currently available serological tests for detection of TBEV infections mainly include neutralization test, enzyme-linked immunosorbent assay (ELISA), immunofluorescence assay, and nucleic acid tests mainly include polymerase chain reaction (PCR), loop-mediated isothermal amplification (LAMP), reverse transcription polymerase spiral reaction, clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated proteins (Cas)-based assays. This review summarizes the progress of researches on serological and nucleic acid tests for detection of TBEV infections, so as to provide insights into prevention and control of tick-borne encephalitis.</p>","PeriodicalId":38874,"journal":{"name":"中国血吸虫病防治杂志","volume":"37 2","pages":"209-216"},"PeriodicalIF":0.0,"publicationDate":"2025-02-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144162731","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}