1.DNA sequences of Paragonimus skrjabini populations from five provinces in China.
Ming-gang CHEN ; Zheng-shan CHANG ; Ai-li CUI ; David BLAIR ; Yong-nian ZHANG ; Shao-hong CHEN ; Zheng FENG
Chinese Medical Journal 2004;117(2):219-224
BACKGROUNDTo study differences among Paragonimus skrjabini (P. skrjabini) populations from five provinces in China (Guangdong, Fujian, Yunnan, Hubei, and Sichuan) and Paragonimus szechuanensis.
METHODSDNA sequences were obtained from the ITS2 and CO1 genes and phylogenetic trees were constructed from the results. Sequences were also obtained from several other species of Paragonimus for comparative purposes.
RESULTSAlthough differences existed in the DNA sequence among P. skrjabini populations from five provinces, the differences were very small. There was also some resemblance between P. miyazakii from Japan and Fujian strains of P. skrjabini.
CONCLUSIONAll studied populations can be regarded as different strains of P. skrjabini; P. szechuanensis is not a separate species but may be a geographical strain of P. skrjabini. We also found that P. miyazakii may be synonymous with P. skrjabini.
Animals ; Base Sequence ; genetics ; China ; Paragonimus ; genetics ; Philology
2.Sequence analysis of Paragonimus internal transcribed spacer 2 and cyclooxygenase 1 genes in freshwater crabs in Henan Province.
W CHEN ; T JIANG ; Y DENG ; Y ZHANG ; L AI ; P JI ; D WANG
Chinese Journal of Schistosomiasis Control 2023;35(5):501-507
OBJECTIVE:
To investigate the sequences of internal transcribed spacer 2 (ITS2) and cyclooxygenase 1 (COX1) genes of Paragonimus metacercariae in freshwater crabs in Henan Province, identify the species of Paragonimus and evaluate its genetic relationships with Paragonimus isolates from other provinces in China.
METHODS:
Freshwater crabs were collected from 8 survey sites in Zhengzhou, Luoyang, Pingdingshan, Nanyang and Jiyuan cities of Henan Province from 2016 to 2021, and Paragonimus metacercariae were detected in freshwater crabs. Genomic DNA was extracted from Paragonimus metacercariae, and the ITS2 and COX1 genes were amplified using PCR assay, followed by sequencing of PCR amplification products. The gene sequences were spliced and aligned using the software DNASTAR, and aligned with the sequences of Paragonimus genes in the GenBank. Phylogenetic trees were created using the MEGA6 software with the Neighbor-Joining method based on ITS2 and COX1 gene sequences, with Fasciola hepatica as the outgroup.
RESULTS:
The detection rates of Paragonimus metacercariae were 6.83% (11/161), 50.82% (31/61), 18.52% (5/26), 8.76% (12/137), 14.29% (9/63), 17.76% (19/105), 18.50% (32/173) and 42.71% (41/96) in freshwater crabs from 8 survey sites in Zhengzhou, Luoyang, Pingdingshan, Nanyang and Jiyuan cities of Henan Province, with a mean detection rate of 19.46% (160/822), and a mean infection intensity of 0.57 metacercariae/g. The amplified ITS2 and COX1 gene fragments of Paragonimus were approximately 500 bp and 450 bp in lengths, respectively. The ITS2 gene sequences of Paragonimus metacercariae from 8 survey sites of Henan Province showed the highest homology (99.8% to 100.0%) with the gene sequence of P. skrjabini (GenBank accession number: MW960209.1), and phylogenetic analysis showed that the Paragonimus in this study was clustered into the same clade with P. skrjabini from Sichuan Province (GenBank accession number: AY618747.1), Guangxi Zhuang Autonomous Region (GenBank accession number: AY618729.1) and Hubei Province (GenBank accession number: AY618751.1), and P. miyazaki from Fujian Province (GenBank accession number: AY618741.1) and Japan (GenBank accession number: AB713405.1). The COX1 gene sequences of Paragonimus metacercariae from 8 survey sites of Henan Province showed the highest homology (90.0% to 100.0%) with the gene sequence of P. skrjabini (GenBank accession number: AY618798.1), and phylogenetic analysis showed that the Paragonimus in this study was clustered into the same clade with all P. skrjabini and clustered into the same sub-clade with P. skrjabini from Hubei Province (GenBank accession numbers: AY618782.1 and AY618764.1).
