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CASE REPORT article

Front. Pediatr., 01 September 2023
Sec. Pediatric Infectious Diseases

Pediatric pulmonary infection caused by oral obligate anaerobes: Case Series

\r\nLai ZhijunLai ZhijunYang WenhaiYang WenhaiZeng PeibinZeng PeibinLuo Qingming
\r\nLuo Qingming*
  • Department of Pediatric Intensive Care Unit, Dongguan Children's Hospital Affiliated to Guangdong Medical University, Dongguan, China

Background: Pneumonia is quite common in people with chronic bedridden, severe malnutrition and underlying diseases of cerebral palsy. Although poor oral hygiene and inadequate airway protection are risk factors, case reports of childhood pneumonia caused by oral obligate anaerobes are rare.

Introduction: We reported 4 cases of oral anaerobic pneumonia and empyema diagnosed by the pediatric intensive care unit (PICU) of our hospital.

Discussion: No bacteria were detected in sputum bacterial culture, pleural water bacterial culture and blood culture of the four children. Considering that multiple sputum cultures were negative, the pleural effusion and bronchoalveolar lavage fluid were subjected to next-generation sequencing (NGS) to identify the pathogen causing pneumonia. The results found oral obligate anaerobes represented by Parvimonas micra and Porphyromonas gingivalis. After identifying the pathogenic bacteria, we changed to piperacillin tazobactam combined with metronidazole for anti-infection treatment, and the pneumonia in the above patients was improved. In addition, all four patients had different basic medical histories, and long-term bed rest, severe malnutrition, poor oral hygiene and insufficient airway protection were all high risk factors for oral anaerobic pneumonia in these children.

Conclusion: Oral obligate anaerobes are one of the pathogens to consider for pneumonia in the elderly, but they may be easily overlooked in pediatric groups. Therefore, when receiving children with high-risk factors, we should be alert to the possibility of oral obligate anaerobic bacteria infection. Educating family members to pay attention to children's oral hygiene plays an important role in preventing oral obligatory anaerobic bacteria pneumonia. NGS can be used as a rapid diagnostic method when sputum culture cannot distinguish between pathogens.

1. Background

Oral obligate anaerobes are important pathogens of pneumonia in the elderly, but case reports of obligate anaerobes-associated pneumonia in children are rare. Oral obligate anaerobes include Parvimonas micra and Porphyromonas gingivalis, which can be detected in oral dental plaque (1, 2). There have been case reports of Parvimonas micra or Porphyromonas gingivalis causing (3), phlebitis (4), abdominal abscess (5) and intracranial abscess (6). As one of the common pathogenic bacteria of aspiration pneumonia in the elderly population (7, 8), anaerobic lung infection is associated with oral secretion aspiration, poor oral hygiene conditions and inadequate airway protection (9).

Anaerobic pneumonia is relatively rare in normal children, but some special children have high risk factors for anaerobic pneumonia. Clinical antimicrobial treatment of community-acquired pneumonia in children caused by bacteria does not cover anaerobic bacteria, so uncommon pathogens often need to be considered in the case of poor conventional anti-infective treatment. Because oral obligate anaerobes are difficult to define by bacterial culture, early adoption of NGS can facilitate rapid diagnosis to initiate appropriate anti-infective treatment.

2. Methods of NGS

2.1. Sample processing and DNA extraction

1.5–3 ml BALF sample from patient was collected according to standard procedures. 1.5 ml microcentrifuge tube with 0.6 ml sample and 250 µl 0.5 mm glass bead were attached to a horizontal platform on a vortex mixer and agitated vigorously at 2800–3200 rpm for 30 min. Then 7.2 µl lysozyme was added for wall-breaking reaction. 0.3 ml sample was separated into a new 1.5 ml microcentrifuge tube and DNA was extracted using the TIANamp Micro DNA Kit (DP316, TIANGEN BIOTECH) according to the manufacturer's recommendation. The extracted DNA specimens were used for the construction of DNA libraries (10).

