1.Macrophages, myofibroblasts and mast cells in a rat liver infected with Capillaria hepatica.
Won Il JEONG ; Sun Hee DO ; Il Hwa HONG ; Ae Ri JI ; Jin Kyu PARK ; Mi Ran KI ; Seung Chun PARK ; Kyu Shik JEONG
Journal of Veterinary Science 2008;9(2):211-213
We trapped a rat (Rattus norvegicus) infected with Capillaria hepatica. At necropsy, grossly yellowish-white nodules (2-3 mm in diameter) were noted to be scattered on the liver's surface. Microscopically, granulomatous and fibrotic nodules that contained the eggs and/or adult worms of Capillaria hepatica were detected in the liver. Septal fibrosis was diffusely formed throughout the liver. There were a number of ED1-positive macrophages located in the sinusoids of the pseudolobules. On the double staining, myofibroblasts and mast cells were generally observed within the fibrous septa with the mast cells in close proximity to the myofibroblasts. We suggest that the interactions between macrophages, myofibroblasts and mast cells play a role in the septal fibrosis observed in rats infected by Capillaria hepatica.
Animals
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*Capillaria
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Enoplida Infections/immunology/parasitology/*veterinary
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Fibroblasts/immunology
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Liver/parasitology/pathology
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Macrophages/immunology
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Mast Cells/immunology
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Rats
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Rodent Diseases/*immunology/*parasitology/pathology
2.Study on the situation of plague in Junggar Basin of China.
Yu-Jiang ZHANG ; Xiang DAI ; Abulimiti ; Wei JIANG ; Abulikemu ; Xin-Hui WANG ; Burenmingde ; Rena ; Bing LI ; Gang LEI ; Wei-Wei MENG ; Muhetaer ; Xiao-Bing ZHANG ; Qi-Guo WANG ; Tao LUO ; Rong GUO ; Zhong WANG ; Jian-Guo TANG ; Cheng-Quan LIU ; Azati ; Rui-Yu YE ; Xin YU ; Han-Li CAO
Chinese Journal of Epidemiology 2008;29(2):136-144
OBJECTIVETo understand the distribution, fauna, population structure of host animals and their parasitic fleas as well as popular dynamic of animal plague of natural plague foci in Junggar Basin.
METHODSSample materials and data of animals and vector insects were collected using ecological methods and the population structures were analyzed statistically. F1 antibody of Yersinia pestis in rodents' serum and organ suspension was detected by means of IHA while the pathogen of Y. pestis in rodents and vector insects was detected by means of aetiological detections and the isolated Y. pestis was detected using biochemical methods.
RESULTSThe small mammals which were found in Junggar Basin belonged to 17 species of 11 genera 7 families. Of them, 13 species of rodents were included whose parasitic fleas belonged to 19 species of 10 genera 8 families. The average coverage of Rhombomys opimus hole-community was 22.5% in Junggar Basin with the average density of R. opimus hole-community was 15.9/hm2 and the average rate of habitat of the hole-community was 70.2%. In the R. opimus community, the average density of rodents was 3.1/hole-community, and 34.4/hm2 in the nature plague foci. In the population structure of the hole-community of R. opimus, R. opimus accounted for 72.9% in the total captured rodents, Meriones meridianus was 24.5% while the others were 2.6%. In the nocturnal community of rodents, M. meridianus accounted for 64.0% in total captured rodents, Dipus sagitta was 15.1%, M. erythrourns was 7.5% and the others were 13.4%. In the rodents community of Junggar Basin, the rate of R. opimus with fleas was 84.9%, which was the highest, followed by M. tamariscinus, Euchoreutes naso and M. erythrourns, with the rates as 71.4%, 66.7% and 62.7% respectively. The rate of M. meridianus with fleas was 38.3%. There were 16 species of parasitic fleas in R. opimus, with the total flea index as 8.58 and the dominant species was Xenopsylla skrjabini. There were 17 and 16 kinds of fleas in M. erythrourns