CONCLUSIONS
Paragonimus species from freshwater crabs in Henan Province were all characterized as P. skrjabini, and the ITS2 and COX1 gene sequences had the highest homology to those of P. skrjabini from Hubei Province. The results provide insights into study of Paragonimus in Henan Province and China.
Animals
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Paragonimus/genetics*
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Brachyura/genetics*
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Cyclooxygenase 1/genetics*
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Phylogeny
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China/epidemiology*
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Sequence Analysis, DNA
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Paragonimiasis
3.Phylogenetic relationship of ribosomal ITS2 and mitochondrial COI among diploid and triploid Paragonimus westermani isolates.
Gab Man PARK ; Kyung Il IM ; Tai Soon YONG
The Korean Journal of Parasitology 2003;41(1):47-55
We compared patterns of intraspecific polymorphism of two markers with contrasting modes of evolution, nuclear ribosomal DNA (rDNA) and mitochondrial DNA (mtDNA), in the lung fluke, diploid and triploid Paragonimus westermani from three geographical regions of Korea. The genetic distances between three populations of Korean diploid and triploid P. westermani showed no significant difference in the nucleotide sequences of the mitochondrial cytochrome c oxidase subunit I (mtCOI) and ribosomaal second internal transcribed spacer (ITS2) genes. A highly resolved strict-consensus tree was obtained that illustrated phylogenetically useful information of the ITS2 and mtCOI sequences from diploid and triploid P. westermani.
Animals
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DNA, Mitochondrial/*genetics
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DNA, Ribosomal Spacer/*genetics
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*Diploidy
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Electron Transport Complex IV/*genetics
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Evolution, Molecular
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Genes, Helminth/genetics
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Korea
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Paragonimus/*genetics
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*Phylogeny
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*Polyploidy
4.Paragonimus and Paragonimiasis in Vietnam: an Update.
Pham Ngoc DOANH ; Yoichiro HORII ; Yukifumi NAWA
The Korean Journal of Parasitology 2013;51(6):621-627
Paragonimiasis is a food-borne parasitic zoonosis caused by infection with lung flukes of the genus Paragonimus. In Vietnam, research on Paragonimus and paragonimiasis has been conducted in northern and central regions of the country. Using a combination of morphological and molecular methods, 7 Paragonimus species, namely P. heterotremus, P. westermani, P. skrjabini, P. vietnamensis, P. proliferus, P. bangkokenis and P. harinasutai, have been identified in Vietnam. Of these, the first 3, P. heterotremus, P. westermani and P. skrjabini, are known to infect humans in other countries. However, in Vietnam, only P. heterotremus, found in some northern provinces, has been shown to infect humans. Even nowadays, local people in some northern provinces, such as Lai Chau and Yen Bai, are still suffering from P. heterotremus infection. In some provinces of central Vietnam, the prevalence and infection intensity of P. westermani metacercariae in freshwater crabs (the second intermediate hosts) are extremely high, but human cases have not been reported. Likewise, although P. skrjabini was found in Thanh Hoa Province, its pathogenicity to humans in Vietnam still remains uncertain. The results of molecular phylogenetic analyses of Vietnamese Paragonimus species provides new insights on the phylogeny and taxonomy of the genus Paragonimus. Comprehensive molecular epidemiological and geobiological studies on the genus in Vietnam and adjacent countries are needed to clarify the biodiversity and public health significance of the lung flukes.
