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Volume 37(4); December 1999

Mini Reviews

Phylogeny, host-parasite relationship and zoogeography
Hideo Hasegawa
Korean J Parasitol 1999;37(4):197-213.
Published online December 31, 1999
DOI: https://doi.org/10.3347/kjp.1999.37.4.197

Phylogeny is the evolutionary history of a group or the lineage of organisms and is reconstructed based on morphological, molecular and other characteristics. The genealogical relationship of a group of taxa is often expressed as a phylogenetic tree. The difficulty in categorizing the phylogeny is mainly due to the existence of frequent homoplasies that deceive observers. At the present time, cladistic analysis is believed to be one of the most effective methods of reconstructing a phylogenetic tree. Excellent computer program software for phylogenetic analysis is available. As an example, cladistic analysis was applied for nematode genera of the family Acuariidae, and the phylogenetic tree formed was compared with the system used currently. Nematodes in the genera Nippostrongylus and Heligmonoides were also analyzed, and the validity of the reconstructed phylogenetic trees was observed from a zoogeographical point of view. Some of the theories of parasite evolution were briefly reviewed as well. Coevolution of parasites and humans was discussed with special reference to the evolutionary relationship between Enterobius and primates.

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To choose one or more appropriate molecular markers or gene regions for resolving a particular systematic question among the organisms at a certain categorical level is still a very difficult process. The primary goal of this review, therefore, is to provide a theoretical information in choosing one or more molecular markers or gene regions by illustrating general properties and phylogenetic utilities of nuclear ribosomal DNA (rDNA) and mitochondrial DNA (mtDNA) that have been most commonly used for phylogenetic researches. The highly conserved molecular markers and/or gene regions are useful for investigating phylogenetic relationships at higher categorical levels (deep branches of evolutionary history). On the other hand, the hypervariable molecular markers and/or gene regions are useful for elucidating phylogenetic relationships at lower categorical levels (recently diverged branches). In summary, different selective forces have led to the evolution of various molecular markers or gene regions with varying degrees of sequence conservation. Thus, appropriate molecular markers or gene regions should be chosen with even greater caution to deduce true phylogenetic relationships over a broad taxonomic spectrum.

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Original Articles

Isoenzyme patterns and phylogenetic relationships in Acanthamoeba spp. isolated from contact lens containers in Korea
Ho-Joon Shin, Myung-Soo Cho, Han-Jip Kim, Kyung-Il Im
Korean J Parasitol 1999;37(4):229-236.
Published online December 31, 1999
DOI: https://doi.org/10.3347/kjp.1999.37.4.229

In order to refer to the basic information regarding the identification of isolates obtained from a contact lens container in Korea, the isoelectric focusing gel electrophoresis was employed to compare the isoenzyme band patterns among Acanthamoeba spp. including eight isolates and the simple pairwise dissimilarity analysis was carried out. For an alkaline phosphate development, isolate 7 and Acanthamoeba polyphaga showed homologous band patterns, and isolates 1, 2, and 3 showed the same patterns. For lactate dehydrogenase, similar patterns were observed in isolates 2 and 3. Isolates 3 and 5 showed homologous band patterns for malate dehydrogenase and glucose phosphate isomerase. For hexokinase, isolates 4, 7, and A. hatchetti showed the same band patterns. In others, a considerable number of interstrain polymorphisms was observed in nine isoenzyme band patterns. In Acanthamoeba group II, genetic distances among isolates 1, 2, 3, 4, and 5 ranged from 0.104 to 0.200. In comparison to A. castellanii, A. hatchetti, and A. polyphaga, genetic distances of isolates 7 and 8 were 0.254 and 0.219, respectively. In Acanthamoeba group III, including A. culbertsoni, A. healyi, and A. royreba, isolate 6 had genetic distances which ranged from 0.314 to 0.336. Finally, when comparing to the six reference Acanthamoeba, it was possible to classify isolates 1, 2, 3, 4, and 5, as genetically close-related species and as independent species group. Furthermore, isolates 6, 7 and 8 were identified as independent species as well.

