Skip to main content

Leptotrichia trevisanii bacteremia in a woman with systemic lupus erythematosus receiving high-dose chemotherapy

Abstract

Background

Leptotrichia species are aerotolerant, Gram-negative fusiform bacteria. Cases of bacteremia caused by Leptotrichia trevisanii in immunocompromised patients have been rarely reported.

Case presentation

A 33-year-old female with systemic lupus erythematosus (SLE) was admitted to the department of rheumatology with bleeding from a mucosal ulcer. One month previously, she had visited our hospital and begun to receive methotrexate therapy, but mis-dosed for nearly 1 month at home. Methotrexate toxicity resulted in a severe oral ulcer and bone marrow suppression. On day-7 of hospital admission, she developed a fever, and Gram-negative rods (Leptotrichia trevisanii) were detected in blood cultures. She was diagnosed with methotrexate poisoning followed by L. trevisanii bacteremia. After antibiotic and detoxification therapy, she recovered from bacteremia, and the oral ulcer and bone-marrow suppression improved obviously.

Conclusions

This is the first reported case of Leptotrichia trevisanii bacteremia in a SLE patient who took mis-dosed an immunosuppressant and had an oral mucosal lesion.

Peer Review reports

Background

Leptotrichia species are aerotolerant, Gram-negative fusiform bacteria that can inhabit the oral cavity, intestinal tract and genitalia [1]. Leptotrichia species have been implicated in periodontal disease, endocarditis, chorioamnionitis and arthritis, especially in immunocompromised patients [2,3,4]. Leptotrichia trevisanii bacteremia has been reported in patients with acute myeloid leukemia [5, 6], myelodysplastic syndrome [7] and febrile neutropenia [8]. Here, we describe a case of bacteremia due to L. trevisanii in a female with systemic lupus erythematosus (SLE) and methotrexate poisoning.

Case presentation

A 33-year-old female was diagnosed with SLE 3 years previously in another hospital. She visited our hospital in May 2018 due to pain in lower back and began to take methotrexate. Advice from her physician was methotrexate (10 mg) once a week, but she made the mistake of taking this dose every day. She developed severe bleeding from an ulcer in the oral mucosa, and was admitted to our hospital 1 month later. She was diagnosed with SLE and methotrexate poisoning.

Even though she had stopped using methotrexate, her white blood cell (WBC) count was 1.67 × 109/L, red blood cell (RBC) count was 3.02 × 109/L, hemoglobin level was 119 g/L, and platelet count was 66 × 109/L, which suggested bone suppression. On day-7 of hospital administration, the patient developed fever (38.3 °C) and infection was suspected. Laboratory analyses revealed a level of C-reactive protein (CRP) of 19.19 mg/L, lactate dehydrogenase (LDH) of 5 U/L, aspartate transaminase (AST) of 8 U/L, alanine transaminase (ALT) of 91 U/L, and erythrocyte sedimentation rate (ESR) of 23 mm/h. Blood samples were taken and empirical therapy with metronidazole and cefoperazone/tazobactam was started because of fever with oral mucositis. At day- 11 of hospital admission, spindle-shaped Gram-negative rods were isolated from one of four blood samples (Fig. 1). After 24 h of incubation in an anaerobic environment with 5% CO2, growth on blood agar showed light yellow-pigmented colonies that were smooth, gray, catalase-positive and oxidase-negative (Fig. 2). The organism was identified as Leptotrichia trevisanii by matrix-assisted laser desorption ionization- time of flight-mass spectrometry (MALDI-TOF-MS) undertaken on a Biotyper system (Bruker, Bremen, Germany) (Fig. 3). In addition, the organism was confirmed as L. trevisanii using 16S ribosomal RNA (rRNA) gene sequencing as described previously [9], which matched 98% with the L. trevisanii strain (NR 029805.1). Therefore, the patient was diagnosed with L. trevisanii bacteremia and received the therapy mentioned above continuously.