2.2. RNA library construction and sequencing

Microbial RNA was extracted from BALF samples using a QIAamp Viral RNA Mini Kit (Qiagen, 250, Germany) according to the manufacturer's recommendations. RNA was fragmented, reverse-transcribed, end-repaired, ligated to adapters, and amplified by PCR.

2.3. Construction of DNA libraries and sequencing

Then, DNA libraries were constructed through DNA-fragmentation, end-repair, adapter-ligation and PCR amplification. Agilent 2,100 was used for quality control of the DNA libraries. Quality qualified libraries were pooled, DNA Nanoball (DNB) was made and sequenced by BGISEQ-50 /MGISEQ-2000 platform (11).

2.4. Bioinformatic analysis

High-quality sequencing data were generated by removing low-quality reads, followed by computational substraction of human host sequences mapped to the human reference genome (hg19) using Burrows–Wheeler Alignment (12). The remaining data by removal of low-complexity reads were classified by simultaneously aligning to Pathogens metagenomics Database (PMDB), consisting of bacteria, fungi, viruses and parasites. The classification reference databases were downloaded from NCBI (ftp://ftp.ncbi.nlm.nih.gov/genomes/). RefSeq contains 4,945 whole genome sequence of viral taxa, 6,350 bacteral genomes or scaffolds, 1,064 fungi related to human infection, and 234 parasites associated with human diseases.

3. Case introduction

From 2020 to 2022, four children with pneumonia diagnosed as oral obligate anaerobic bacteria were admitted to the PICU of our hospital.

Three of the four children were male and 1 female. Their mean age was 10.3 years (age range from 8 to 13 years). All patients had different underlying diseases (Down syndrome (n = 1), cerebral palsy (n = 2), hypophrenia (n = 1), severe malnutrition (n = 4), nasal tube feeding (n = 3)) (Table 1). All four children had poor oral hygiene, more tartar, and different degrees of dental caries.

TABLE 1
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Table 1. Age, gender, underlying disease, nutritional status, feeding practices, and prognosis.

Clinical symptoms included fever (n = 4), cough (n = 4), shortness of breath (n = 2), haemoptysis (n = 1), and respiratory failure (n = 1). Only one child required mechanical ventilation during hospitalization, and three others required only low-flow oxygen support. Finally, the four children were improved and discharged (Table 2). All patients had computed tomography scans showing pleural effusion (n = 4) and lung abscess (n = 4) (Figure 1). One of the children underwent lung necrosis tissue resection, and massive leukocyte infiltration was seen in the removed lung histopathological sections (Figure 2).

TABLE 2
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Table 2. Clinical symptoms and respiratory support status.

FIGURE 1
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Figure 1. Pulmonary CT findings: (A,B) are the CT of case 1. (C,D) are the CT of case 2. (E,F) are the CT of case 3. (G,H) are CT of case 4.

FIGURE 2
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Figure 2. Plot of the lung damaged tissue and pathological sections in case 4. Extensive leukocyte infiltration was seen in the pathological sections.

In terms of etiology detection, all the children with sputum bacterial culture and blood culture did not detect bacteria. Three children underwent thoracentesis during hospitalization and sent pleural effusion samples for NGS to identify the pathogen. Another child underwent fiberoptic bronchoscopic alveolar lavage and sent this child's alveolar lavage fluid for NGS. NGS tests in 4 children showed that Porphyromonas (n = 4), Parvimonas micra (n = 3), Fusobacterium (n = 2), Streptococcus (n = 2), Pyramidobacter piscolens (n = 1), Peptostreptococcus stomatis (n = 1), Filifactor alocis (n = 1), Prevotella oris (n = 1), Tannerella forsythia (n = 1), Bacteroides heparinolyticus (n = 1), Solobacterium moorei (n = 1), Dialister pneumosintes (n = 1), and Catonella morbi (n = 1) (Table 3).

TABLE 3
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Table 3. The reads of pathological detection in NGS report.