Citations

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  • Diagnosis of Acanthamoeba keratitis
    N. R. Marchenko, Evg. A. Kasparova
    Vestnik oftal'mologii.2016; 132(5): 103.     CrossRef
  • Natural occurrence of Mycobacterium as an endosymbiont of Acanthamoeba isolated from a contact lens storage case
    Hak Sun Yu, Hae Jin Jeong, Yeon-Chul Hong, Seong-Yong Seol, Dong-Il Chung, Hyun-Hee Kong
    The Korean Journal of Parasitology.2007; 45(1): 11.     CrossRef
  • Pathogenic free-living amoebae in Korea
    Ho-Joon Shin, Kyung-il Im
    The Korean Journal of Parasitology.2004; 42(3): 93.     CrossRef
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A cytogenetic study on human intestinal trematodes of the genus Metagonimus (Digenea: Heterophyidae) in Korea
Soo-Ung Lee, Sun Huh, Gab-Man Park, Jong-Yil Chai
Korean J Parasitol 1999;37(4):237-241.
Published online December 31, 1999
DOI: https://doi.org/10.3347/kjp.1999.37.4.237

In order to analyze chromosome numbers and karyotypes of intestinal trematodes belonging to the genus, Metagonimus, the gonad tissues of M. takahashii, M. miyatai, and M. yokogawai were prepared and examined. The number of bivalents in the first meiotic division of M. takahashii was nine (n=9). The diploid number of M. miyatai was observed to be eighteen (2n=18) and their chromosomes consisted of one pair of metacentric, 7 pairs of submetacentric, and one pair of telocentric chromosomes. The diploid number of M. yokogawai was thirty-two (2n=32) and the chromosome complements were composed of two pairs of metacentric, 11 pairs of submetacentric, and three pairs of subtelocentric chromosomes. These results could be a supporting evidence for the validity of the new species, M. miyatai, distinct from M. yokogawai

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    Sang-Mee Guk, Jin-Young Park, Min Seo, Eun-Taek Han, Jae-Lip Kim, Jong-Yil Chai
    Journal of Parasitology.2005; 91(1): 12.     CrossRef
  • Sequence comparisons of 28S ribosomal DNA and mitochondrial cytochrome c oxidase subunit I of Metagonimus yokogawai, M. takahashii and M. miyatai
    Soo-Ung Lee, Sun Huh, Woon-Mok Sohn, Jong-Yil Chai
    The Korean Journal of Parasitology.2004; 42(3): 129.     CrossRef
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    Jong-Yil Chai, Soon-Hyung Lee
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Usefulness of IgG4 subclass antibodies for diagnosis of human clonorchiasis
Sung-Tae Hong, Mejeong Lee, Nak-Jin Sung, Sang Rock Cho, Jong-Yil Chai, Soon-Hyung Lee
Korean J Parasitol 1999;37(4):243-248.
Published online December 31, 1999
DOI: https://doi.org/10.3347/kjp.1999.37.4.243

The present study analyzed serum IgG subclass antibody reaction to major antigenic bands of Clonorchis sinensis to investigate improvement of its serodiagnosis. Of the four subclass antibodies, IgG1 and IgG2 antibodies were produced but not specific, IgG3 antibody was least produced, and IgG4 antibody was prominent and specific. The serum IgG antibody reaction to any of 43-50, 34-37, 26-28, and 8 kDa bands was found in 65.5% of 168 egg positive cases while IgG4 antibody reaction was found in 22.0% of them. The positive rates of IgG and IgG4 antibodies were directly correlated with the intensity of infection. All of the sera from heavily infected cases over EPG 5,000 showed positive reaction for specific IgG and IgG4 antibodies. The specific serum IgG4 antibody disappeared within 6 months after treatment. The bands of 35 kDa and 67 kDa cross-reacted with IgG antibodies but not with IgG4 antibodies in sera of other trematode infections. The present findings suggest that serum IgG4 antibody reaction to 8 kDa band is specific but not sensitive. Any method to increase its sensitivity is required for improved serodiagnosis.