and M. meridianus respectively with the total flea index were 1.59 and 1.15, with dominant fleas were Nosopsyllus laeviceps and X. skrjabini. The serum and organ suspension of 3179 rodents which belonged to 12 species were detected by means of IHA, of them 174 samples were positive and the positive rate was 5.5%. There were 1356 samples of R. opimus in these materials, and 164 were positive, accounted for 12.1%. The samples of M. meridianus were 1255, with 9 positive, accounted for 0.7%. The samples of D. sagitta were 116 with 1 positive and the rate was 0.9%. The samples of other rodents were 452 but were all negative. There were in total 2975 organs collected from rodents, when detected by methods of isolated of Y. pestis. 15 strains of Y. pestis were isolated from 1243 R. opimus, and 2 strains isolated from 1230 M. meridianus. A total number of 11 647 fleas from rodents were detected by methods of isolated of Y. pestis in which 1 strain of Y. pestis was isolated from 4713 X. skrjabini, and 6 were isolated from 2101 Xenopsylla minax, 1 from 328 Xenopsylla conformis conformis and 1 from 250 Echidnophaga oschanini. Among the other 4255 fleas, none was isolated. The biochemical properties of these Y. pestis which isolated from Junggar Basin were positive of Maltose, Ejiao sugar and Glycerol, and negative of Rhamnose and Nitrogen, which were all strongly poisonous to mouse.
CONCLUSIONThe natural plague foci in Junggar Basin spread all over the whole Junggar Basin. There were animal plague cases found in 12 counties (cites) while Karamy, Bole, Jimusaer and Qitai were confirmed as plague foci counties (cities). Animals and vector insects of the foci were complicated but the ecological system was stable. R. opimus was recognized as the dominant host animal and its biochemical type belonged to the Middle Ages, suggesting that the foci was a new type of natural plague foci.
Animals ; China ; epidemiology ; Gerbillinae ; microbiology ; Mice ; Plague ; epidemiology ; microbiology ; Rodent Diseases ; epidemiology ; microbiology ; Yersinia pestis ; immunology ; pathogenicity
3.Pro-inflammatory Cytokine Expression of Spleen Dendritic Cells in Mouse Toxoplasmosis.
Ho Woo NAM ; Hye Jin AHN ; Hyun Jong YANG
The Korean Journal of Parasitology 2011;49(2):109-114
Dendritic cells have been known as a member of strong innate immune cells against infectious organelles. In this study, we evaluated the cytokine expression of splenic dendritic cells in chronic mouse toxoplasmosis by tissue cyst-forming Me49 strain and demonstrated the distribution of lymphoid dendritic cells by fluorescence-activated cell sorter (FACS). Pro-inflammatory cytokines, such as IL-1alpha, IL-1beta, IL-6, and IL-10 increased rapidly at week 1 post-infection (PI) and peaked at week 3 PI. Serum IL-10 level followed the similar patterns. FACS analysis showed that the number of CD8alpha+/CD11c+ splenic dendritic cells increased at week 1 and peaked at week 3 PI. In conclusion, mouse splenic dendritic cells showed early and rapid cytokine changes and may have important protective roles in early phases of murine toxoplasmosis.
Animals
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Antigens, CD11c/analysis
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Antigens, CD8/analysis
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Cytokines/*blood/*secretion
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Dendritic Cells/chemistry/*immunology
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Disease Models, Animal
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Flow Cytometry
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Mice
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Mice, Inbred BALB C
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Rodent Diseases/immunology
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Spleen/*immunology
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Time Factors
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Toxoplasmosis, Animal/*immunology
4.Expression of TNF-alpha and IL-1beta in Splenic Dendritic Cells and Their Serum Levels in Mouse Sparganosis.
