Skip to main content
Top
Published in: Infection 4/2020

Open Access 01-08-2020 | Computed Tomography | Original Paper

Metagenomic next-generation sequencing in the diagnosis of severe pneumonias caused by Chlamydia psittaci

Authors: Xiancheng Chen, Ke Cao, Yu Wei, Yajun Qian, Jing Liang, Danjiang Dong, Jian Tang, Zhanghua Zhu, Qin Gu, Wenkui Yu

Published in: Infection | Issue 4/2020

Login to get access

Abstract

Purpose

Chlamydia psittaci infection in humans can lead to serious clinical manifestations, including severe pneumonia, adult respiratory distress syndrome, and, rarely, death. Implementation of metagenomic next-generation sequencing (mNGS) gives a promising new tool for diagnosis. The clinical spectrum of severe psittacosis pneumonia is described to provide physicians with a better understanding and to highlight the rarity and severity of severe psittacosis pneumonia.

Methods

Nine cases of severe psittacosis pneumonia were diagnosed using mNGS. Retrospective analysis of the data on disease progression, new diagnosis tool, treatments, and outcomes, and the findings were summarised.

Results

Frequent symptoms included chills and remittent fever (100%), cough and hypodynamia (100%), and headache and myalgia (77.8%). All patients were severe psittacosis pneumonia developed respiratory failure, accompanied by sepsis in 6/9 patients. mNGS takes 48–72 h to provide the results, and help to identify diagnosis of psittacosis. Laboratory data showed normal or slightly increased leucocytes, neutrophils, and procalcitonin but high C-reactive protein levels. Computed tomography revealed air-space consolidation and ground-glass opacity, which began in the upper lobe of one lung, and spread to both lungs, along with miliary, nodular, or consolidated shadows. One patient died because of secondary infection with Klebsiella pneumoniae, while the other eight patients experienced complete recoveries.