Fig. 1
figure 1

Gram stain preparation of the isolate colony in anaerobic condition (grown on a blood agar plate). Gram stain × 1,000

Fig. 2
figure 2

The form of colonies on a blood agar plate

Fig. 3
figure 3

Identification of L. trevisanii by MALDI-TOF MS a The spectrum of L. trevisanii. b, c Identification result of L. trevisanii

Next, we collected samples of the ulcer in the oral mucosa using a swab for anaerobic culture but L. trevisanii was not isolated, which might have been caused by exposure to an aerobic environment. After 10 days of treatment, the fever disappeared and the mucositis improved obviously. Routine blood analyses revealed the WBC count to be 11.19 × 109/L, RBC count to be 3.7 × 1012/L, hemoglobin level to be 110 g/L and platelet count to be 256 × 109/L, suggesting that bone-marrow suppression was also restored. Therefore, sepsis had resolved and there was no recurrence of bacteremia.

Discussion

Leptotrichia is one of six genera in the family Fusobacteriaceae in the phylum Fusobacteria [1]. The genus Leptotrichia contains a wide variety of species,such as L. buccalis, L. trevisanii, L. amnionii, L. goodfellowi, L. hofstadii, L. shahii, L. wadei, and L. hongkongensis [1, 10]. Leptotrichia species are anaerobic Gram-negative rods that inhabit the oral cavity, gastrointestinal tract, urogenital system and female genital tract of humans [11, 12].

Previous studies have shown that Leptotrichia species can be isolated as pathogens in endocarditis, periodontitis, chorioamnionitis, abscesses as well as wound infections after dog bites [4, 11]. Bacteremia caused by Leptotrichia species are rarely isolated from immunocompromised patients (e.g, those suffering from hematologic malignancies, cancer or acquired immune deficiency syndrome) [5, 11, 13, 14]. Leptotrichia species are not prevelant, but infection can be severe in immunosuppressed patients. Identification of Leptotrichia species can be difficult, and is likely to remain an underappreciated cause of anaerobic bloodstream infection due to the inherent difficulties associated with conventional laboratory assays [15]. Moreover, the clinical signs of infection with Leptotricha species are not specific because fever can occur in other Gram-negative bacterial infections. Therefore, misdiagnoses of infections due to Leptotrichia species with infections by Fusobacterium species, Capnocytophaga species or Lactobacillus species or the problems due to culture can obscure the clinical importance of Leptotrichia species. However, MALDI-TOF-MS and 16S rRNA gene sequencing can be employed to identify Leptotrichia species. Both of these methods are reliable and feasible for identification of some anaerobic species in microbiology laboratories that are difficult to identify using traditional phenotypic systems [6, 16]. Therefore, routine use of these new methods allows recongnition of more Leptotrichia isolates, which could also provide evidence for effective and timely therapy for patients.

L. trevisanii was described first by Tee et al. in 2001 [6]. L. trevisanii grow best in anaerobic environments, but they can grow readily aerobically with 5% CO2 on blood agar, and are recongized as the most aerotolerant species of this genus [1, 11]. On blood agar, colonies appear smooth, gray, with dark central spots, measuring ~ 2 mm. Gram stain reveals unsporulated, elongated, fusiform Gram-negative bacilli. L. trevisanii has been reported in bacteremia secondary to mucositis, periodontitis, abscesses, and catheter-related bloodstream infections as well as in patients: with hematologic malignancies; who have undergone bone transplantation; with solid tumors undergoing chemotherapy; with febrile neutropenia [5,6,7,8, 16,17,18]. Particullarly, patients who have undergone and hematopoietic stem-cell transplantation and who received high-dose chemotherapy, Leptotrichia species have been identified as major pathogens of bacteremia [12]. Chorioamnionitis and pelvic inflammatory diseases have also been reported to be caused by L. trevisanii [19, 20]. Therefore, Leptotrichia species as emerging pathogens can cause Leptotrichia anaerobic bloodstream infection in immunocompromised patients.

This is the first case of L. trevisanii bacteremia in a SLE patient diagnosed with methotrexate poisoning because of mis-dosing. Subsequently, she developed severe oral mucositis accompanied by neutropenia. Methotrexate poisoning is very rare, so we recommended that she take immunosuppressants according to the advice of her physician. Furthermore, not only patients with hematologic malignancies but also people with autoimmune diseases who take immunosuppressants (with the attendant loss of a normal mucosal barrier in oral or lower gastrointestinal tracts) should be considered as high-risk populations for Leptotrichia infection. Therefore, immunosuppression with severe mucositis and neutropenia are the primary risk factors for L. trevisanii bacteremia.

