2.Eco-geographic landscapes of natural plague foci in China III. Biological characteristics of major DFR/MLVA-based genotypes of Yersinia pestis, China.
Xi-ye FANG ; Dong-sheng ZHOU ; Yu-jun CUI ; Yan-jun LI ; Qi-yong LIU ; Lei XU ; Rui-fu YANG
Chinese Journal of Epidemiology 2012;33(5):536-539
Animals
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China
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Genotype
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Plague
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genetics
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microbiology
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Yersinia pestis
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genetics
3.Study on vector ability of Nosopsyllus wualis leizhouensis in the transmission of plague.
Han-biao OU ; Rong-xuan SHEN ; Hai MAI ; Guang-xiang DAI ; Man-qing ZHANG ; Hua-yuan YANG ; Yu-lian LI ; Min ZENG ; Xiang-ming YU
Chinese Journal of Epidemiology 2003;24(6):487-490
OBJECTIVETo find out the vector ability and function of Nosopsyllus wualis leizhouensis in the transmitting plague.
METHODSIn T: 19 degrees C +/- 1 degrees C, RH: 85% +/- 5%, data regarding the vector ability as cluster spreading, single flea spreading, single flea transmitting plague to single animal, formative bacterial embolus and infection fleas life-span through experiments was gathered.
RESULTSThe rate of infection on fleas was 94.64%, with 100% transmission rate of colony to spread, and 30% from single flea spreading to single animal. In the experiment of single flea transmission, all of the 388 rattus loseas were bitten by the fleas with bacterial, but only 9 animals were characteristically infected with the transmission potential, vector efficiency, survival potential of embolus, vector index as 0.360, 0.257, 0.868 and 0.223 respectively. The mean survive days of infected flea feed with blood were 17.58 (1 - 58), and the mean survive days of hunger infected flea were 7.25 (1 - 16). Formative bacterial embolus days were 8.80 (2 - 16) and the rate of embolus flea was 78.12%.
CONCLUSIONNosopsyllus wualis leizhouensis could serve as vector and important in the mode of plague transmittion.
Animals ; Female ; Insect Vectors ; microbiology ; Male ; Plague ; transmission ; Rats ; Siphonaptera ; microbiology
4.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
6.The epidemiology and etiology research of Tibetan sheep plague in Qinghai plateau.
Baiqing WEI ; Haoming XIONG ; Xiaoyan YANG ; Yonghai YANG ; Meiying QI ; Juan JIN ; Youquan XIN ; Xiang LI ; Hanqing YANG ; Xiumin HAN ; Ruixia DAI ; Email: DRX200907@163.COM.
Chinese Journal of Epidemiology 2015;36(3):271-274
OBJECTIVETo identify the epidemiology and etiology characteristics of Tibetan sheep plague in Qinghai plateau.
METHODSThe background materials of Qinghai Tibetan sheep plague found during 1975 to 2009 were summarized, the regional, time and interpersonal distribution, infection routes, ecological factors for the spread were used to analyze; followed by choosing 14 Yersinia pestis strains isolated from such sheep for biochemical test, toxicity test, virulence factors identification, plasmid analysis, and DFR genotype.
RESULTSFrom 1975 to 2009, 14 Yersinia pestis strains were isolated from Tibetan sheep in Qinghai province. Tibetan sheep, as the infection source, had caused 10 cases of human plague, 25 plague patients, and 13 cases of death. All of the initial cases were infected due to eating Tibetan sheep died of plague; followed by cases due to contact of plague patients, while all the initial cases were bubonic plague. Cases of bubonic plague developed into secondary pneumonic plague and septicemia plague were most popular and with high mortality. Most of the Tibetan sheep plague and human plague occurred in Gannan ecological zone in southern Gansu province, which was closely related to its unique ecological and geographical landscape. Tibetan sheep plague coincided with human plague caused by Tibetan sheep, especially noteworthy was that November (a time for marmots to start their dormancy) witnesses the number of Yersinia pestis strains isolated from Tibetan sheep and human plague cases caused by Tibetan sheep. This constituted the underlying cause that the epidemic time of Tibetan sheep plague lags obviously behind that of the Marmot plague. It was confirmed in the study that all the 14 strains were of Qinghai-Tibet Plateau ecotype, with virulence factors evaluation and toxicity test demonstrating strains as velogenic. As found in the (Different Region) DFR genotyping, the strains isolated from Yushu county and Zhiduo county were genomovar 5, the two strain isolated from Nangqian county were genomovar 5 and genomovar 7, while those isolated Delingha region were genomovar 8.
CONCLUSIONTibetan sheep were vulnerable to plague infection, hence causing human plague as the infectious source. The Yersinia pestis strains isolated from Tibetan sheep plague carried pathogen characteristics of Qinghai-Tibet plateau plague, developing many new characteristics of such plague.
Animals ; Ecology ; Genotype ; Geography ; Humans ; Marmota ; Plague ; epidemiology ; veterinary ; Plasmids ; Sheep ; microbiology ; Tibet ; epidemiology ; Yersinia pestis
7.Sources of infection on human plague in Qinghai province.