The Korean Journal of Parasitology 2011;49(2):191-194
Sparganosis is a tissue invading helminthiasis infecting intermediate hosts, including humans. Strong immune responses are expected to occur in early phases of infection. Thus, we investigated cytokine expressions in splenic dendritic cells and in sera after experimental infection of mice. In splenic dendritic cells, TNF-alpha and IL-1beta expression peaked at week 1 and week 3 post-infection (PI), respectively, and also early phase (week 2 PI) depressed cytokine expression was noticed. Serum IL-1beta concentration increased significantly at week 2 PI and peaked at week 6 PI, and that of TNF-alpha peaked at week 6 PI. These results showed that pro-inflammatory cytokines, TNF-alpha and IL-1beta, are chronologically regulated in mouse sparganosis.
Animals
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Dendritic Cells/*immunology
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Disease Models, Animal
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Interleukin-1beta/*blood/*secretion
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Mice
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Mice, Inbred BALB C
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Rodent Diseases/immunology
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Serum/chemistry
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Sparganosis/*immunology
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Spleen/*immunology
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Tumor Necrosis Factor-alpha/*blood/*secretion
5.Immune Responses of Mice Intraduodenally Infected with Toxoplasma gondii KI-1 Tachyzoites.
Eun Hee SHIN ; Yeoun Sook CHUN ; Won Hee KIM ; Jae Lip KIM ; Kyoung Ho PYO ; Jong Yil CHAI
The Korean Journal of Parasitology 2011;49(2):115-123
Toxoplasma gondii Korean isolate (KI-1) tachyzoites were inoculated intraduodenally to BALB/c mice using a silicon tube, and the course of infection and immune responses of mice were studied. Whereas control mice, that were infected intraperitoneally, died within day 7 post-infection (PI), the intraduodenally infected mice survived until day 9 PI (infection with 1x10(5) tachyzoites) or day 11 PI (with 1x10(6) tachyzoites). Based on histopathologic (Giemsa stain) and PCR (B1 gene) studies, it was suggested that tachyzoites, after entering the small intestine, invaded into endothelial cells, divided there, and propagated to other organs. PCR appeared to be more sensitive than histopathology to detect infected organs and tissues. The organisms spread over multiple organs by day 6 PI. However, proliferative responses of splenocytes and mesenteric lymph node (MLN) cells in response to con A or Toxoplasma lysate antigen decreased significantly, suggesting immunosuppression. Splenic CD4+ and CD8+ T-lymphocytes showed decreases in number until day 9 PI, whereas IFN-gamma and IL-10 decreased slightly at day 6 PI and returned to normal levels by day 9 PI. No TNF-alpha was detected throughout the experimental period. The results showed that intraduodenal infection with KI-1 tachyzoites was successful but did not elicit significant mucosal immunity in mice and allowed dissemination of T. gondii organisms to systemic organs. The immunosuppression of mice included reduced lymphoproliferative responses to splenocytes and MLN cells to mitogen and low production of cytokines, such as IFN-gamma, TNF-alpha, and IL-10, in response to T. gondii infection.
Animals
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Cell Proliferation
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Cytokines/secretion
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Disease Models, Animal
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Duodenum/immunology/parasitology/pathology
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Endothelial Cells/parasitology
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Histocytochemistry
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Immune Tolerance
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Lymph Nodes/immunology
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Mice
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Mice, Inbred BALB C
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Polymerase Chain Reaction
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Rodent Diseases/immunology/parasitology/pathology
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T-Lymphocyte Subsets/immunology
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Toxoplasma/*immunology/pathogenicity
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Toxoplasmosis, Animal/*immunology/parasitology/pathology
6.Molecular cloning, characterization and expression analysis of woodchuck retinoic acid-inducible gene I.
