Evidence map›Paper›PMID 42288861›Full record

ArticleParasites & vectors2026

First molecular evidence of Rickettsia spp. in Triatoma rubrofasciata: implications for vector ecology and zoonotic transmission.

Binglian Qin, Wenting Wei, Lili Tang, Peichao Deng, Xiaoquan Liu, Ling Li, Qingan Zhou, Yuanlin Hou, Huitong Pan, Jiaming Liang and 5 more

Abstract read
In one paragraph

Article in Parasites & vectors, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

15 authors.

Binglian Qin *Parasitology Department, School of Basic Medical Sciences, Guangxi Medical University, No.22 Shuangyong Road, Qingxiu District, Nanning, 530021, China.
Wenting Wei *Parasitology Department, School of Basic Medical Sciences, Guangxi Medical University, No.22 Shuangyong Road, Qingxiu District, Nanning, 530021, China.
Lili Tang *Parasitology Department, School of Basic Medical Sciences, Guangxi Medical University, No.22 Shuangyong Road, Qingxiu District, Nanning, 530021, China.
Peichao DengLianyungang Customs Integrated Technology Center, Lianyungang, People's Republic of China.
Xiaoquan LiuParasitology Department, School of Basic Medical Sciences, Guangxi Medical University, No.22 Shuangyong Road, Qingxiu District, Nanning, 530021, China.
Ling LiThe First People's Hospital of Nanning, Nanning, People's Republic of China.
Qingan ZhouAnimal Disease Prevention and Control Center of Guangxi Zhuang Autonomous Region, Nanning, People's Republic of China.
Yuanlin HouParasitology Department, School of Basic Medical Sciences, Guangxi Medical University, No.22 Shuangyong Road, Qingxiu District, Nanning, 530021, China.
Huitong PanParasitology Department, School of Basic Medical Sciences, Guangxi Medical University, No.22 Shuangyong Road, Qingxiu District, Nanning, 530021, China.
Jiaming LiangParasitology Department, School of Basic Medical Sciences, Guangxi Medical University, No.22 Shuangyong Road, Qingxiu District, Nanning, 530021, China.
Xiaoyin FuParasitology Department, School of Basic Medical Sciences, Guangxi Medical University, No.22 Shuangyong Road, Qingxiu District, Nanning, 530021, China.
Shanshan HeParasitology Department, School of Basic Medical Sciences, Guangxi Medical University, No.22 Shuangyong Road, Qingxiu District, Nanning, 530021, China.
Yanwen LiParasitology Department, School of Basic Medical Sciences, Guangxi Medical University, No.22 Shuangyong Road, Qingxiu District, Nanning, 530021, China. 2506345708@qq.com.
Dengyu LiuParasitology Department, School of Basic Medical Sciences, Guangxi Medical University, No.22 Shuangyong Road, Qingxiu District, Nanning, 530021, China. 33547533@qq.com.
Yunliang ShiParasitology Department, School of Basic Medical Sciences, Guangxi Medical University, No.22 Shuangyong Road, Qingxiu District, Nanning, 530021, China. syunliang2008@126.com.

Funding

National Natural Science Foundation of China No.82260413Youth Science Foundation of Guangxi Medical University GXMUYSF202201
6 · The paper itself

Abstract

backgroundRickettsia is an emerging global pathogen with incompletely understood transmission cycles. While triatomine bugs are established vectors for Trypanosoma cruzi, their potential role in the ecology of Rickettsia spp. remains unexplored. This study investigated the presence and genetic characteristics of Rickettsia spp. in Triatoma rubrofasciata and sympatric hosts in southern China.

methodsA total of 362 T. rubrofasciata specimens including the fecal samples, head tissues and gut were screened for Rickettsia DNA using nested PCR targeting six genes (groEL, rrs, gltA, 17-kDa, ompA, and ompB). In addition, 64 fleas, 136 ticks, and 69 wild rodents were tested. Positive amplicons were sequenced and subjected to phylogenetic analysis.

resultsRickettsia DNA was detected in eight (2.2%, 8/362) T. rubrofasciata specimens, with Rickettsia felis specifically identified in four of these positive samples; the species of the remaining four could not be determined. The bacterium was detected across multiple anatomical sites, including the head (which contains the salivary glands), the gut, and fecal samples. Surveillance of sympatric hosts revealed a markedly higher prevalence in fleas (57.8%) and wild rats (4.3%), whereas ticks harbored a distinct agent related to Candidatus Rickettsia jingxinensis (29.4%). Genomic analyses indicated high conservation of key loci among R. felis strains across hosts, with a stable ompA gene variation distinguishing vector- and rodent-derived lineages. Phylogenetically, all R. felis sequences formed a distinct clade separate from tick-associated rickettsiae.

conclusionsThis study confirms for the first time the presence of Rickettsia in T. rubrofasciata, including R. felis and Rickettsia sp. The R. felis was found co-circulating in fleas and rodents, while ticks harbored a distinct Rickettsia, indicating separate transmission cycles in sympatric hosts. Genetic divergence in ompA further suggests host-adaptive evolution between vector- and rodent-associated strains. These findings suggest that T. rubrofasciata may serve as a previously unrecognized interface in the epidemiology of flea-borne spotted fever in southern China. They also highlight the expanded vector range of Rickettsia and underscoring the ecological complexity of its transmission, calling for broader surveillance of nontraditional vectors in endemic regions.

Indexed as

Insect VectorsRickettsiaRickettsia InfectionsTriatomaZoonosesAnimalsChinaDNA, BacterialPhylogenyPolymerase Chain ReactionRodentiaSiphonapteraTicksDNA, BacterialMolecular characteristicsMolecular detectionOne HealthRickettsia felisSouthern ChinaTriatoma rubrofasciata

Identifiers

PMID42288861
PMCPMC13330430

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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.