Conclusions

The use of mNGS can improve accuracy and reduce the delay in diagnosis of psittacosis. Severe psittacosis pneumonia responds well to the timely use of appropriate antibiotics.
Literature
1.
go back to reference Hogerwerf L, De Gier B, Baan B, et al. Chlamydia psittaci (psittacosis) as a cause of community-acquired pneumonia: a systematic review and meta-analysis. Epidemiol Infect. 2017;145:3096–105.CrossRef Hogerwerf L, De Gier B, Baan B, et al. Chlamydia psittaci (psittacosis) as a cause of community-acquired pneumonia: a systematic review and meta-analysis. Epidemiol Infect. 2017;145:3096–105.CrossRef
2.
go back to reference Balsamo G, Maxted AM, Midla JW, et al. Compendium of measures to control chlamydia psittaci infection among humans (Psittacosis) and pet birds (Avian Chlamydiosis), 2017. J Avian Med Surg. 2017;31:262–82.CrossRef Balsamo G, Maxted AM, Midla JW, et al. Compendium of measures to control chlamydia psittaci infection among humans (Psittacosis) and pet birds (Avian Chlamydiosis), 2017. J Avian Med Surg. 2017;31:262–82.CrossRef
3.
go back to reference Charles PG, Whitby M, Fuller AJ, et al. The etiology of community-acquired pneumonia in Australia: why penicillin plus doxycycline or a macrolide is the most appropriate therapy. Clin Infect Dis. 2008;46:1513–21.CrossRef Charles PG, Whitby M, Fuller AJ, et al. The etiology of community-acquired pneumonia in Australia: why penicillin plus doxycycline or a macrolide is the most appropriate therapy. Clin Infect Dis. 2008;46:1513–21.CrossRef
4.
go back to reference Petrovay F, Balla E. Two fatal cases of psittacosis caused by Chlamydophila psittaci. J Med Microbiol. 2008;57:1296–8.CrossRef Petrovay F, Balla E. Two fatal cases of psittacosis caused by Chlamydophila psittaci. J Med Microbiol. 2008;57:1296–8.CrossRef
5.
go back to reference Smith KA, Bradley KK, Stobierski MG, et al. Compendium of measures to control Chlamydophila psittaci (formerly Chlamydia psittaci) infection among humans (psittacosis) and pet birds, 2005. J Am Vet Med Assoc. 2005;226:532–9.CrossRef Smith KA, Bradley KK, Stobierski MG, et al. Compendium of measures to control Chlamydophila psittaci (formerly Chlamydia psittaci) infection among humans (psittacosis) and pet birds, 2005. J Am Vet Med Assoc. 2005;226:532–9.CrossRef
6.
go back to reference Mair-Jenkins J, Lamming T, Dziadosz A, et al. A psittacosis outbreak among english office workers with little or no contact with birds, august 2015. PLoS Curr. 2018;10:646. Mair-Jenkins J, Lamming T, Dziadosz A, et al. A psittacosis outbreak among english office workers with little or no contact with birds, august 2015. PLoS Curr. 2018;10:646.
7.
go back to reference Chau S, Tso EY, Leung WS, et al. Three cases of atypical pneumonia caused by Chlamydophila psittaci. Hong Kong Med J. 2015;21:272–5.CrossRef Chau S, Tso EY, Leung WS, et al. Three cases of atypical pneumonia caused by Chlamydophila psittaci. Hong Kong Med J. 2015;21:272–5.CrossRef
8.
go back to reference Ménard A, Clerc M, Subtil A, et al. Development of a real-time PCR for the detection of Chlamydia psittaci. J Med Microbiol. 2006;55:471–3.CrossRef Ménard A, Clerc M, Subtil A, et al. Development of a real-time PCR for the detection of Chlamydia psittaci. J Med Microbiol. 2006;55:471–3.CrossRef
9.
go back to reference De Gier B, Hogerwerf L, Dijkstra F, et al. Disease burden of psittacosis in the Netherlands. Epidemiol Infect. 2018;146:303–5.CrossRef De Gier B, Hogerwerf L, Dijkstra F, et al. Disease burden of psittacosis in the Netherlands. Epidemiol Infect. 2018;146:303–5.CrossRef
10.
go back to reference Schlaberg R, Chiu CY, Miller S, et al. Validation of metagenomic next-generation sequencing tests for universal pathogen detection. Arch Pathol Lab Med. 2017;141:776–86.CrossRef Schlaberg R, Chiu CY, Miller S, et al. Validation of metagenomic next-generation sequencing tests for universal pathogen detection. Arch Pathol Lab Med. 2017;141:776–86.CrossRef
11.
go back to reference Langelier C, Kalantar KL, Moazed F, et al. Integrating host response and unbiased microbe detection for lower respiratory tract infection diagnosis in critically ill adults. Proc Natl Acad Sci USA. 2018;115:E12353–E1236212362.CrossRef Langelier C, Kalantar KL, Moazed F, et al. Integrating host response and unbiased microbe detection for lower respiratory tract infection diagnosis in critically ill adults. Proc Natl Acad Sci USA. 2018;115:E12353–E1236212362.CrossRef
12.