4. Discussion

Poor oral hygiene has been shown to be associated with obligate anaerobic bacteria in the lower respiratory tract by Ryosuke Hata et al. (9). The plaque biofilm on the tooth surface is a large reservoir of bacteria and in specific circumstances these bacteria may cause lower respiratory tract infection (13). These oral colonizing bacteria are also important pathogens causing aspiration pneumonia (14). Although Ryosuke Hata et al. targeted the elderly group and did not conduct a studies of children, our reported cases were similar to the elderly group in the above study. They also lack the ability to maintain good oral hygiene independently, and they also have airway protection or swallowing disorders. All of the above reasons are the high risk factors of oral obligatory anaerobic bacteria pneumonia in this group.

In our reported cases, the pathogens with the highest percentage of detection were Porphyromonas gingivalis as well as Parvimonas micra. Both are obligate anaerobes with oral colonization, and they both need to reproduce in a strictly sterile environment. In general, obligate anaerobic bacteria can hardly survive in an oxygenated environment in the lungs. But because the host has long-term bed or the cough reflex drops in the lungs, it may create a local hypoxia environment, creating conditions for the growth of obligate anaerobic bacteria to thrive. Before all patients underwent CT, we communicated with the parents about the condition, and none of the parent did consent for chest enhanced CT, and therefore the results of chest enhanced CT were lacking. The CT examinations of all four children were suggestive of varying degrees of pleural effusion. We all know that the pleural cavity is originally a confined space, which is conducive to the growth of obligate anaerobic bacteria. We kept samples of diseased lung tissue, but limited by the high cost of NGS examination, we failed to conduct NGS examination of diseased tissue (Figure 2). Pleural infection caused by an anaerobe is the cause of a large pleural effusion. The pleural effusion extracted in case 4 in our report is brownish (Figure 3).

FIGURE 3
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Figure 3. The pleural effussion of case 4. The patient's pleural effusion was brownish.

In our report, there were two cases each of left and right pleural effusion. Although it is generally believed that aspiration pneumonia is more likely in the right lung, not all cases developed infection in the right lung. We considered that this may be associated with maintaining different positions in different patients. A prolonged left lateral position may be more likely to cause aspiration pneumonia in the left lung.

All sputum and blood cultures during hospitalization of the children in this case report were negative. Bacterial cultures of pleural effusion were performed in three children, but these bacterial cultures were negative. This is related to the specific growth conditions of obligate anaerobes, so it is often difficult to diagnose anaerobic infections clinically by bacterial culture. We found that NGS has been applied in the diagnosis of encephalitis (15) and infectious pancreatitis (16). Therefore, when the initial stage of anti-infection treatment effect is not satisfactory, We performed NGS examinations to clarify the etiology. When we have obtained the NGS report, we thought there were 2 main reasons support our consideration of anaerobe-associated pneumonia: ① These patients were treated with piperacillin sulbactam/piperacillin tazobactam, but the effect of treatment was unsatisfy. This suggests that the infectious source is not within the coverage of this antibiotic. ② In the NGS report, the relevant pathogen was clearly detected. As we knew, piperacillin sulbactam/piperacillin tazobactam is unsatisfy in treating infections caused by these pathogens.

We immediately switched to metronidazole (7.5 mg/kg q8h) combined with piperacillin tazobactam (4:1,50 mg/kg q8h) after confirming the NGS results. After adjusting the anti-infection treatment regimen, all the children improved and were eventually discharged. NGS as a novel detection method helps detecting special pathogens. Despite the high price of NGS, it is still a clinically important test.

5. Conclusion

The elderly and the immunocompromised group were previously considered to be at high risk for anaerobic pneumonia (17, 18), but some special child groups may be easily overlooked (19). Such children often have high-risk factors such as poor oral hygiene, inadequate airway protection, swallowing dysfunction, long-term bed and malnutrition. In treating such children, we need to consider special etiological infections possible if conventional anti-infective treatment is ineffective. NGS may be an effective means for early and rapid diagnosis. After identifying the cause, the targeted anti-infection regimen is critical to the prognosis of the child.

For families with such special children, health care workers need adequate health education to develop good awareness of the disease. Grasping the ability of effective oral care and cleaning has an irreplaceable role in reducing the occurrence of anaerobic bacteria pneumonia.

