41
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Legionnaires’ Disease Caused by Legionella pneumophila Serogroups 5 and 10, China

      letter

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          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 ≈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-year-old 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°C, which increased to 38.4°C four hours later. Laboratory tests showed a leukocyte count of 9,200 cells/μL (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 serogroup 10 strains. By querying the ST database for L. pneumophila (http://www.ewgli.org), 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.

          Related collections

          Most cited references8

          • Record: found
          • Abstract: found
          • Article: not found

          Distribution of Legionella species and serogroups isolated by culture in patients with sporadic community-acquired legionellosis: an international collaborative survey.

          This international collaborative survey identified culture-confirmed legionellosis in 508 patients with sporadic community-acquired legionellosis. Legionella pneumophila constituted 91.5% of the isolates. Serogroup 1 was the predominant serogroup (84.2%), and serogroups 2-13 (7.4%) accounted for the remaining serogroups. The Legionella species most commonly isolated were L. longbeachae (3.9%) and L. bozemanii (2.4%), followed by L. micdadei, L. dumoffii, L. feeleii, L. wadsworthii, and L. anisa (2.2% combined). L. longbeachae constituted 30.4% of the community-acquired Legionella isolates in Australia and New Zealand.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Consensus sequence-based scheme for epidemiological typing of clinical and environmental isolates of Legionella pneumophila.

            A previously described sequence-based epidemiological typing method for clinical and environmental isolates of Legionella pneumophila serogroup 1 was extended by the investigation of three additional gene targets and modification of one of the previous targets. Excellent typeability, reproducibility, and epidemiological concordance were determined for isolates belonging to both serogroup 1 and the other serogroups investigated. Gene fragments were amplified from genomic DNA, and PCR amplicons were sequenced by using forward and reverse primers. Consensus sequences are entered into an online database, which allows the assignment of individual allele numbers. The resulting sequence-based type or allelic profile comprises a string of the individual allele numbers separated by commas, e.g., 1,4,3,1,1,1, in a predetermined order, i.e., flaA, pilE, asd, mip, mompS, and proA. The index of discrimination (D) obtained with these six loci was calculated following analysis of a panel of 79 unrelated clinical isolates. A D value of > 0.94 was obtained, and this value appears to be sufficient for use in the epidemiological investigation of outbreaks caused by L. pneumophila. The D value rose to 0.98 when the results of the analysis were combined with those of monoclonal antibody subgrouping. Sequence-based typing of L. pneumophila is epidemiologically concordant and discriminatory, and the data are easily transportable. This consensus method will assist in the epidemiological investigation of L. pneumophila infections, especially travel-associated cases, by which it will allow a rapid comparison of isolates obtained in more than one country.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Addition of neuA, the gene encoding N-acylneuraminate cytidylyl transferase, increases the discriminatory ability of the consensus sequence-based scheme for typing Legionella pneumophila serogroup 1 strains.

              The standard sequence-based method for the typing of Legionella pneumophila serogroup 1 strains was extended by using the gspA and neuA alleles. The use of neuA as a seventh allele for typing significantly increased the index of discrimination calculated for a panel of unrelated strains (from 0.932 to 0.963) and subdivided some known large common complexes (e.g., 1,4,3,1,1,1). This modification to the standard method is proposed as the method of choice in the epidemiological investigation of L. pneumophila infections.
                Bookmark

                Author and article information

                Journal
                Emerg Infect Dis
                Emerging Infect. Dis
                EID
                Emerging Infectious Diseases
                Centers for Disease Control and Prevention
                1080-6040
                1080-6059
                July 2014
                : 20
                : 7
                : 1242-1243
                Affiliations
                [1]Wuxi Center for Disease Control and Prevention, Wuxi, China (Q. Zhang, R. Chen, B. Liu, X. Ding, D. Sha, W. Zhou);
                [2]National Institute for Communicable Disease Control and Prevention, Beijing, China (H. Zhou, T. Qin, H. Ren);
                [3]State Key Laboratory for Infectious Disease Prevention and Control, Beijing (H. Zhou, T. Qin, H. Ren);
                [4]Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, Hangzhou, (H. Zhou, T. Qin)
                Author notes
                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: wxcdczwj@ 123456163.com
                Article
                13-1343
                10.3201/eid2007.131343
                4073842
                24964208
                871913ad-ed36-462a-b3e7-c07804facd6a
                History
                Categories
                Letters to the Editor
                Letter

                Infectious disease & Microbiology
                legionnaires’ disease,legionella pneumophila,bacteria,serogroup 5,serogroup 10,co-infection,pneumonia,china

                Comments

                Comment on this article