Animals
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Humans
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Paragonimiasis/*epidemiology
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Paragonimus/classification/genetics/*isolation & purification
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Phylogeny
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Prevalence
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Sequence Analysis, DNA
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Shellfish/parasitology
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Vietnam/epidemiology
5.Molecular and biochemical characterization of hemoglobinase, a cysteine proteinase, in Paragonimus westermani.
Joon Hyuck CHOI ; Jae Hyuk LEE ; Hak Sun YU ; Hae Jin JEONG ; Jin KIM ; Yeon Chul HONG ; Hyun Hee KONG ; Dong Il CHUNG
The Korean Journal of Parasitology 2006;44(3):187-196
The mammalian trematode Paragonimus westermani is a typical digenetic parasite, which can cause paragonimiasis in humans. Host tissues and blood cells are important sources of nutrients for development, growth and reproduction of P. westermani. In this study, a cDNA clone encoding a 47 kDa hemoglobinase of P. westermani was characterized by sequencing analysis, and its localization was investigated immunohistochemically. The phylogenetic tree prepared based on the hemoglobinase gene showed high homology with hemoglobinases of Fasciola hepatica and Schistosoma spp. Moreover, recombinant P. westermani hemoglobinase degradaded human hemoglobin at acidic pH (from 3.0 to 5.5) and its activity was almost completely inhibited by E-64, a cysteine proteinase inhibitor. Immunohistochemical studies showed that P. westermani hemoglobinase was localized in the epithelium of the adult worm intestine implying that the protein has a specific function. These observations suggest that hemoglobinase may act as a digestive enzyme for acquisition of nutrients from host hemoglobin. Further investigations may provide insights into hemoglobin catabolism in P. westermani.
Sequence Alignment
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Recombinant Proteins/biosynthesis/genetics
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Phylogeny
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Paragonimus westermani/*enzymology/genetics
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Molecular Sequence Data
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Hemoglobins/metabolism
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Escherichia coli/enzymology/genetics
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DNA, Complementary/genetics
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Cysteine Endopeptidases/*genetics/immunology/*metabolism
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Astacoidea/parasitology
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Antigens, Helminth/genetics/immunology/metabolism
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Animals
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Amino Acid Sequence
6.Molecular Variation in the Paragonimus heterotremus Complex in Thailand and Myanmar.
Oranuch SANPOOL ; Pewpan M INTAPAN ; Tongjit THANCHOMNANG ; Penchom JANWAN ; Yukifumi NAWA ; David BLAIR ; Wanchai MALEEWONG
The Korean Journal of Parasitology 2013;51(6):677-681
Paragonimiasis is an important food-borne parasitic zoonosis caused by infection with lung flukes of the genus Paragonimus. Of the 7 members of the genus known in Thailand until recently, only P. heterotremus has been confirmed as causing human disease. An 8th species, P. pseudoheterotremus, has recently been proposed from Thailand, and has been found in humans. Molecular data place this species as a sister species to P. heterotremus, and it is likely that P. pseudoheterotremus is not specifically distinct from P. heterotremus. In this study, we collected metacercariae of both nominal species (identification based on metacercarial morphology) from freshwater crabs from Phetchabun Province in northern Thailand, Saraburi Province in central Thailand, and Surat Thani Province in southern Thailand. In addition, we purchased freshwater crabs imported from Myanmar at Myawaddy Province, western Thailand, close to the Myanmar-Thailand border. The DNAs extracted from excysted metacercariae were PCR-amplified and sequenced for ITS2 and cox1 genes. The ITS2 sequences were nearly identical among all samples (99-100%). Phylogenies inferred from all available partial cox1 sequences contained several clusters. Sequences from Indian P. heterotremus formed a sister group to sequences from P. pseudoheterotremus-type metacercariae. Sequences of P. heterotremus from Thailand, Vietnam, and China formed a separate distinct clade. One metacercaria from Phitsanulok Province was distinct from all others. There is clearly considerable genetic variation in the P. heterotremus complex in Thailand and the form referred to as P. pseudoheterotremus is widely distributed in Thailand and the Thai-Myanmar border region.