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A total of 198 sera from stray cats was assayed against Toxoplasma gondii antigen by western blot. Out of 198 sera assayed, 26 sera (13.1%) showed typical blot patterns against T. gondii. When spotted by ELISA absorbance and indirect latex agglutination test (ILAT) titer, all 26 cases were distributed over the cut-off value of ELISA whereas 24 cases (92.3%) were in the positive range of 1:32 or higher and 2 cases in negative range by ILAT. Among western blot negative 172 sera, 162 cases were negative in both ILAT and ELISA while 10 cases were reactive falsely such that three cases were ILAT positive with 1:32 titer and 9 cases were ELISA positive (2 cases overlapped). These 10 cases reacted peculiarly without typical binding pattern in Western blot. Sandwich-ELISA was performed with monoclonal antibodies (mAbs) of Tg563 (30 kDa, SAG1), Tg505 (22 kDa, SAG2), Tg605 (43 kDa, SAG3), Tg556 (28 kDa, GRA2), Tg737 (32 kDa, GRA6), Tg695 (66 kDa, ROP2), Tg786 (42 kDa, ROP6), and Tg621 (32 kDa, anonymous but cytosolic) clone, respectively. All western blot-positive cases were in the positive range and negative cases in the negative range clearly. Among the 10 false reactive cases, 3 cases were in the positive range with one or more mAbs. All mAbs used in this study were confirmed to be specific to T. gondii infection as a standardized sandwich-ELISA to differentiate it from other pathogens.

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Upregulated expression of the cDNA fragment possibly related to the virulence of Acanthamoeba culbertsoni
Kyung-Il Im, Kwang-Min Park, Tai-Soon Yong, Yong-Pyo Hong, Tae-Eun Kim
Korean J Parasitol 1999;37(4):257-263.
Published online December 31, 1999
DOI: https://doi.org/10.3347/kjp.1999.37.4.257

Identification of the genes responsible for the recovery of virulence in brain-passaged Acanthamoeba culbertsoni was attempted via mRNA differential display-polymerase chain reaction (mRNA DD-PCR) analysis. In order to identify the regulatory changes in transcription of the virulence related genes by the brain passages, mRNA DD-PCR was performed which enabled the display of differentially transcribed mRNAs after the brain passages. Through mRNA DD-PCR analysis, 96 brain-passaged amoeba specific amplicons were observed and were screened to identify the amplicons that failed to amplify in the non-brain-passaged amoeba mRNAs. Out of the 96 brain-passaged amoeba specific amplicons, 12 turned out to be amplified only from the brain-passaged amoeba mRNAs by DNA slot blot hybridization. The clone, A289C, amplified with an arbitrary primer of UBC #289 and the oligo dT11-C primer, revealed the highest homology (49.8%) to the amino acid sequences of UPD-galactose lipid transferase of Erwinia amylovora, which is known to act as an important virulence factor. The deduced amino acid sequences of an insert DNA in clone A289C were also revealed to be similar to cpsD, which is the essential gene for the expression of type III capsule in group B streptococcus. Upregulated expression of clone A289C was verified by RNA slot blot hybridization. Similar hydrophobicity values were also observed between A289C (at residues 47-66) and the AmsG gene of E. amylovora (at residues 286-305: transmembrane domains). This result suggested that the insert of clone A289C might play the same function as galactosyl transferase controlled by the AmsG gene in E. amylovora.