Data availability statement

The original contributions presented in the study are included in the article/supplementary material, further inquiries can be directed to the corresponding author/s.

Ethics statement

The studies involving humans were approved by the Ethical Review Committee of Dongguan Children's Hospital. The studies were conducted in accordance with the local legislation and institutional requirements. The human samples used in this study were acquired from primarily isolated as part of your previous study for which ethical approval was obtained. Written informed consent for participation was not required from the participants or the participants’ legal guardians/next of kin in accordance with the national legislation and institutional requirements. Written informed consent was obtained from the individual(s), and minor(s)' legal guardian/next of kin, for the publication of any potentially identifiable images or data included in this article.

Author contributions

YW, LZ, and ZP all participated in the diagnosis and treatment process of the above patients and collected relevant clinical data. YW and LZ wrote the first draft of the report. LQ reviewed and revised the first draft. All authors contributed to the article and approved the submitted version.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher's note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

References

1. Shimizu K, Horinishi Y, Sano C, Ohta R. Infection route of parvimonas micra: a case report and systematic review. Healthcare (Basel). (2022) 10(9):1727. doi: 10.3390/healthcare10091727

PubMed Abstract | CrossRef Full Text | Google Scholar

2. Meng F, Li R, Ma L, Liu L, Lai X, Yang D, et al. Porphyromonas gingivalis promotes the motility of esophageal squamous cell carcinoma by activating NF-κB signaling pathway. Microbes Infect. (2019) 21(7):296–304. doi: 10.1016/j.micinf.2019.01.005

PubMed Abstract | CrossRef Full Text | Google Scholar

3. Norimatsu Y, Ohno Y. First report of subcutaneous abscess caused by porphyromonas gingivalis. IDCases. (2020) 21:e00917. doi: 10.1016/j.idcr.2020.e00917

PubMed Abstract | CrossRef Full Text | Google Scholar

4. Shinha T, Caine V. Pylephlebitis due to parvimonas micra. Infect Dis Clin Pract. (2015) 24(1):54–6. doi: 10.1097/IPC.0000000000000286

CrossRef Full Text | Google Scholar

5. Ang MY, Dymock D, Tan JL, Thong MH, Tan QK, Wong GJ, et al. Genome sequence of parvimonas micra strain A293, isolated from an abdominal abscess from a patient in the United Kingdom. Genome Announc. (2013) 1(6):e01025–13. doi: 10.1128/genomeA.01025-13

PubMed Abstract | CrossRef Full Text | Google Scholar

6. Kichenbrand C, Marchal A, Mouraret A, Hasnaoui N, Guillet J, Rech F, et al. Brain abscesses and intracranial empyema due to dental pathogens: case series. Int J Surg Case Rep. (2020) 69:35–8. doi: 10.1016/j.ijscr.2020.03.025

PubMed Abstract | CrossRef Full Text | Google Scholar

7. Awano S, Ansai T, Takata Y, Soh I, Akifusa S, Hamasaki T, et al. Oral health and mortality risk from pneumonia in the elderly. J Dent Res. (2008) 87(4):334–9. doi: 10.1177/154405910808700418

PubMed Abstract | CrossRef Full Text | Google Scholar

8. Muthu J, Muthanandam S, Mahendra J. Mouth the mirror of lungs: where does the connection lie? Front Med. (2016) 10(4):405–9. doi: 10.1007/s11684-016-0476-5

PubMed Abstract | CrossRef Full Text | Google Scholar

9. Hata R, Noguchi S, Kawanami T, Yamasaki K, Akata K, Ikegami H, et al. Poor oral hygiene is associated with the detection of obligate anaerobes in pneumonia. J Periodontol. (2020) 91(1):65–73. doi: 10.1002/JPER.19-0043

PubMed Abstract | CrossRef Full Text | Google Scholar

10. Long Y, Zhang Y, Gong Y, Sun R, Su L, Lin X, et al. Diagnosis of sepsis with cell-free DNA by next-generation sequencing technology in ICU patients. Arch Med Res. (2016) 47(5):365–71. doi: 10.1016/j.arcmed.2016.08.004