Animals
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Cluster Analysis
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DNA, Ribosomal Spacer/chemistry/genetics
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Electron Transport Complex IV/genetics
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*Genetic Variation
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Metacercariae/genetics/isolation & purification
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Molecular Sequence Data
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Myanmar
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Paragonimus/*classification/*genetics/isolation & purification
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Phylogeny
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Polymerase Chain Reaction
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Sequence Analysis, DNA
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Sequence Homology
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Shellfish/parasitology
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Thailand
7.Divergent long-terminal-repeat retrotransposon families in the genome of Paragonimus westermani.
The Korean Journal of Parasitology 2003;41(4):221-231
To gain information on retrotransposons in the genome of Paragonimus westermani, PCR was carried out with degenerate primers, specific to protease and reverse transcriptase (rt) genes of long-terminal-repeat (LTR) retrotransposons. The PCR products were cloned and sequenced, after which 12 different retrotransposon-related sequences were isolated from the trematode genome. These showed various degrees of identity to the polyprotein of divergent retrotransposon families. A phylogenetic analysis demonstrated that these sequences could be classified into three different families of LTR retrotransposons, namely, Xena, Bel, and Gypsy families. Of these, two mRNA transcripts were detected by reverse transcriptase-PCR, showing that these two elements preserved their mobile activities. The genomic distributions of these two sequences were found to be highly repetitive. These results suggest that there are diverse retrotransposons including the ancient Xena family in the genome of P. westermani, which may have been involved in the evolution of the host genome.
Amino Acid Sequence
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Animals
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Cloning, Molecular
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DNA, Helminth/analysis
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*Evolution, Molecular
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*Genome
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Molecular Sequence Data
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Paragonimus/*genetics
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Phylogeny
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RNA-Directed DNA Polymerase/chemistry/genetics
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Retroelements/*genetics
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Sequence Alignment
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Sequence Analysis, DNA
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Terminal Repeat Sequences/*genetics
8.Paragonimus paishuihoensis Metacercariae in Freshwater Crabs, Potamon lipkei, in Vientiane Province, Lao PDR.
Shigehisa HABE ; Pham Ngoc DOANH ; Shinichiro YAHIRO ; Nanthasane VANNAVONG ; Hubert BARENNES ; Peter ODERMATT ; Gilles DREYFUSS ; Yoichiro HORII ; Yukifumi NAWA
The Korean Journal of Parasitology 2013;51(6):683-687
Among Paragonimus species, P. paishuihoensis is one of the most mysterious and poorly understood species. Metacercariae are characterized by having a unique dendritically branched excretory bladder. However, the morphology of the adult worm remains unknown. To date, metacercariae of this species have been reported only in China and Thailand. In this study, we first found P. paishuihoensis metacercariae in freshwater crabs, Potamon lipkei, in Hinheub District, Vientiane, Lao PDR, with a prevalence of 77.7% and the average intensity of 10.3 (range 1-28) metacercariae per crab. The molecular data based on ITS2 and CO1 markers indicated that P. paishuihoensis from Laos and Thailand were almost completely identical and were close to members of the Paragonimus bangkokensis/Paragonimus harinasutai complex. Attempts to infect experimental animals (cats, dogs, and rats) with P. paishuihoensis were unsuccessful, suggesting that these animals might be unsuitable definitive hosts for the species. Further studies are necessary to elucidate the taxonomic status and life cycle of P. paishuihoensis.
Animals
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Brachyura/*parasitology
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Cluster Analysis
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DNA, Ribosomal Spacer/chemistry/genetics
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Electron Transport Complex IV/genetics
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Fresh Water
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Laos
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Metacercariae/*isolation & purification
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Molecular Sequence Data
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Paragonimus/*isolation & purification
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Phylogeny
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Polymerase Chain Reaction
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Prevalence
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Sequence Analysis, DNA
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Sequence Homology