go back to reference Zhang HC, Ai JW, Cui P, et al. Incremental value of metagenomic next generation sequencing for the diagnosis of suspected focal infection in adults. J Infect. 2019;79:419–25.CrossRef Zhang HC, Ai JW, Cui P, et al. Incremental value of metagenomic next generation sequencing for the diagnosis of suspected focal infection in adults. J Infect. 2019;79:419–25.CrossRef
13.
go back to reference Wang S, Chen Y, Wang D, et al. The feasibility of metagenomic next-generation sequencing to identify pathogens causing tuberculous meningitis in cerebrospinal fluid. Front Microbiol. 2019;10:1993.CrossRef Wang S, Chen Y, Wang D, et al. The feasibility of metagenomic next-generation sequencing to identify pathogens causing tuberculous meningitis in cerebrospinal fluid. Front Microbiol. 2019;10:1993.CrossRef
14.
go back to reference Mandell LA, Wunderink RG, Anzueto A, et al. Infectious diseases society of America/American thoracic society consensus guidelines on the management of community-acquired pneumonia in adults. Clin Infect Dis. 2007;44:S27–72.CrossRef Mandell LA, Wunderink RG, Anzueto A, et al. Infectious diseases society of America/American thoracic society consensus guidelines on the management of community-acquired pneumonia in adults. Clin Infect Dis. 2007;44:S27–72.CrossRef
15.
go back to reference Knittler MR, Sachse K. Chlamydia psittaci: update on an underestimated zoonotic agent. Pathog Dis. 2015;73:1–15.CrossRef Knittler MR, Sachse K. Chlamydia psittaci: update on an underestimated zoonotic agent. Pathog Dis. 2015;73:1–15.CrossRef
16.
go back to reference Sachse K, Bavoil PM, Kaltenboeck B, et al. Emendation of the family Chlamydiaceae: proposal of a single genus, Chlamydia, to include all currently recognized species. Syst Appl Microbiol. 2015;38:99–103.CrossRef Sachse K, Bavoil PM, Kaltenboeck B, et al. Emendation of the family Chlamydiaceae: proposal of a single genus, Chlamydia, to include all currently recognized species. Syst Appl Microbiol. 2015;38:99–103.CrossRef
17.
go back to reference Kohlhoff SA, Hammerschlag MR. Treatment of Chlamydial infections: 2014 update. Expert Opin Pharmaco. 2015;16:205–12.CrossRef Kohlhoff SA, Hammerschlag MR. Treatment of Chlamydial infections: 2014 update. Expert Opin Pharmaco. 2015;16:205–12.CrossRef
18.
go back to reference Beeckman DS, Vanrompay DC. Zoonotic Chlamydophila psittaci infections from a clinical perspective. Clin Microbiol Infect. 2009;15:11–7.CrossRef Beeckman DS, Vanrompay DC. Zoonotic Chlamydophila psittaci infections from a clinical perspective. Clin Microbiol Infect. 2009;15:11–7.CrossRef
19.
go back to reference Donati M, Rodriguez Fermepin M, Olmo A, et al. Comparative in-vitro activity of moxifloxacin, minocycline and azithromycin against Chlamydia Spp. J Antimicrob Chemother. 1999;43:825–7.CrossRef Donati M, Rodriguez Fermepin M, Olmo A, et al. Comparative in-vitro activity of moxifloxacin, minocycline and azithromycin against Chlamydia Spp. J Antimicrob Chemother. 1999;43:825–7.CrossRef
20.
go back to reference Nieuwenhuizen AA, Dijkstra F, Notermans DW, et al. Laboratory methods for case finding in human psittacosis outbreaks: a systematic review. BMC Infect Dis. 2018;18:442.CrossRef Nieuwenhuizen AA, Dijkstra F, Notermans DW, et al. Laboratory methods for case finding in human psittacosis outbreaks: a systematic review. BMC Infect Dis. 2018;18:442.CrossRef
21.
go back to reference Pantchev A, Sting R, Bauerfeind R, et al. New real-time PCR tests for species-specific detection of Chlamydophila psittaci and Chlamydophila abortus from tissue samples. Vet J. 2009;181:145–50.CrossRef Pantchev A, Sting R, Bauerfeind R, et al. New real-time PCR tests for species-specific detection of Chlamydophila psittaci and Chlamydophila abortus from tissue samples. Vet J. 2009;181:145–50.CrossRef
22.
go back to reference Wilson MR, Sample HA, Zorn KC, et al. Clinical metagenomic sequencing for diagnosis of meningitis and encephalitis. N Engl J Med. 2019;380:2327–40.CrossRef Wilson MR, Sample HA, Zorn KC, et al. Clinical metagenomic sequencing for diagnosis of meningitis and encephalitis. N Engl J Med. 2019;380:2327–40.CrossRef
Metadata
Title
Metagenomic next-generation sequencing in the diagnosis of severe pneumonias caused by Chlamydia psittaci
Authors
Xiancheng Chen
Ke Cao
Yu Wei
Yajun Qian
Jing Liang
Danjiang Dong
Jian Tang
Zhanghua Zhu
Qin Gu
Wenkui Yu
Publication date
01-08-2020
Publisher
Springer Berlin Heidelberg
Published in
Infection / Issue 4/2020
Print ISSN: 0300-8126
Electronic ISSN: 1439-0973
DOI
https://doi.org/10.1007/s15010-020-01429-0

Other articles of this Issue 4/2020

Infection 4/2020 Go to the issue