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Legionnaires' disease caused by Legionella pneumophila serogroups 5 and 10, China.

To the Editor: Legionnaires' disease is a systemic infection caused by gram-negative bacteria belonging to the genus Legionella. The primary clinical manifestation is pneumonia. Legionella spp. are typically found in natural and artificially hydrated environments.

Legionella pneumophila is the species responsible for [approximately equal to] 90% of human cases of infection. L. pneumophila is divided into 15 serogroups, among which serogroup 1 is the most prevalent disease-causing variant (1). In contrast, rare cases are caused by other serogroups. We describe a case of Legionnaires' disease caused by co-infection with L. pneumophila serogroups 5 and 10 and the genotype characteristics of these strains.

The case-patient was a 77-yearold man who had chronic hepatitis B for 50 years, ankylosing spondylitis for 40 years, and chronic cholecystitis for 5 years. On September 17, 2012, he was admitted to Wuxi People's Hospital (Wuxi, China) for treatment after a continuous cough for 15 days and a high fever for 2 days. At admission, the patient had a blood pressure of 130/65 mm Hg, a pulse rate of 102 beats/minute, and a body temperature of 37.4[degrees]C, which increased to 38.4[degrees]C four hours later. Laboratory tests showed a leukocyte count of 9,200 cells/[micro]L (88.7% neutrophils) and a C-reactive protein level of 31 mg/L in serum. Lung inflammation was identified by computed tomography. The result of a urinary antigen test for L. pneumophila serogroup 1 (Binax, Portland, ME, USA) was negative. Bronchoalveolar lavage was performed, and fluid was collected for bacterial culture and molecular analysis.

Real-time PCRs were performed with primers specific for the 5S rRNA gene of the genus Legionella (2) and the L. pneumophila-specific mip gene (3). Legionella colonies isolated from bronchoalveolar lavage fluid grew on buffered-charcoal yeast extract agar. Nine Legionella-like colonies were isolated, and all showed positive results by PCRs. The colonies were identified as L. pneumophila serogroups 2-14 by using the Legionella latex test (Oxoid, Basingstoke, UK). Among these colonies, 5 were identified as L. pneumophila serogroup 5, and 4 were identified as serogroup 10 by using a monoclonal antibody (Denka Seiken, Tokyo, Japan). Environmental investigations were conducted in the patient's house and hospital room, but L. pneumophila serogroup 5 and 10 were not detected in any of the locations tested.

Pulsed-field gel electrophoresis (PFGE) (4) was used to investigate the 9 L. pneumophila strains. Two PFGE patterns that were 94% similar were observed; each pattern represented 1 serogroup. The PFGE patterns were compared with those of a reference database of L. pneumophila for China. All L. pneumophila in the database, including 41 strains isolated from the city in which the patient resided in 2012, had patterns different from those of the 9 strains.

Two clinical L. pneumophila strains of different serogroups were further analyzed by sequence typing (5,6). Sequence type (ST) indicated that allele numbers for flaA, pilE, asd, mip, mompS, proA, and neuA genes were 6, 10, 15, 28, 21, 7, and 207 for serogroup 5 strains and 6, 10, 15, 10, 21, 40, and 207 for sero group 10 strains. By querying the ST database for L. pneumophila (http://, we found that both profiles were new and assigned these 2 strains the numbers ST1440 (serogroup 5) and ST1439 (serogroup 10). STs of these 2 isolates differed from each other by only 2 alleles (3 nt in the mip gene and 1 nt in the proA gene), which suggested that the isolates might be more closely related to each other than suggested by serologic analysis.

Human infections with L. pneumophila serogroups 5 and 10 have been rarely reported (1,7). Our study confirms human infection with 2 L. pneumophila serogroups that did not involve serogroup 1. Results for this case-patient also indicated that a negative urinary antigen test result should not be a reason for ruling out Legionnaires' disease because the urinary antigen kit used detects only L. pneumophila serogroup 1 antigen. L. pneumophila serogroups 5 and 10 are probably underrecognized pathogenic serogroups. Culture and molecular analysis should be performed to obtain an accurate diagnosis. Rare co-infections with L. pneumophila serogroup strains have been identified by culture methods (8,9).

The cases reported previously and in this study indicate that co-infections with different serogroups are more common than currently recognized and that multiple colonies should be tested for accurate epidemiologic investigations. Qin et al. reported that pathogenic Legionella strains of different species, serogroups, and genotypes were isolated from the same hot spring water samples (10). This finding suggests that co-infections with different Legionella strains may occur under certain conditions.

In China, Legionnaires' disease is usually ignored in the differential diagnosis of pneumonia because most clinicians lack experience with this disease. This case highlights the need to familiarize physicians with diagnostic methods for identifying Legionella pneumonia in clinics in China and for further epidemiologic surveillance to monitor this disease and improve public health disease control strategies.