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    Lizbeth Salazar-Villatoro, Bibiana Chávez-Munguía, Celia Esther Guevara-Estrada, Anel Lagunes-Guillén, Dolores Hernández-Martínez, Ismael Castelan-Ramírez, Maritza Omaña-Molina
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Two new genotypes of Plasmodium vivax circumsporozoite protein found in the Republic of Korea
Weon-Gyu Kho, Yeong-Hong Park, Joon-Yong Chung, Jong-Pil Kim, Sung-Tae Hong, Won-Ja Lee, Tong-Soo Kim, Jong-Soo Lee
Korean J Parasitol 1999;37(4):265-270.
Published online December 31, 1999
DOI: https://doi.org/10.3347/kjp.1999.37.4.265

The gene encoding Plasmodium vivax circumsporozoite protein (PvCSP) exhibits polymorphism in many geographical isolates. The present study was designed to investigate polymorphism in PvCSP gene of P. vivax isolates in Korea. Thirty isolates, obtained from indigenous cases in Yonchon-gun, Kyonggi-do in 1997, were subjected for sequencing and RFLP analysis of the repeat and post-repeat regions of PvCSP gene and two genotypes (SK-A and SK-B) were identified. The genotype of 19 isolates was SK-A and that of 11 isolates was SK-B. Although the number of 12-base repeats present in SK-A was three while two were found in a Chinese strain CH-5, the repeat sequence of SK-A was identical to that of CH-5 except for one base substitution. Compared with known data there was no identical isolates with SK-B, but the sequence of SK-B was similar to that of a North Korean (NK) isolate. These results indicate that two genotypes of PvCSP coexist in the present epidemic area of Korea and the present parasite may originate from East Asia. RFLP would be useful to classify genotypes of P. vivax population instead of gene sequencing.

