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Antimicrobial Agents and Chemotherapy, April 2003, p. 1447-1448, Vol. 47, No. 4
0066-4804/03/$08.00+0     DOI: 10.1128/AAC.47.4.1447-1448.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.

In Vitro Activity of a New Antibiotic, NVP-PDF386 (VRC4887), against Chlamydia pneumoniae

Patricia M. Roblin and Margaret R. Hammerschlag^*

Division of Infectious Diseases, Department of Pediatrics, State University of New York Downstate Medical Center, Brooklyn, New York 11203-2098

Received 15 July 2002/ Returned for modification 9 November 2002/ Accepted 30 December 2002

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The in vitro activity of NVP-PDF386 (VRC4887), a novel new peptide deformylase inhibitor, and those of levofloxacin and clarithromycin were tested against 21 isolates of Chlamydia pneumoniae. The MIC at which 90% of the isolates were inhibited and the minimal bactericidal concentration at which 90% of the isolates were killed by NVP-PDF386 for all isolates of C. pneumoniae were 0.008 µg/ml (range, 0.008 to 0.015 µg/ml) compared to 0.25 and 0.06 µg/ml for levofloxacin and clarithromycin, respectively.

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Chlamydia pneumoniae is a frequent cause of community-acquired respiratory tract infection, including pneumonia and bronchitis, in adults and children (2). Peptide deformylase (PDF) is a necessary enzyme in bacterial protein synthesis (4). PDF deformylates the N-formylmethionine of newly synthesized polypeptides and represents a novel target for antibacterial chemotherapy. The gene encoding PDF (def) is essential for protein synthesis in a variety of pathogenic bacteria but is not required for mammalian protein synthesis (4). Preliminary studies have shown that PDF inhibitors are active against a wide range of bacterial respiratory pathogens, including Streptococcus pneumoniae, Streptococcus pyogenes, and Moraxella catarrhalis (3; C. Hackbarth, S. Lopez, W. Wang, J. Jacobs, R. Rain, Z. J. Ni, J. Trias, D. Chen, G. Withers, D. V. Patel, and Z. Yuan, Abstr. 40th Intersci. Conf. Antimicrob. Agents Chemother., abstr. 2173, 2000). Data on activity of these compounds against respiratory pathogens responsible for atypical pneumonia, including C. pneumoniae and Mycoplasma pneumoniae, are limited (3). We compared the activity of NVP-PDF386 (VRC4887), a new PDF inhibitor, and those of levofloxacin and clarithromycin against C. pneumoniae.

Isolates of C. pneumoniae tested included two reference isolates, TW183, obtained from the Washington Research Foundation (Seattle, Wash.), and AR39 (ATCC VR-2282); CM-1, a clinical isolate from the Centers for Disease Control and Prevention (ATCC VR-1360); J21, an isolate from Japan; and 17 recent clinical isolates from adults enrolled in a multicenter community-acquired pneumonia treatment study conducted in the United States (isolates 25001, 21001, 21002, 08002, 808016, 22012A, 22012, 24013A, 24013, 493, 453, 124, 490, 600, 912, and 109). NVP-PDF386 (Novartis, Summit, N.J.), levofloxacin (Ortho Pharmaceuticals, Raritan, N.J.), and clarithromycin (Abbott Laboratories, Abbott Park, Ill.) were supplied as drug substances in powder form and were solubilized in accordance with the manufacturers' instructions. Susceptibility testing of C. pneumoniae was performed in cell culture by using HEp-2 cells grown in 96-well microtiter plates as previously described (1, 2). Each experiment was set up in duplicate plates. Each well was inoculated with 0.1 ml of the test organism diluted to yield 10³ to 10⁴ inclusion-forming units/ml for a multiplicity of infection of 1:1; each well was centrifuged at 1,700 x g for 1 h and incubated at 35°C for 1 h. Wells were then aspirated and overlaid with 0.2 ml of medium containing 1 µg of cycloheximide per ml and serial twofold dilutions of the test drug. After incubation at 35°C for 72 h, the cultures in one plate were fixed and stained for inclusions with fluorescein-conjugated antibody to the lipopolysaccharide genus antigen (Pathfinder; Bio-Rad Labs, Hercules, Calif.). The MIC was the lowest antibiotic concentration at which no inclusions were seen. The minimal bactericidal concentration (MBC) was determined by aspirating the antibiotic-containing medium of the second plate, washing wells twice with phosphate-buffered saline, and adding antibiotic-free medium. Cultures were frozen at -70°C, thawed, passed onto fresh new cells, incubated for 72 h, and then fixed and stained as above. The MBC was the lowest antibiotic concentration that resulted in no inclusions after passage. Three replicates were conducted for each assay.

