Evidence map›Paper›PMID 25928441›Full record

ArticleParasites & vectors2015

Transmission efficiency of the plague pathogen (Y. pestis) by the flea, Xenopsylla skrjabini, to mice and great gerbils.

Yujiang Zhang, Xiang Dai, Qiguo Wang, Hongjian Chen, Weiwei Meng, Kemei Wu, Tao Luo, Xinhui Wang, Azhati Rehemu, Rong Guo and 4 more

Open access · goldAbstract read
In one paragraph

Article in Parasites & vectors, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.0field-weighted citation impact, top 13% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
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  9. Phenotypic and Molecular Genetic Characteristics ofThe American journal of tropical medicine and hygiene · 2018
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors at 4 institutions in 2 countries.

Yujiang ZhangThe Center for Disease Control and Prevention of the Xinjiang Uygur Autonomous Region, Urumqi, 830002, China. xjsyzhang@163.com.
Xiang DaiThe Center for Disease Control and Prevention of the Xinjiang Uygur Autonomous Region, Urumqi, 830002, China. xjsydx@163.com.
Qiguo WangThe Center for Disease Control and Prevention of the Xinjiang Uygur Autonomous Region, Urumqi, 830002, China. wqg801021@126.com.
Hongjian ChenQinghai Institute for Endemic Diseases Prevention and Control, Xining, 811602, China. mjy70315@163.com.
Weiwei MengThe Center for Disease Control and Prevention of the Xinjiang Uygur Autonomous Region, Urumqi, 830002, China. mww_1980@126.com.
Kemei WuQinghai Institute for Endemic Diseases Prevention and Control, Xining, 811602, China. qhxnwkm@sina.com.
Tao LuoThe Center for Disease Control and Prevention of the Xinjiang Uygur Autonomous Region, Urumqi, 830002, China. lt7912@126.com.
Xinhui WangThe Center for Disease Control and Prevention of the Xinjiang Uygur Autonomous Region, Urumqi, 830002, China. wangxh6502@163.com.
Azhati RehemuThe Center for Disease Control and Prevention of the Xinjiang Uygur Autonomous Region, Urumqi, 830002, China. azt6710@163.com.
Rong GuoThe Center for Disease Control and Prevention of the Xinjiang Uygur Autonomous Region, Urumqi, 830002, China. feizaopaogr@sina.com.
Xiaotao YuQinghai Institute for Endemic Diseases Prevention and Control, Xining, 811602, China. yxt@qq.com.
Ruifu YangState Key Laboratory of Pathogen and Biosecurity, Beijing Institute of Microbiology and Epidemiology, Beijing, 100071, China. ruifuyang@gamil.com.
Hanli CaoThe Center for Disease Control and Prevention of the Xinjiang Uygur Autonomous Region, Urumqi, 830002, China. chl2621215@126.com.
Yajun SongState Key Laboratory of Pathogen and Biosecurity, Beijing Institute of Microbiology and Epidemiology, Beijing, 100071, China. songyajun88@gmail.com.
Centers for Disease Control and Prevention · USQinghai Institute for Endemic Diease Prevention and Control · CNInstitute of Microbiology · CNXinjiang Uygur Autonomous Region Disease Prevention and Control Center · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPlague, a zoonotic disease caused by Yersinia pestis, is characterized by its ability to persist in the plague natural foci. Junggar Basin plague focus was recently identified in China, with Rhombomys opimus (great gerbils) and Xenopsylla skrjabini as the main reservoir and vector for plague. No transmission efficiency data of X. skrjabini for Y. pestis is available till now.

methodsIn this study, we estimated the median infectious dose (ID50) and the blockage rates of X. skrjabini with Y. pestis, by using artificial feeders. We then evaluated the flea transmission ability of Y. pestis to the mice and great gerbils via artificial bloodmeal feeding. Finally, we investigated the transmission of Y. pestis to mice with fleas fed by infected great gerbils.

resultsID50 of Y. pestis to X. skrjabini was estimated as 2.04 × 10(5) CFU (95% CI, 1.45 × 10(5) - 3.18 × 10(5) CFU), around 40 times higher than that of X. cheopis. Although fleas fed by higher bacteremia bloodmeal had higher infection rates for Y. pestis, they lived significantly shorter than their counterparts. X. skrjabini could get fully blocked as early as day 3 post of infection (7.1%, 3/42 fleas), and the overall blockage rate of X. cheopis was estimated as 14.9% (82/550 fleas) during the 14 days of investigation. For the fleas infected by artificial feeders, they seemed to transmit plague more efficiently to great gerbils than mice. Our single flea transmission experiments also revealed that, the transmission capacity of naturally infected fleas (fed by infected great gerbils) was significantly higher than that of artificially infected ones (fed by artificial feeders).

conclusionOur results indicated that ID50 of Y. pestis to X. skrjabini was higher than other fleas like X. cheopis, and its transmission efficiency to mice might be lower than other flea vectors in the artificial feeding modes. We also found different transmission potentials in the artificially infected fleas and the naturally infected ones. Further studies are needed to figure out the role of X. skrjabini in the plague epidemiological cycles in Junggar Basin plague focus.

Indexed as

Disease Models, AnimalGerbillinaeMiceAnimalsChinaFemaleHumansInsect VectorsPlagueXenopsyllaYersinia pestisZoonoses

Identifiers

PMID25928441
PMCPMC4429828
OpenAlexW2114372919

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.