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  • Exploring genetic polymorphisms among Plasmodium vivax isolates from the Thai-Myanmar borders using circumsporozoite protein (pvcsp) and ookinete surface protein (pvs25) encoding genes
    Bashir Abdirahman Guled, Kesara Na-Bangchang, Wanna Chaijaroenkul
    Parasitology Research.2024;[Epub]     CrossRef
  • Genetic diversity of pvcsp and pvs25 in Plasmodium vivax isolates in malaria-endemic areas in Asia, Africa, and America: A systematic review
    Abdirahman Guled Bashir, Chiajaroenkul Wanna, Na-Bangchang Kesara
    African Journal of Pharmacy and Pharmacology.2023; 17(5): 73.     CrossRef
  • Genetic Diversity of Plasmodium vivax Causing Epidemic Malaria in the Republic of Korea
    Young Yil Bahk, Jeonga Kim, Seong Kyu Ahn, Byoung-Kuk Na, Jong-Yil Chai, Tong-Soo Kim
    The Korean Journal of Parasitology.2018; 56(6): 545.     CrossRef
  • Population genetics structure of Plasmodium vivax circumsporozoite protein during the elimination process in low and unstable malaria transmission areas, southeast of Iran
    Samaneh Hemati Shabani, Sedigheh Zakeri, Akram Abouie Mehrizi, Yousef Mortazavi, Navid Dinparast Djadid
    Acta Tropica.2016; 160: 23.     CrossRef
  • Molecular genetic analysis of Plasmodium vivax isolates from Eastern and Central Sudan using pvcsp and pvmsp-3α genes as molecular markers
    Albadawi Abdelbagi Talha, Sekineh Pirahmadi, Akram Abouie Mehrizi, Navid Dinparast Djadid, Bakri Y.M. Nour, Sedigheh Zakeri
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  • Molecular epidemiology of Plasmodium vivax in Latin America: polymorphism and evolutionary relationships of the circumsporozoite gene
    Lilia González-Cerón, Jesus Martinez-Barnetche, Ciro Montero-Solís, Frida Santillán, Aida M Soto, Mario H Rodríguez, Benjamin J Espinosa, Octavio A Chávez
    Malaria Journal.2013;[Epub]     CrossRef
  • Microsatellite DNA Analysis Revealed a Drastic Genetic Change of Plasmodium vivax Population in the Republic of Korea During 2002 and 2003
    Moritoshi Iwagami, Seung-Young Hwang, So-Hee Kim, So-Jung Park, Ga-Young Lee, Emilie Louise Akiko Matsumoto-Takahashi, Weon-Gyu Kho, Shigeyuki Kano, Shan Lv
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  • Serological responses to a soluble recombinant chimeric Plasmodium vivax circumsporozoite protein in VK210 and VK247 population
    Yang Cheng, Daisuke Ito, Jetsumon Sattabongkot, Chae Seung Lim, Deok-Hoon Kong, Kwon-Soo Ha, Bo Wang, Takafumi Tsuboi, Eun-Taek Han
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  • Population Structure and Transmission Dynamics of Plasmodium vivax in the Republic of Korea Based on Microsatellite DNA Analysis
    Moritoshi Iwagami, Megumi Fukumoto, Seung-Young Hwang, So-Hee Kim, Weon-Gyu Kho, Shigeyuki Kano, Mehmet Ali Ozcel
    PLoS Neglected Tropical Diseases.2012; 6(4): e1592.     CrossRef
  • Trials for the co-expression of the merozoite surface protein-1 and circumsporozoite protein genes of Plasmodium vivax
    Choonghee Lee, Kyung Won Chung, Tong-Soo Kim, Kyung-Mi Choi, Yien Kyoung Choi, Nam-Jun Chung, Ho-Gun Rhie, Ho-Sa Lee, Sung-Jae Lee, Hyeong-Woo Lee
    Experimental Parasitology.2011; 129(3): 227.     CrossRef
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    Choonghee Lee, Hyung-Hwan Kim, Kyung Mi Choi, Kyung Won Chung, Yien Kyoung Choi, Mi Jung Jang, Tong-Soo Kim, Nam-Jun Chung, Ho-Gun Rhie, Ho-Sa Lee, Youngjoo Sohn, Hyuck Kim, Sung-Jae Lee, Hyeong-Woo Lee
    Malaria Journal.2011;[Epub]     CrossRef