Conclusion

In conclusion, this is the first case of L. trevisanii bacteremia in a SLE patient with methotrexate poisoning. This species can be identified by MALDI-TOF- MS rapidly, reliably, and cost-effectively, which enables early appropriate antibiotic treatment and prevention of complications. Opportunistic pathogens and oral anaerobes, including L. trevisanii, should be screened completely, not limited to conventional agents, in immunocompromised patients who have oral mucositis.

Abbreviations

ALT:

Alanine aminotransferase

AST:

Aspartate transaminase

CRP:

C reaction protein

ESR:

Erythrocyte sedimentation rate

LDH:

Lactate dehydrogenase

MALDI-TOF MS:

Matrix-assisted laser desorption ionization time of flight spectrometry

RBC:

Red blood cell

rRNA:

Ribosomal RNA

SLE:

Systemic lupus erythematosus

WBC:

White blood cell

References

  1. Eribe ER, Paster BJ, Caugant DA, Dewhirst FE, Stromberg VK, Lacy GH, Olsen I. Genetic diversity of Leptotrichia and description of Leptotrichia goodfellowii sp. nov., Leptotrichia hofstadii sp. nov., Leptotrichia shahii sp. nov. and Leptotrichia wadei sp. nov. Int J syst Evol Microbiol. 2004;54(Pt 2):583–92.

    Article  CAS  Google Scholar 

  2. Goto M, Hitomi S, Ishii T. Bacterial arthritis caused by Leptotrichia amnionii. J Clin Microbiol. 2007;45(6):2082–3.

    Article  Google Scholar 

  3. Thilesen CM, Nicolaidis M, Lokebo JE, Falsen E, Jorde AT, Muller F. Leptotrichia amnionii, an emerging pathogen of the female urogenital tract. J Clin Microbiol. 2007;45(7):2344–7.

    Article  Google Scholar 

  4. Eribe ERK, Olsen I. Leptotrichia species in human infections II. J Oral Microbiol. 2017;9(1):1368848.

    Article  Google Scholar 

  5. Kumagai J, Takiguchi Y, Shono K, Suruga Y, Akiba Y, Yamamoto K, Terano T. Acute myelogenous leukemia with Leptotrichia trevisanii bacteremia. Intern Med. 2013;52(22):2573–6.

    Article  Google Scholar 

  6. Tee W, Midolo P, Janssen PH, Kerr T, Dyall-Smith ML. Bacteremia due to Leptotrichia trevisanii sp. nov. Eur J Clin Microbiol Infect Dis. 2001;20(11):765–9.

    Article  CAS  Google Scholar 

  7. Cooreman S, Schuermans C, Van Schaeren J, Olive N, Wauters G, Verhaegen J, Jeurissen A. Bacteraemia caused by Leptotrichia trevisanii in a neutropenic patient. Anaerobe. 2011;17(1):1–3.

    Article  CAS  Google Scholar 

  8. Higurashi Y, Tatsuno K, Fujimoto F, Kobayashi I, Ida K, Seto Y, Ohkusu K, Ezaki T, Okugawa S, Moriya K. Two cases of bacteremia caused by Leptotrichia trevisanii in patients with febrile neutropenia. J Infect Chemother. 2013;19(6):1181–4.

    Article  Google Scholar 

  9. Simmon KE, Croft AC, Petti CA. Application of SmartGene IDNS software to partial 16S rRNA gene sequences for a diverse group of bacteria in a clinical laboratory. J Clin Microbiol. 2006;44(12):4400–6.

    Article  CAS  Google Scholar 

  10. Woo PC, Wong SS, Teng JL, Leung KW, Ngan AH, Zhao DQ, Tse H, Lau SK, Yuen KY. Leptotrichia hongkongensis sp. nov., a novel Leptotrichia species with the oral cavity as its natural reservoir. J Zhejiang Univ Sci B. 2010;11(6):391–401.

