“夜逸蚴”日本血吸虫线粒体基因组特征与系统进化的关系

doi:10.12140/j.issn.1000-7423.2023.06.006

中国寄生虫学与寄生虫病杂志 ›› 2023, Vol. 41 ›› Issue (6): 699-707.doi: 10.12140/j.issn.1000-7423.2023.06.006

“夜逸蚴”日本血吸虫线粒体基因组特征与系统进化的关系

王宁(), 彭晗琪, 高常哲, 程羽珩, 吕大兵^*()

苏州大学公共卫生学院流行病与卫生统计学系，江苏苏州 215127

收稿日期:2023-07-14 修回日期:2023-09-12 出版日期:2023-12-30 发布日期:2023-12-22
通讯作者: * 吕大兵（1967-），男，博士，教授，从事血吸虫群体遗传学与流行病学、血吸虫病传播动力学建模分析研究。E-mail: ludabing@suda.edu.cn
作者简介:王宁（1996-），女，硕士研究生，从事血吸虫群体遗传学与流行病学研究。E-mail: nnff202018@163.com
基金资助:
国家自然科学基金(81971957)

Characterization of the mitochondrial genome and phylogenetic implication of Schistosoma japonicum featured with “nocturnal cercarial emergence”

WANG Ning(), PENG Hanqi, GAO Changzhe, CHENG Yuheng, LYU Dabing^*()

Department of Epidemiology and Health Statistics, School of Public Health, Soochow University，Suzhou 215127, Jiangsu, China

Received:2023-07-14 Revised:2023-09-12 Online:2023-12-30 Published:2023-12-22
Contact: * E-mail: ludabing@suda.edu.cn
Supported by:
National Natural Science Foundation of China(81971957)

摘要/Abstract

摘要：

目的测定具有“夜逸蚴”特征的日本血吸虫线粒体全基因组序列，并探讨其与大陆其他日本血吸虫地域株的系统进化关系，为后续进行种群遗传结构与遗传多样性研究提供新的数据。方法 2020年于安徽省石台县现场采集钉螺，实验室内分离感染性钉螺，逸出的尾蚴以腹部贴片法感染ICR小鼠，灌注法获取肝门静脉和肠系膜静脉处虫体，随机抽样进行测序。使用血液/组织基因组DNA提取试剂盒提取血吸虫DNA，采用Illumina NovaSeq 6000测序平台进行双末端测序，采用GetOrganelle软件组装线粒体基因组，使用MEGA 11软件分析线粒体基因组结构特征与碱基组成。选择已发表的中国地区17个日本血吸虫线粒体基因组序列，采用最大似然法（ML）和邻接法（NJ）构建系统进化树。结果安徽省石台县分离的“夜逸蚴”日本血吸虫线粒体基因组全长14 085 bp（GenBank登录号：ON637109），编码36个基因，由12个蛋白编码基因（PCG），22个tRNA基因和2个rRNA基因组成。线粒体基因组A + T含量为71.35%，存在基因重叠区2处、基因间隔区29处；在22个tRNA基因中，除trnaC和trnaS1基因缺失二氢尿嘧啶（DHU）臂外，其余均能形成典型三叶草二级结构。蛋白编码基因中，cytb、nad4、nad2和nad6基因的终止密码子为TAA，不同于以TAG为终止密码子的中国其他地域株。基于NJ法和ML法构建的系统进化树具有相似的拓扑结构，石台县“夜逸蚴”日本血吸虫分离株单独成一支；中国台湾血吸虫株与中国大陆其他地域株分离，形成一支。结论安徽省石台地区的日本血吸虫分离株其终止密码子与中国其他地域株存在差异，线粒体基因组的系统进化地位分析，与其他地域株亲缘关系较远，遗传差异较大。

关键词: 线粒体基因组, 序列分析, 系统进化关系, 日本血吸虫, 夜逸蚴特征

Abstract:

Objective This study aimed to determine the complete mitochondrial genome sequence of Schistosoma japonicum featured with nocturnal cercarial emergence pattern and to explore its phylogenetic relationship with other S. japonicum geographical isolates from mainland China, providing new reference data for further study on population genetic structure and genetic diversity. Methods Field Oncomelania hupensis snails were collected from Shitai County of Anhui in 2020, and the infected snails were separated in the laboratory. ICR mice were infected with cercariae shed from the infected snails using abdominal patch method. The worms were obtained by perfusion from hepatic portal and mesenteric vein and randomly sampled for sequencing. The worm genomic DNA was extracted with blood/tissue DNA extraction Kit, and sequenced at paied-end using Illumina NovaSeq 6000 sequencing platform. The mitochondrial genome was assembled using GetOrganelle tool, and its structural features and base composition were analyzed using MEGA 11 software. The phylogenetic tree was constructed using the neighbour-joining (NJ) and maximum likelihood (ML) method based on 17 published mitochondrial genome sequences of S. japonicum from other parts of China. Results The complete circular mitochondrial genome of S. japonicum with nocturnal cercarial emergence pattern isolated from Shitai County of Anhui was 14 085 bp in length(Genbank accession no. ON637109), encoding 36 genes, consisting of 12 protein-coding genes (PCGs), two ribosomal RNA (rRNA) genes, 22 transfer RNA (tRNA) genes, with the AT content of 71.35%. There were two gene-overlapping regions and 29 intergenic regions in the mitochondrial genome. Among the 22 tRNA genes, except for trnaC and trnaS1 genes, which missed the dihydrouridine (DHU) arm, the rest were able to form a typical cloverleaf secondary structure. Among the PCGs, the stop codon of cytb, nad4, nad2 and nad6 was TAA, which differed from other geographical strains in China with TAG as the stop codon. Phylogenetic trees constructed based on NJ and ML had similar topologies. The isolated strain of S. japonicum featured with “nocturnal cercarial emergence” in Shitai County, forms a single strain. S. japonicum strains from Taiwan, China and other regions of Chinese Mainland are separated to form one branch. Conclusion The stop codons of S. japonicum isolate from Shitai area of Anhui Province differed from those of other geographical isolates in China. Additionally, based on the phylogenetic analysis, the isolate featured with nocturnal cercarial emergence exhibited a more distant relationship with other regional isolates, showing greater

Key words: Mitochondrial genome, Sequence analysis, Phylogenetic relationship, Schistosoma japonicum, Nocturnal cercarial emergence

中图分类号:

R383.24

王宁, 彭晗琪, 高常哲, 程羽珩, 吕大兵. “夜逸蚴”日本血吸虫线粒体基因组特征与系统进化的关系[J]. 中国寄生虫学与寄生虫病杂志, 2023, 41(6): 699-707.

WANG Ning, PENG Hanqi, GAO Changzhe, CHENG Yuheng, LYU Dabing. Characterization of the mitochondrial genome and phylogenetic implication of Schistosoma japonicum featured with “nocturnal cercarial emergence”[J]. Chinese Journal of Parasitology and Parasitic Diseases, 2023, 41(6): 699-707.

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样品来源（缩写） Population location（Abbreviation）	经度 Longitude	纬度 Latitude	流行区类型 Types of ecological settings	GenBank登录号 GenBank accession no.
安徽石台 Shitai, Anhui（AHST）	117.49	30.21	山丘型 Hilly-type	ON637109（研究样品 Research sample）
安徽贵池 Guichi, Anhui（AHGC）	117.57	30.69	湖沼型 Lake-type	KU196299
安徽铜陵 Tongling, Anhui（AHTL）	117.80	30.95	湖沼型 Lake-type	KU196309
安徽枞阳 Zongyang, Anhui（AHZY）	117.25	30.71	湖沼型 Lake-type	KF279406
安徽无为 Wuwei, Anhui（AHWW）	117.90	31.31	湖沼型 Lake-type	KF279404
江苏无锡 Wuxi, Jiangsu（JSWX）	120.28	31.53	湖沼型 Lake-type	HM120843
浙江嘉善 Jiashan, Zhejiang（ZJJS）	120.93	30.84	湖沼型 Lake-type	HM120841
江西南昌 Nanchang, Jiangxi（JXNC）	115.95	28.55	湖沼型 Lake-type	KU196369
江西永修 Yongxiu, Jiangxi（JXYX）	115.83	29.02	湖沼型 Lake-type	HM120844
江西都昌 Duchang, Jiangxi（JXDC）	116.21	29.28	湖沼型 Lake-type	KU196360
湖南岳阳 Yueyang, Hunan（HNYY）	113.14	29.36	湖沼型 Lake-type	KU196338
湖南常德 Changde, Hunan（HNCD）	111.71	29.04	湖沼型 Lake-type	KU196328
湖北武汉 Wuhan, Hubei（HBWH）	114.31	30.60	湖沼型 Lake-type	HM120842
湖北沙市 Shashi, Hubei（HBSS）	112.25	30.31	湖沼型 Lake-type	KU196237
四川西昌 Xichang, Sichuan（SCXC）	102.20	27.50	山丘型 Hilly-type	KU196389
四川天全 Tianquan, Sichuan（SCTQ）	102.78	30.06	山丘型 Hilly-type	HM120846
云南洱源 Eryuan, Yunnan（YNEY）	99.95	26.12	山丘型 Hilly-type	KU196408
中国台湾 Taiwan, China（TW）	120.92	23.85	湖沼型 Lake-type	KU196407