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    Myriam Arévalo-Herrera, Sócrates Herrera, Miguel Ángel Hernández-Martínez, Ananías A. Escalante
    The American Journal of Tropical Medicine and Hygiene.2011; 84(2_Suppl): 51.     CrossRef
  • Genetic Characteristics of Polymorphic Antigenic Markers among Korean Isolates of Plasmodium vivax
    Seung-Young Hwang, So-Hee Kim, Weon-Gyu Kho
    The Korean Journal of Parasitology.2009; 47(Suppl): S51.     CrossRef
  • Molecular Genetic Characterization of the Merozoite Surface Protein 1 Gene of Plasmodium vivax from Reemerging Korean Isolates
    So-Hee Kim, Seung-Young Hwang, Jeong Hwan Shin, Chi-Sook Moon, Dong-Wook Kim, Weon-Gyu Kho
    Clinical and Vaccine Immunology.2009; 16(5): 733.     CrossRef
  • Reemergence of Malaria in Korea
    Weon-Gyu Kho
    Journal of the Korean Medical Association.2007; 50(11): 959.     CrossRef
  • A new polymerase chain reaction/restriction fragment length polymorphism protocol for Plasmodium vivax circumsporozoite protein genotype (VK210, VK247, and P. vivax-like) determination
    Renata Tomé Alves, Marinete Marins Póvoa, Ira F. Goldman, Carlos Eugênio Cavasini, Andréa Regina Baptista Rossit, Ricardo Luiz Dantas Machado
    Diagnostic Microbiology and Infectious Disease.2007; 59(4): 415.     CrossRef
  • Reemerging vivax malaria: changing patterns of annual incidence and control programs in the Republic of Korea
    Eun-Taek Han, Duk-Hyoung Lee, Ki-Dong Park, Won-Seok Seok, Young-Soo Kim, Takafumi Tsuboi, Eun-Hee Shin, Jong-Yil Chai
    The Korean Journal of Parasitology.2006; 44(4): 285.     CrossRef
  • Analysis of the Plasmodium vivax apical membrane antigen-1 gene from re-emerging Korean isolates
    Joon-Yong Chung, Eui-Hyun Chun, Jin-Ho Chun, Weon-Gyu Kho
    Parasitology Research.2003; 90(4): 325.     CrossRef
  • Detection of vivax sporozoites naturally infected in Anopheline mosquitoes from endemic areas of northern parts of Gyeonggi-do (province) in Korea
    Hyeong Woo Lee, E Hyun Shin, Shin Hyeong Cho, Hee Il Lee, Chung Lim Kim, Wook Gyo Lee, Sung Ung Moon, Jong Soo Lee, Wan Ja Lee, Tong Soo Kim
    The Korean Journal of Parasitology.2002; 40(2): 75.     CrossRef
  • Apical membrane antigen-1 (AMA-1) gene sequences of re-emerging Plasmodium vivax in South Korea
    Eun-Taek Han, Jae-Hwan Park, Eun-Hee Shin, Min-Ho Choi, Myoung-Don Oh, Jong-Yil Chai
    The Korean Journal of Parasitology.2002; 40(3): 157.     CrossRef
  • Analysis of polymorphic region of GAM-1 gene in Plasmodium vivax Korean isolates
    Weon-Gyu Kho, Joon-Yong Chung, Ui-Wook Hwang, Jin-Ho Chun, Yeong-Hong Park, Woo-Chul Chung
    The Korean Journal of Parasitology.2001; 39(4): 313.     CrossRef
  • Incidence patterns of vivax malaria in civilians residing in a high-risk county of Kyonggi-do (Province), Republic of Korea
    Jung Ju Moon, Seung-Yull Cho
    The Korean Journal of Parasitology.2001; 39(4): 293.     CrossRef
  • Analysis of polymorphic regions of Plasmodium vivax Duffy binding protein of Korean isolates
    Weon-Gyu Kho, Joon-Yong Chung, Eun-Jeong Sim, Dong-Wook Kim, Woo-Chul Chung
    The Korean Journal of Parasitology.2001; 39(2): 143.     CrossRef
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Karyotypes of Pneumocystis carinii derived from several mammals
Sang Rock Cho, Yun-Gyu Park, Hyung Nam Moon, Soon-Hyung Lee, Sung-Tae Hong
Korean J Parasitol 1999;37(4):271-275.
Published online December 31, 1999
DOI: https://doi.org/10.3347/kjp.1999.37.4.271