The MICs and MBCs for C. pneumoniae are shown in Table 1. The MIC at which 90% of the strains are inhibited (MIC₉₀) and MBC₉₀ for NVP-PDF386 were 0.008 µg/ml compared to 0.25 and 0.06 µg/ml for levofloxacin and clarithromycin, respectively. The MICs obtained for NVP-PDF386 against C. pneumoniae in the present study were very consistent, especially in view of the wide geographic distribution of the isolates tested.

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TABLE 1. Activity of NVP-PDF 386, levofloxacin, and clarithromycin against 21 isolates of C. pneumoniae

PDF is an interesting bacterial target that was discovered more than 30 years ago but has only recently been exploited. Over the past several years, a number of compounds have been evaluated in vitro and in animal studies. Recently, Wise et al. (3) evaluated the in vitro activity of six PDF compounds, namely, BB-3497, BB-83698, BB-83857, BB-84416, and BB-84518. The MIC₉₀s against S. pneumoniae and Haemophilus influenzae ranged from 0.5 to 6 µg/ml and from 2 to 16 µg/ml, respectively. The compounds were more active against M. catarrhalis, with MIC₉₀s ranging from 0.06 to 0.25 µg/ml. They also tested these compounds against one isolate of C. pneumoniae, TW-183, and two strains of Chlamydia trachomatis. The MICs for C. pneumoniae and C. trachomatis ranged from 0.5 to 2 µg/ml and 0.25 to 4 µg/ml, respectively. BB-83857 appeared to be the most consistently active compound. There are no published data on the activity of NVP-PDF386 against respiratory tract bacteria, although the activity of several related compounds against S. pneumoniae, M. catarrhalis, and H. influenzae appears to be similar to the results reported by Wise et al. (3; Hackbarth et al., 40th ICAAC). In contrast, NVP-PDF386 was extremely active against C. pneumoniae, with an MIC₉₀ of 0.008 µg/ml, which was 7 to 30 times more active than clarithromycin and levofloxacin and 60 to 250 times more active against chlamydia than the PDF compounds studied by Wise et al. (3). The activity of NVP-PDF386 against C. pneumoniae was similar to that found previously with the ketolide ABT-773 and the des-quinolone BMS-284756 (MIC₉₀ for both compounds, 0.015 µg/ml) (1, 2). Preliminary data have also shown that NVP-PDF386 has similar high activity against M. pneumoniae (C. Hackbarth and Z. Yuan, Versicor, personal communication). These data suggest that PDF inhibitors may have a potential role in the treatment of respiratory infections due to C. pneumoniae and other causes of atypical pneumonia.

 
* Corresponding author. Mailing address: Department of Pediatrics, Box 49, SUNY Downstate Medical Center, 450 Clarkson Ave., Brooklyn, NY 11203-2098. Phone: (718) 245-4075. Fax: (718) 245-2118. E-mail: mhammerschlag{at}pol.net.

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1. Malay, S., P. M. Roblin, T. Reznik, A. Kutlin, and M. R. Hammerschlag. 2002. In vitro activity of BMS-28476 against Chlamydia trachomatis and recent clinical isolates of Chlamydia pneumoniae. Antimicrob. Agents Chemother. 46:517-518.[Abstract/Free Full Text]
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2. Strigl, S., P. M. Roblin, T. Reznik, and M. R. Hammerschlag. 2000. In vitro activity of ABT 773, a new ketolide antibiotic, against Chlamydia pneumoniae. Antimicrob. Agents Chemother. 44:1112-1113.[Abstract/Free Full Text]
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3. Wise, R., J. M. Andrews, and J. Ashby. 2002. In vitro activity of peptide deformylase inhibitors against gram-positive pathogens. Antimicrob. Agents Chemother. 46:1117-1118.[Abstract/Free Full Text]
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4. Yuan, Z., J. Trias, and R. J. White. 2001. Deformylase as a novel antibacterial target. Drug Discov. Today 6:954-961.[CrossRef][Medline]

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Antimicrobial Agents and Chemotherapy, April 2003, p. 1447-1448, Vol. 47, No. 4
0066-4804/03/$08.00+0     DOI: 10.1128/AAC.47.4.1447-1448.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.

This article has been cited by other articles:

• Fritsche, T. R., Sader, H. S., Cleeland, R., Jones, R. N. (2005). Comparative Antimicrobial Characterization of LBM415 (NVP PDF-713), a New Peptide Deformylase Inhibitor of Clinical Importance. Antimicrob. Agents Chemother. 49: 1468-1476 [Abstract] [Full Text]  
• Blasi, F. (2004). Atypical pathogens and respiratory tract infections. Eur Respir J 24: 171-182 [Abstract] [Full Text]  

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