Qi YAN ; Qin LIU ; Meng-Meng LI ; Fang-Hui LI ; Bin ZHU ; Jun-Zhong WANG ; Yin-Ping LU ; Jia LIU ; Jun WU ; Xin ZHENG ; Meng-Ji LU ; Bao-Ju WANG ; Dong-Liang YANG
Journal of Huazhong University of Science and Technology (Medical Sciences) 2016;36(3):335-343
Cytosolic retinoic acid-inducible gene I (RIG-I) is an important innate immune RNA sensor and can induce antiviral cytokines, e.g., interferon-β (IFN-β). Innate immune response to hepatitis B virus (HBV) plays a pivotal role in viral clearance and persistence. However, knowledge of the role that RIG-I plays in HBV infection is limited. The woodchuck is a valuable model for studying HBV infection. To characterize the molecular basis of woodchuck RIG-I (wRIG-I), we analyzed the complete coding sequences (CDSs) of wRIG-I, containing 2778 base pairs that encode 925 amino acids. The deduced wRIG-I protein was 106.847 kD with a theoretical isoelectric point (pI) of 6.07, and contained three important functional structures [caspase activation and recruitment domains (CARDs), DExD/H-box helicases, and a repressor domain (RD)]. In woodchuck fibroblastoma cell line (WH12/6), wRIG-I-targeted small interfering RNA (siRNA) down-regulated RIG-I and its downstrean effector-IFN-β transcripts under RIG-I' ligand, 5'-ppp double stranded RNA (dsRNA) stimulation. We also measured mRNA levels of wRIG-I in different tissues from healthy woodchucks and in the livers from woodchuck hepatitis virus (WHV)-infected woodchucks. The basal expression levels of wRIG-I were abundant in the kidney and liver. Importantly, wRIG-I was significantly up-regulated in acutely infected woodchuck livers, suggesting that RIG-I might be involved in WHV infection. These results may characterize RIG-I in the woodchuck model, providing a strong basis for further study on RIG-I-mediated innate immunity in HBV infection.
Animals
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Cell Line, Tumor
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Cloning, Molecular
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DEAD Box Protein 58
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antagonists & inhibitors
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genetics
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immunology
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Fibroblasts
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immunology
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pathology
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Gene Expression
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Hepatitis B
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genetics
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immunology
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pathology
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veterinary
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Hepatitis B Virus, Woodchuck
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Immunity, Innate
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Interferon-beta
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genetics
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immunology
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Isoelectric Point
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Kidney
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immunology
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pathology
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virology
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Liver
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immunology
;
pathology
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virology
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Marmota
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genetics
;
immunology
;
virology
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Open Reading Frames
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Protein Domains
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RNA, Double-Stranded
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RNA, Small Interfering
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genetics
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metabolism
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Rodent Diseases
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genetics
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immunology
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pathology
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virology
7.Investigation on hantaviruses infection in rodents from free markets in Beijing areas.
Jia-fu JIANG ; Xiao-ming WU ; Ri-ming WANG ; Shu-qing ZUO ; Wei-cai XU ; Tian-yu GUO ; Li-quan CHEN ; Wu-chun CAO
Chinese Journal of Epidemiology 2006;27(2):145-149
OBJECTIVEIn order to find out the factors related to hemorrhagic fever with renal syndrome (HFRS) infection, and to evaluate the probability of ecdemic hantaviruses (HV) infection in rodents in Beijing areas.
METHODSRodents were collected in a large-scale railway station and a produce market with 'trap nights' method from April to May, 2004. The IgG reacting sera to HV antigen were detected using ELISA. The partial M and S segment of HV from captured rodent lung samples were amplified with RT-PCR. The PCR products were purified and sequenced. BLAST program was then used to perform on nucleotide pairwise alignment with all available sequence in GenBank. The alignment of the multiply nucleotide and the deduced amino acid sequences, together with phylogenetic analysis were completed with DNASTAR software.