Pneumocystis carinii is the most important opportunistic pathogen of humans in the world. Pneumocystis carinii is experimentally detected in the lungs of rats, mice, rabbits, and monkeys, however, the organisms from different mammals are identical in microscopic morphology. The present study tried to find out more mammalian hosts of P. carinii and also to differentiate the organisms from different mammals by karyotyping. Rats, mice, hamsters, rabbits, cats, and dogs were successfully infected by P. carinii, but guinea pigs and pigs were not. Karyotype of P. carinii from rabbits showed similar size range of chromosomes with that of the prototype, but in different pattern. The patterns from cats and dogs were also different from that of rats. The present study confirms that cats and dogs are infected by P. carinii and at least total three karyotype strains of P. carinii are proven in Korea.

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    Diana Riebold, Marie Mahnkopf, Kristina Wicht, Cristina Zubiria-Barrera, Jan Heise, Marcus Frank, Daniel Misch, Torsten Bauer, Hartmut Stocker, Hortense Slevogt
    Journal of Fungi.2023; 9(9): 903.     CrossRef
  • Respiratory Diseases in Guinea Pigs, Chinchillas and Degus
    María Ardiaca García, Andrés Montesinos Barceló, Cristina Bonvehí Nadeu, Vladimír Jekl
    Veterinary Clinics of North America: Exotic Animal Practice.2021; 24(2): 419.     CrossRef
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    Patrizia Danesi, Michela Corrò, Christian Falcaro, Antonio Carminato, Tommaso Furlanello, Monia Cocchi, Mark B Krockenberger, Wieland Meyer, Gioia Capelli, Richard Malik
    Medical Mycology.2018;[Epub]     CrossRef
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    Magali Chabé, Cécile-Marie Aliouat-Denis, Laurence Delhaes, El Moukhtar Aliouat, Eric Viscogliosi, Eduardo Dei-Cas
    FEMS Yeast Research.2011; 11(1): 2.     CrossRef
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    Jae-Seok Kim, Yong-Kyun Kim, Ji Young Park, Eun Kyung Mo, Han Sung Kim, Wonkeun Song, Hyoun Chan Cho, Kyu Man Lee
    Chonnam Medical Journal.2008; 44(2): 82.     CrossRef
  • Pneumocystis species, co-evolution and pathogenic power
    Cécile-Marie Aliouat-Denis, Magali Chabé, Christine Demanche, El Moukhtar Aliouat, Eric Viscogliosi, Jacques Guillot, Laurence Delhaes, Eduardo Dei-Cas
    Infection, Genetics and Evolution.2008; 8(5): 708.     CrossRef
  • Pneumocystis
    James R. Stringer
    International Journal of Medical Microbiology.2002; 292(5-6): 391.     CrossRef
  • Genetic heterogeneity of Pneumocystis carinii from rats of several regions and strains
    Byung-Suk Chung, Yun-Kyu Pars, Sun Huh, Jae-Ran Yu, Jin Kim, Xiaohua Shi, Sang Rock Cho, Soon-Hyung Lee, Sung-Tae Hong
    The Korean Journal of Parasitology.2000; 38(3): 151.     CrossRef
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Expression of major piroplasm protein (p33) of Theileria sergenti (Korean isolate) and its immunogenicity in guinea pigs
Seung-Won Kang, Chang-Hee Kweon, Eun-Jin Choi, Yong-Dhuk Yoon
Korean J Parasitol 1999;37(4):277-283.
Published online December 31, 1999
DOI: https://doi.org/10.3347/kjp.1999.37.4.277

To investigate the development of a subunit vaccine against theileriosis in cattle, the DNA fragments encoding piroplasm surface protein (p33) of Theileria sergenti of a Korean isolate were expressed in baculoviruses. The expressed p33 was characterized by indirect fluorescent antibody (IFA) and western blotting analysis. The expression of p33 was mainly detected on the surface of infected Sf21 cells by IFA. The immunoblotting analysis revealed the presence of a same molecular weight protein band of p33. The antigenicity of expressed polypeptide was further examined through the inoculation of a guinea pig. The sera of guinea pigs immunized with p33 expressed cell lysate showed similar fluorescent antibody patterns and reacted with the same molecular weight protein of T. sergenti in immunoblotting analysis, thus indicating that this protein can be a promising candidate for a subunit vaccine in the future.

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  • Adjuvant effect of bovine heat shock protein 70 on piroplasm surface protein, p33, of Theileria sergenti
    Wooseog Jeong, Chang Hee Kweon, Seung Won Kang, Hyang Sim Lee, Yingtian Xu, Cheng Lu, Shoufa Zhang, Vishvanath Nene
    Biologicals.2009; 37(5): 282.     CrossRef
  • SEROLOGICAL INVESTIGATION OF THEILERIA SERGENTI USING LATEX AGGLUTINATION TEST IN SOUTH KOREA
    Wooseog Jeong, Chang Hee Kweon, Jong Man Kim, Hwan Jang, Sang Gi Paik
    Journal of Parasitology.2005; 91(1): 164.     CrossRef
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Brief Communications
Changes of splenocyte IFN-γ mRNA synthesis in rats infected with Paragonimus westermani
Jun Kyong Cho, Hye Soo Kwon, Kyoung Hwan Joo, Joon Sang Lee, Sung-Weon Cho
Korean J Parasitol 1999;37(4):285-287.
Published online December 31, 1999
DOI: https://doi.org/10.3347/kjp.1999.37.4.285