We thank the editors and reviewers for providing useful comments.

This study was supported by the Science and Technology Bureau of Wuxi (grant CSE01N1230; The situation of Legionella infection from pneumonia cases and pathogens tracking research) and the Ministry of Health and the Ministry of Science and Technology of the People's Republic of China (grant 2012ZX10004215; the Priority Project on Infectious Disease Control and Prevention).


(1.) Yu VL, Plouffe JF, Castellani-Pastoris M, Stout JE, Schousboe M, Widmer A, et al. Distribution of Legionella species and serogroups isolated by culture in patients with sporadic community-acquired legionellosis: an international collaborative survey. J Infect Dis. 2002;186:127-8.

(2.) Qin T, Hu G, Ren H, Zhu B, Liu Z, Shao Z. Establishment and application of TaqMan real-time PCR in detection of Legionella spp. in environmental water samples [in Chinese]. Zhonghua Yu Fang Yi Xue Za Zhi. 2011;45:444-7.

(3.) Zhang Q, Chen XD, Zhang BY, Qian L, Si CZ, Zhang XZ, et al. Detection of Legionella pneumophila by fluorescence quantitative PCR method [in Chinese]. Jiangsu Journal of Preventive Medicine. 2010; 21:3-6.

(4.) Zhou H, Ren H, Zhu B, Kan B, Xu J, Shao Z. Optimization of pulsed-field gel electrophoresis for Legionella pneumophila subtyping. Appl Environ Microbiol. 2010;76:133 4-40. http://dx.doi. org/10.1128/AEM.01455-09

(5.) Gaia V, Fry NK, Afshar B, Luck PC, Meugnier H, Etienne J, et al. A consensus sequence-based epidemiological typing scheme for clinical and environmental isolates of Legionella pneumophila. J Clin Microbiol. 2005;43:2047-52.

(6.) Ratzow S, Gaia V, Helbig JH, Fry NK, Luck PC. Addition of neuA, the gene encoding N-acylneuraminate cytidylyl transferase, increases the discriminatory ability of the consensus sequencebased scheme for typing Legionella pneumophila serogroup 1 strains. J Clin Microbiol. 2007;45:1965-8. http://dx.doi. org/10.1128/JCM.00261-07

(7.) Amemura-Maekawa J, Kura F, Helbig JH, Chang B, Kaneko A, Watanabe Y, et al. Characterization of Legionella pneumophila isolates from patients in Japan according to serogroups, monoclonal antibody subgroups and sequence types. J Med Microbiol. 2010;59:653-9. http://dx.doi. org/10.1099/jmm.0.017509-0

(8.) Jalaludin BB, Nguyen OT, Goldthorpe IC, Chiew RF. Legionnaires' disease: coinfection with Legionella pneumophila serogroups 1 and 5. Med J Aust. 1997;166:277-8.

(9.) Aubert G, Bornstein N, Rayet I, Pozzetto B, Lenormand PH. Nosocomial infection with Legionella pneumophila serogroup 1 and 8 in a neonate. Scand J Infect Dis. 1990;22:367-70. http://dx.doi. org/10.3109/00365549009027062

(10.) Qin T, Yan G, Ren H, Zhou H, Wang H, Xu Y, et al. High prevalence, genetic diversity and intracellular growth ability of Legionella in hot spring environments. PLoS ONE. 2013;8:e59018. http://dx.doi. org/10.1371/journal.pone.0059018

Address for correspondence: Weijie Zhou, Wuxi Center for Disease Control and Prevention. 499 Jincheng Rd, South Long District, Wuxi City, Jiangsu Province 214023, China; email:

Qi Zhang, [1] Haijian Zhou, [1] Rong Chen, Tian Qin, Hongyu Ren, Bin Liu, Xinliang Ding, Dan Sha, and Weijie Zhou

[1] These authors contributed equally to this article.

Author affiliations: Wuxi Center for Disease Control and Prevention, Wuxi, China (Q. Zhang, R. Chen, B. Liu, X. Ding, D. Sha, W. Zhou); National Institute for Communicable Disease Control and Prevention, Beijing, China (H. Zhou, T. Qin, H. Ren); State Key Laboratory for Infectious Disease Prevention and Control, Beijing (H. Zhou, T. Qin, H. Ren); and Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, Hangzhou, (H. Zhou, T. Qin)

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Article Details
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Title Annotation:LETTERS
Author:Zhang, Qi; Zhou, Haijian; Chen, Rong; Qin, Tian; Ren, Hongyu; Liu, Bin; Ding, Xinliang; Sha, Dan; Zh
Publication:Emerging Infectious Diseases
Article Type:Letter to the editor
Geographic Code:9CHIN
Date:Jul 1, 2014
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