RESULTSThe average population density was 3.49% (24/690). The overall seroprevalence of HV infection was 8.3% (2/24). RT-PCR positive rates were 8.3% (2/24). The nucleotide sequences of 356 bp region (1958 - 2313) of M segment obtained from 2 samples were all identified to Seoul virus (SEOV), with 7.6% heterogeneity. The dc501 strain from railway station was closely related to SD227 and Hebei4 from Shandong and Hebei provinces respectively. BjFT01 strain from the farm product market had more special nucleotide transitional mutations than other known SEOV from Beijing in GenBank. This strain, together with known HN71 from Hainan province, K24-E7 from Zhejiang province, L99 from Jiangxi province and R22 from Henan province, represented a monophylogentic linkage.
CONCLUSIONThe higher HV prevalence of rodents in transportation center was the potential and important risk for HFRS epidemic in Beijing. The increasing prevalence of M. musculus should call for attention. It was possible that SEOV in Beijing was imported by infected rodents through vehicles from other provinces.
Animals ; Antigens, Viral ; immunology ; China ; epidemiology ; Enzyme-Linked Immunosorbent Assay ; Hantavirus ; classification ; genetics ; isolation & purification ; Hantavirus Infections ; epidemiology ; immunology ; Hemorrhagic Fever with Renal Syndrome ; epidemiology ; Immunoglobulin G ; blood ; Lung ; virology ; Phylogeny ; Reverse Transcriptase Polymerase Chain Reaction ; Rodent Diseases ; epidemiology ; virology ; Rodentia ; Seroepidemiologic Studies
8.Monthly Occurrence of Vectors and Reservoir Rodents of Scrub Typhus in an Endemic Area of Jeollanam-do, Korea.
Seung Hyun LEE ; Young Sun LEE ; In Yong LEE ; Jae Won LIM ; Hee Kwan SHIN ; Jae Ran YU ; Seobo SIM
The Korean Journal of Parasitology 2012;50(4):327-331
Monthly surveys were conducted to investigate the occurrence of chigger mites and seroprevalence of scrub typhus among small mammals in Jeollanam-do, the southwestern part of Korea, from November 2006 through October 2007. Fifty-eight small mammals, including 57 Apodemus agrarius (98.3%) and 1 Crocidura lasiura (1.7%), were captured, and a total of 4,675 chigger mites representing 4 genera and 8 species were collected from them. The chigger infestation rate among small mammals was 69.0%. The most predominant species in A. agrarius was Leptotrombidium scutellare (54.0%), followed by Leptotrombidium pallidum (39.4%), Leptotrombidium orientale (4.4%), Leptotrombidium palpale (1.1%), Neotrombicula tamiyai (0.6%), Eushoengastia koreaensis (0.3%), Neotrombicula gardellai (0.3%), and Cheladonta ikaoensis (<0.1%). The chigger index of A. agrarius was the highest in October (740.0), followed by November (242.0), September (134.6), March (98.3), February (38.2), January (35.3), December (34.5), April (30.8), and May (1.7). The average antibody positive rate of scrub typhus in wild rodents was 50.0%. The seropositive rates were high in October (100.0%) and November (83.3%), whereas those in other months were relatively low (28.6-57.1%). The chigger index of L. scutellare rapidly increased in September to form an acuminate peak in October, followed by a gradual decline. These results suggest that the outbreak of scrub typhus in the southwestern part of Korean peninsula is mostly due to L. scutellare.
Animals
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Antibodies, Bacterial/blood
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Antibody Specificity
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Arachnid Vectors/*microbiology
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*Disease Reservoirs
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Humans
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Murinae/parasitology
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Orientia tsutsugamushi/*immunology
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Population Dynamics
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Public Health Surveillance
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Republic of Korea/epidemiology
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Rodent Diseases/parasitology/transmission
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Scrub Typhus/epidemiology/*transmission
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Seasons
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Seroepidemiologic Studies
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Shrews/parasitology
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Species Specificity
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Trombiculiasis/parasitology/veterinary
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Trombiculidae/*microbiology