Cunxiang LI ; Baiqing WEI ; Haoming XIONG ; Meiying QI ; Xiaoyan YANG ; Youquan XIN ; Rongjie WEI ; Juan JIN ; Ruixia DAI
Chinese Journal of Epidemiology 2014;35(2):178-181
OBJECTIVETo study the biological and genetic characteristics of 119 strains of Yersinia (Y.) pestis isolated from plague patients in Qinghai province, from 1958-2012.
METHODSBoth regular methods and different region(DFR)molecular typing techniques were used to study the epidemiological characteristics on 119 strains of Y. pesticin Qinghai during 1958-2012. Sources of Y. pestis from two outbreaks, in Nangqian county in 2004 and in Xinghai county in 2009,Qinghai province were also analyzed.
RESULTS105 strains of Y. pestis were identified as Qinghai-Tibet Plateau Ecotype while the other 6 strains as Qilian Mountains Ecotype. 84.03% (100/119) of the tested strains carried 4 virulence factors F1(+), Pst I(+), VW(+) and Pgm(+)). 97.30% (72/74) of the tested strains showed high virulence. Strains that carrying 52×10(6), 65×10(6), 92×10(6) plasmids were distributed in Hainan, Haibei, Haixi,Yushu,Guoluo, Huangnan and Huangyuan counties. Genomovar 5 and 8 were the main gene types that circling around Qinghai Lake. Genomovar 10 was found in strains of Y. pesticin Nangqian county while Genomovar 8 was found in the strains isolated from human plague patient during the epidemics in Xinghai county in Qinghai.
CONCLUSIONData from biological and genetic analyses on the epidemics of human plague in Nangqian county in 2004 and in Xinghai county in 2009 demonstrated that methods as DFR genotyping and virulence factors profiles, as well as plasmids profiles were powerful tools in confirming the human plague epidemics and sources of infection.
China ; epidemiology ; Genotype ; Humans ; Plague ; epidemiology ; microbiology ; Yersinia pestis ; genetics ; isolation & purification
8.Formation and regulation of Yersinia biofilms.
Protein & Cell 2011;2(3):173-179
Flea-borne transmission is a recent evolutionary adaptation that distinguishes the deadly Yersinia pestis from its progenitor Y. Pseudotuberculosis, a mild pathogen transmitted via the food-borne route. Y. Pestis synthesizes biofilms in the flea gut, which is important for fleaborne transmission. Yersinia biofilms are bacterial colonies surrounded by extracellular matrix primarily containing a homopolymer of N-acetyl-D-glucosamine that are synthesized by a set of specific enzymes. Yersinia biofilm production is tightly regulated at both transcriptional and post-transcriptional levels. All the known structural genes responsible for biofilm production are harbored in both Y. Pseudotuberculosis and Y. Pestis, but Y. Pestis has evolved changes in the regulation of biofilm development, thereby acquiring efficient arthropod-borne transmission.
Animals
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Biofilms
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Caenorhabditis elegans
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physiology
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Humans
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Plague
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transmission
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Siphonaptera
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microbiology
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Transcription, Genetic
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Yersinia
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genetics
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physiology
9.Study on genotypes and geographical distribution of 58 strains of Yersinia pestis in Gansu.
Peng-fei GE ; Hong ZHANG ; Zhao-biao GUO ; Ke-jun MIAO ; Da-qin XU ; Wen-ping DA ; Bin WU ; Li-min GUO ; Ya-jun GE ; Guo-juan CHEN ; Tao-xia MU ; Jin-xiao XI
Chinese Journal of Epidemiology 2010;31(7):840-840
Animals
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China
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epidemiology
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Genotype
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Geography
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Humans
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Marmota
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microbiology
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Plague
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epidemiology
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microbiology
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Yersinia pestis
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classification
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genetics
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isolation & purification
10.Source tracing of the Yersinia pestis strains isolated from Heqing county, Yunnan province in 2017.
L Y SHI ; Y B DING ; H L TAN ; Y GUO ; H P ZHANG ; C J DUAN ; W LI ; P WANG
Chinese Journal of Epidemiology 2018;39(7):983-987
Objective: To understand the genotype of the Yersinia (Y.) pestis strains isolated from Heqing county, Yunnan province in 2017 and provide evidence for the prevention and control of plague in this area. Methods: Ten Y. pestis strains isolated from Heqing were typed by the detections of different region (DFR) and clustered regularly interspaced short palindromic repeats (CRISPRs) as well as multiple-locus variable-number tandem repeat analysis (MLVA). And the results were compared with those of the 93 Y. pestis strains from the adjacent plague foci of Heqing obtained from the established database for clustering analysis. Results: The results showed that Heqing strains had the same type of DFR (Genomovar 05) and CRISPRs (Cluster Ca7, Type 22) with isolates from the plague focus in Lijiang. Heqing strains and Lijiang strains were in the same cluster in MST and only VNTR loci N2117 and M23 of Heqing strains were different from that of Lijiang strains. Conclusion: The Y. pestis strains isolated from Heqing in 2017 were highly homogenous with the strains isolated from wild rodents in plague focus in Lijiang, and Heqing plague might be the result of further southward spread of Lijiang plague.
Animals
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China/epidemiology*
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Epidemiological Monitoring
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Genotype
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Minisatellite Repeats
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Molecular Typing
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Plague/microbiology*
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Rodentia/microbiology*
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Yersinia pestis/pathogenicity*