    Article  Google Scholar 

  11. Eribe ER, Olsen I. Leptotrichia species in human infections. Anaerobe. 2008;14(3):131–7.

    Article  Google Scholar 

  12. Couturier MR, Slechta ES, Goulston C, Fisher MA, Hanson KE. Leptotrichia bacteremia in patients receiving high-dose chemotherapy. J Clin Microbiol. 2012;50(4):1228–32.

    Article  Google Scholar 

  13. Shah HN, Olsen I, Bernard K, Finegold SM, Gharbia S, Gupta RS. Approaches to the study of the systematics of anaerobic, gram-negative, non-sporeforming rods: current status and perspectives. Anaerobe. 2009;15(5):179–94.

    Article  CAS  Google Scholar 

  14. Kohler JL, Raoult D, Gallais H, Pons M, Peloux Y, Casanova P. Septicemia due to Leptotrichia buccalis in an immuno-suppressed patient. Sem Hop. 1982;58(30–31):1767–8.

    CAS  PubMed  Google Scholar 

  15. Patel JB, Clarridge J, Schuster MS, Waddington M, Osborne J, Nachamkin I. Bacteremia caused by a novel isolate resembling leptotrichia species in a neutropenic patient. J Clin Microbiol. 1999;37(6):2064–7.

    CAS  PubMed  PubMed Central  Google Scholar 

  16. Martín-Gutiérrez G, Parody R, Rodríguez N, Torres MJ, Lepe JA, Aznar J. Rapid identification of a Leptotrichia trevisanii catheter-related bloodstream infection using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry. JMM Case Rep. 2015;2(4):1–4. https://0-doi-org.brum.beds.ac.uk/10.1099/jmmcr.0.000036.

  17. Schrimsher JM, McGuirk JP, Hinthorn DR. Leptotrichia trevisanii sepsis after bone marrow transplantation. Emerg Infect Dis. 2013;19(10):1690–1.

    Article  Google Scholar 

  18. Sabater Cabrera C, Fernandez Blazquez A, Garcia Carus E. Bacteremia due to Leptotrichia trevisanii after an allogeneic bone marrow transplant. Enferm Infecc Microbiol Clin. 2017;35(6):389–90.

    Article  Google Scholar 

  19. Fontanals D, Garcia-Miralles C, Ballester R, Cochs B, Orellana R, Capilla S. Chorioamnionitis due to Leptotrichia trevisanii. Anaerobe. 2018;49:18–20.

    Article  Google Scholar 

  20. Mora-Palma JC, Rodriguez-Oliver AJ, Navarro-Mari JM, Gutierrez-Fernandez J. Emergent genital infection by Leptotrichia trevisanii. Infection. 2018. https://0-doi-org.brum.beds.ac.uk/10.1007/s15010-018-1175-8.

Download references

Acknowledgements

We thank Rui Xing for his help of providing the patient’s previous condition.

Funding

This work was supported by research grants from the National Mega Project on Major Infectious Disease Prevention (2017ZX10103005–007). The sequencing analysis of the strain was funded by the project.

Availability of data and materials

Not applicable.

Author information

Authors and Affiliations

Authors

Contributions

HYH wrote the manuscript. ZJC did the MALDI-TOF MS and 16S rRNA gene sequencing. LT and ZYS helped revise the manuscript. All authors have read and approved the final manuscript.

Corresponding author

Correspondence to Ziyong Sun.

Ethics declarations

Ethics approval and consent to participate

The study was approved by the ethical committee of Tongji hospital, Tongji Medical College, Huazhong University of Science and Technology. Informed written consent was obtained from the patient.

Consent for publication

Written informed consent for publication of the clinical details was obtained from the patient.

Competing interests

The authors declare that they have no competing interest.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Hou, H., Chen, Z., Tian, L. et al. Leptotrichia trevisanii bacteremia in a woman with systemic lupus erythematosus receiving high-dose chemotherapy. BMC Infect Dis 18, 661 (2018). https://0-doi-org.brum.beds.ac.uk/10.1186/s12879-018-3495-9

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://0-doi-org.brum.beds.ac.uk/10.1186/s12879-018-3495-9

Keywords