Changes in the expression level of splenocyte IFN-γ mRNA of Sprague-Dawley (SD) rats infected with Paragonimus westermani were analyzed by competitive reverse transcription-polymerase chain reaction (RT-PCR) followed by southern blot. The template RNA was extracted from the splenocytes of rats infected with 20 metacercariae of P. westermani. The products of competitive RT-PCR were subjected to southern blot and enhanced chemiluminescence (ECL), and analyzed with a densitometer. In comparison with that of uninfected control rat splenocytes (value of 1), the levels of mRNA expression of IFN-γ had changed to 0.747 at 1 week post infection (PI), 0.00175 at 2 week PI, 0.0217 at 3 week PI, 0.194 at 4 week PI and then to 0.537 at 5 week PI. The level at 7 week PI had returned to 1.25, comparable with that of uninfected rats. These results show that, when infected with P. westermani, the levels of IFN-γ mRNA of SD rat splenocytes were remarkably reduced by more than 500 times at 2 week PI and restored to normal level at 7 week PI.

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  • Adjuvant effect of Korean mistletoe lectin on mucosal immunity induction following intranasal immunization with hemagglutinin antigen
    Jin Hyuk Jung, Young Hoon Kim, Tae Jun Song, Hyosun An, Kyu Dae Kim, In Bo Kim, Taek Joon Yoon, Jong Bae Kim
    Food Science and Biotechnology.2011; 20(3): 629.     CrossRef
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Towards developing a diagnostic regimen for the treatment follow-up of Trypanosoma brucei gambiense
Peter A. Mbati, Kazuko Hirumi, Noboru Inoue, Nanituma H. Situakibanza, Hiroyuki Hirumi
Korean J Parasitol 1999;37(4):289-292.
Published online December 31, 1999
DOI: https://doi.org/10.3347/kjp.1999.37.4.289

BALB/c mice infected with a high virulent strain of Trypanosoma brucei gambiense IL3707 were treated intraperitoneally (ip) with either Melarsoprol (Mel-B) or PSG(+) buffer as controls. The mice were subsequently monitored regularly for parasites by direct microscopic examination of their tail blood or buffy coat and by polymerase chain reaction (PCR). Mel-B was found to be an effective drug for treatment against T.b. gambiense because at the end of the first treatment schedule, all treated mice were negative for parasites even by PCR, while all the control animals were positive. Three of the five Mel-B treated mice, while parasitologically negative, were PCR positive between 53 and 80 days post infection (DPI), indicating that they still harbored an infection. All treated mice were subsequently negative for parasites even by PCR at 88 DPI. A combination of conventional microscopic examination and PCR offers a good prediction of cure following treatment of trypanosomosis.

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  • Diagnostic Accuracy of PCR in gambiense Sleeping Sickness Diagnosis, Staging and Post-Treatment Follow-Up: A 2-year Longitudinal Study
    Stijn Deborggraeve, Veerle Lejon, Rosine Ali Ekangu, Dieudonné Mumba Ngoyi, Patient Pati Pyana, Médard Ilunga, Jean Pierre Mulunda, Philippe Büscher, Serap Aksoy
    PLoS Neglected Tropical Diseases.2011; 5(2): e972.     CrossRef
  • Novel Markers for Treatment Outcome in Late‐StageTrypanosoma brucei gambienseTrypanosomiasis
    Veerle Lejon, Isabelle Roger, Dieudonné Mumba Ngoyi, Joris Menten, Jo Robays, Francois X. N’Siesi, Sylvie Bisser, Marleen Boelaert, Philippe Büscher
    Clinical Infectious Diseases.2008; 47(1): 15.     CrossRef
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