基因 Gene	位置/nt Position/nt	长度/bp Length/bp	基因间隔/bp Intergenic sequences/bp	起始/终止密码子 Start and stop codons	反密码子 Anticodons	氨基酸数目 No. amino acid	(A + T)/%
trnR	1~65	65	11		TCG		66.15
nad5	77~1 663	1 587	42	ATG/TAG		528	73.03
trnG	1 706~1 775	70	7		TCC		70.00
cox3	1 783~2 433	651	14	ATG/TAA		216	72.35
trnE	2 448~2 516	69	9		TTC		62.32
trnH	2 526~2 590	65	5		GCG		75.38
cob	2 596~3 711	1 116	34	ATG/TAA		371	71.06
nad4L	3 746~4 009	264	-37	ATG/TAA		87	73.48
nad4	3 973~5 247	1 275	31	ATG/TAA		424	70.67
trnQ	5 279~5 345	67	62		TTG		58.21
trnF	5 408~5 468	61	0		GAA		65.57
trnM	5 469~5 535	67	0		CAT		73.13
atp6	5 536~6 054	519	15	ATG/TAA		172	72.45
nad2	6 070~6 924	855	3	ATG/TAA		284	72.87
trnA	6 928~6 995	68	18		TGC		73.53
trnD	7 014~7 078	65	1		GTC		63.08
nad1	7 080~7 982	891	-1	ATG/TAG		296	70.93
trnN	7 982~8 046	65	22		GTT		67.69
trnP	8 069~8 134	66	37		GAA		77.27
trnI	8 172~8 237	66	12		GAT		57.58
trnK	8 250~8 320	71	3		CTT		76.06
nad3	8 324~8 683	360	9	ATG/TAG		119	76.94
trnW	8 693~8 763	71	19		TCA		63.38
trnV	8 783~8 848	66	8		TAC		69.7
trnS1	8 857~8 919	63	6		GCT		69.84
cox1	8 926~10 569	1 644	60	GTG/TAG		547	68.49
trnT	10 630~10 698	69	0		TGT		73.91
rrnL	10 699~11 714	1 016	0				68.9
trnC	11 715~11 776	62	1		GCA		72.58
rrnS	11 778~12 518	741	4				66.67
cox2	12 523~13 131	609	10	ATG/TAA		202	69.13
nad6	13 142~13 600	459	68	ATG/TAA		152	76.03
trnY	13 669~13 735	67	14		GTA		71.64
trnL1	13 750~13 819	70	0		TAG		67.14
trnS2	13 820~13 887	68	129		TAA		75
trnL2	14 017~14 084	68	1		CAA		61.76

基因序列 Nucleotide sequence	A/%	T (U)/%	G/%	C/%	(A + T)/%	(G + C)/%	AT-skew	GC-skew
全基因组 Overall	25.14	46.21	20.37	8.28	71.35	28.65	-0.296	0.422
蛋白编码基因 Protein-coding gene	23.31	48.26	20.60	7.83	71.57	28.43	-0.349	0.451
密码子第一位点 Codon 1	26.63	41.11	24.08	8.18	67.74	32.26	-0.214	0.493
密码子第二位点 Codon 2	19.01	48.65	19.94	12.40	67.65	32.35	-0.438	0.233
密码子第三位点 Codon 3	24.31	55.01	17.77	2.91	79.33	20.67	-0.387	0.720
tRNA基因 tRNA genes	29.20	39.48	20.97	10.35	68.69	31.31	-0.150	0.339
rRNA基因 rRNA genes	29.76	38.19	20.72	11.33	67.96	32.04	-0.124	0.293

基因 Gene	A/%	T/%	G/%	C/%	(G + C)/%	AT-skew	GC-skew
nad5	21.30	51.73	20.54	6.43	26.97	-0.417	0.523
cox3	23.35	49.00	19.35	8.30	27.65	-0.355	0.400
cob	23.48	47.58	20.34	8.60	28.94	-0.339	0.406
nad4L	25.38	48.10	19.70	6.82	26.52	-0.309	0.486
nad4	23.92	46.74	21.18	8.16	29.33	-0.323	0.444
atp6	23.32	49.13	18.88	8.67	27.55	-0.356	0.371
nad2	21.05	51.81	20.24	6.90	27.13	-0.422	0.491
nad1	25.03	45.90	22.00	7.07	29.07	-0.294	0.514
nad3	23.89	53.06	18.05	5.00	23.06	-0.379	0.566
cox1	22.57	45.92	21.96	9.55	31.51	-0.341	0.394
cox2	27.75	41.38	21.35	9.52	30.87	-0.197	0.383
nad6	24.18	51.86	18.08	5.88	23.97	-0.364	0.509

“夜逸蚴”日本血吸虫线粒体基因组特征与系统进化的关系

Characterization of the mitochondrial genome and phylogenetic implication of Schistosoma japonicum featured with “nocturnal cercarial emergence”

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