Evidence map›Paper›PMID 39383151›Full record

ArticlePLoS neglected tropical diseases2024

Usefulness of next-generation sequencing for laboratory diagnosis of rickettsiosis.

Fanfan Xing, Chaowen Deng, Jinyue Huang, Yanfei Yuan, Zhendong Luo, Simon K F Lo, Susanna K P Lau, Patrick C Y Woo

Abstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Human infection by an unclassifiedNew microbes and new infections · 2026
    Article
  2. Article
  3. Frontiers in pediatrics · 2026
    Article
  4. Article
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

8 authors.

Fanfan XingDepartment of Infectious Diseases and Microbiology, The University of Hong Kong - Shenzhen Hospital, Shenzhen, Guangdong, China.ORCID 0000-0001-8233-5127
Chaowen DengDepartment of Infectious Diseases and Microbiology, The University of Hong Kong - Shenzhen Hospital, Shenzhen, Guangdong, China.
Jinyue HuangDepartment of Infectious Diseases and Microbiology, The University of Hong Kong - Shenzhen Hospital, Shenzhen, Guangdong, China.
Yanfei YuanDepartment of Infectious Diseases and Microbiology, The University of Hong Kong - Shenzhen Hospital, Shenzhen, Guangdong, China.
Zhendong LuoDepartment of Medical Imaging, The University of Hong Kong - Shenzhen Hospital, Shenzhen, Guangdong, China.
Simon K F LoDepartment of Infectious Diseases and Microbiology, The University of Hong Kong - Shenzhen Hospital, Shenzhen, Guangdong, China.
Susanna K P LauDepartment of Microbiology, School of Clinical Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Pokfulam, Hong Kong, China.
Patrick C Y WooDepartment of Microbiology, School of Clinical Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Pokfulam, Hong Kong, China.ORCID 0000-0001-9401-1832

Funding

Higher Education Sprout Project by the Ministry of Education in Taiwan MOE-113-S-0023-ASanming Project of Medicine in Shenzhen, China SZSM201911014
6 · The paper itself

Abstract

Rickettsiosis includes a diversity of culture-negative non-specific systemic infections. Laboratory diagnosis of rickettsiosis is often not easy. In this 12-month study, six patients with a variety of rickettsia infections of the spotted fever group, typhus group and scrub typhus were diagnosed directly or indirectly by metagenomic next-generation sequencing (mNGS). The patient with Japanese spotted fever was rapidly made when mNGS analysis of the patient's blood revealed Rickettsia japonica sequences. For the two patients with Rickettsia felis chest infections, the bacterium was detected in the bronchoalveolar lavage of one case and lung biopsy of the other. Both patients had underlying malignancies, carcinoma of the breast and carcinoma of the lung respectively, and were on chemotherapy with immunosuppressive effect. For the remaining three patients who presented over a period of 13 weeks, all had fever, headache and the typical eschar. They also had increased serum transaminases and responded promptly to doxycycline. However, the Weil-Felix test results of all three patients were negative. Since we considered the three cases typical of rickettsiosis, we submitted their serum samples for mNGS analysis. Results showed that Orientia tsutsugamushi sequences were present in the serum of one case. In view of the positive mNGS results, we repeated the Weil-Felix test for the residual sera of all three patients and it revealed that those of the other two cases showed OX-19 titers of 1:640 and 1:160 respectively, inferring that these two patients probably had rickettsiosis of the typhus group. As for the patient positive for O. tsutsugamushi sequences, we also detected IgM for O. tsutsugamushi in the serum, which double confirmed that it was a case of scrub typhus. mNGS is an important molecular tool and can complement serology for laboratory diagnosis of rickettsiosis.

Indexed as

High-Throughput Nucleotide SequencingRickettsiaRickettsia InfectionsAdultAgedFemaleHumansMaleMetagenomicsMiddle AgedMolecular Diagnostic TechniquesOrientia tsutsugamushiScrub Typhus

Identifiers

PMID39383151
PMCPMC11463775

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Registered trials

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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.