PubMed Abstract | CrossRef Full Text | Google Scholar

11. Jeon YJ, Zhou Y, Li Y, Guo Q, Chen J, Quan S, et al. The feasibility study of non-invasive fetal trisomy 18 and 21 detection with semiconductor sequencing platform. PLoS One. (2014) 9(10):e110240. doi: 10.1371/journal.pone.0110240

PubMed Abstract | CrossRef Full Text | Google Scholar

12. Li H, Durbin R. Fast and accurate short read alignment with Burrows–Wheeler transform. Bioinformatics. (2009) 25(14):1754–60. doi: 10.1093/bioinformatics/btp324

PubMed Abstract | CrossRef Full Text | Google Scholar

13. Okuda K, Kimizuka R, Abe S, Kato T, Ishihara K. Involvement of periodontopathic anaerobes in aspiration pneumonia. J Periodontol. (2005) 76(11 Suppl):2154–60. doi: 10.1902/jop.2005.76.11-S.2154

CrossRef Full Text | Google Scholar

14. Heo SM, Sung RS, Scannapieco FA, Haase EM. Genetic relationships between candida albicans strains isolated from dental plaque, trachea, and bronchoalveolar lavage fluid from mechanically ventilated intensive care unit patients. J Oral Microbiol. (2011) 3:6362. doi: 10.3402/jom.v3i0.6362

CrossRef Full Text | Google Scholar

15. Stebner A, Ensser A, Geißdörfer W, Bozhkov Y, Lang R. Molecular diagnosis of polymicrobial brain abscesses with 16S-rDNA-based next-generation sequencing. Clin Microbiol Infect. (2021) 27(1):76–82. doi: 10.1016/j.cmi.2020.03.028

PubMed Abstract | CrossRef Full Text | Google Scholar

16. Sun N, Chen Y, Zhang J, Cao J, Huang H, Wang J, et al. Identification and characterization of pancreatic infections in severe and critical acute pancreatitis patients using 16S rRNA gene next generation sequencing. Front Microbiol. (2023) 14:1185216. doi: 10.3389/fmicb.2023.1185216

PubMed Abstract | CrossRef Full Text | Google Scholar

17. Cobo F, Borrego J, Rojo MD, Navarro-Marí JM. Polymicrobial anaerobic bacteremia due to Atopobium rimae and Parvimonas micra in a patient with cancer. Anaerobe. (2018) 54:260–3. doi: 10.1016/j.anaerobe.2018.02.002

PubMed Abstract | CrossRef Full Text | Google Scholar

18. Nair GB, Niederman MS. Updates on community acquired pneumonia management in the ICU. Pharmacol Ther. (2021) 217:107663. doi: 10.1016/j.pharmthera.2020.107663

PubMed Abstract | CrossRef Full Text | Google Scholar

19. Rueda ZV, Aguilar Y, Maya MA, López L, Restrepo A, Garcés C, et al. Etiology and the challenge of diagnostic testing of community-acquired pneumonia in children and adolescents. BMC Pediatr. (2022) 22(1):169. doi: 10.1186/s12887-022-03235-z

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: obligate anaerobes, lung infection, children, next-generation sequencing, oral hygiene

Citation: Zhijun L, Wenhai Y, Peibin Z and Qingming L (2023) Pediatric pulmonary infection caused by oral obligate anaerobes: Case Series. Front. Pediatr. 11:1226706. doi: 10.3389/fped.2023.1226706

Received: 22 May 2023; Accepted: 18 August 2023;
Published: 1 September 2023.

Edited by:

George Grant, University of Aberdeen, United Kingdom

Reviewed by:

Takuichi Sato, Niigata University, Japan
Domingo Fernández Vecilla, Basurto University Hospital, Osakidetza Basque Health Service, Spain
Takayuki Hoshina, University of Occupational and Environmental Health Japan, Japan

© 2023 Zhijun, Wenhai, Peibin and Qingming. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Luo Qingming MTgwMTE1NjM2QHFxLmNvbQ==

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.