Mycobacterium neoaurum contamination.

To the Editor: In reviewing "Rapidly Progressive Dementia due to Mycobacterium neoaurum Meningoencephalitis," by Heckman et al. (1), I found, contrary to the authors' conclusion, that M. neoaurum was more likely a contaminant than a cause. First, within the granulomatous brain lesions, the strongest evidence for the authors' conclusion, no acid-fast bacilli were isolated or identified on special stains; thus, the Koch postulates were not satisfied. Rather, the lesions were likely rheumatoid nodules. Longstanding rheumatoid arthritis commonly causes granulomalike rheumatoid nodules. I did a PubMed search using "rheumatoid nodule in the brain" and 7 articles were found (2,3). A "rheumatoid endarteritis" search found 25 articles. Heckman et al. failed to exclude or discuss this possibility.

Second, M. neoaurum is a rare environmental mycobacterium that grows in [less than or equal to] 2 days on sheep blood agar and is not difficult to culture. As the authors stated, there have been 8 reports of this organism, 7 isolated from blood and 1 from urine. The blood isolates were associated with either central venous catheter or intravenous drug use. Thus, M. neoaurum is of low virulence and unlikely to cause spontaneous infection in tissue unless inoculated accidentally, perhaps. Third, polymerase chain reaction (PCR) is exquisitely sensitive and prone to contamination. The problem is worse when bacterial DNA is amplified by using highly conserved primers. The PCR reagents, from the Taq polymerase (of bacterial origin) to water, contain sufficient, despite minute quantity, bacterial DNA to be amplified (4). Although direct sequencing of the amplicon is often blurry because of its low quantity and mixed content, when cloned, each amplicon may be ligated to the vector and proliferates and gets sequenced later.

Therefore, I believe the presence of M. neoaurum DNA, not the organism itself, represented contamination. Generally, drawing cause-disease conclusion based on PCR sequencing needs vigilance to satisfy the modified Koch postulates (5).

Xiang Y. Han *

* University of Texas, Houston, Texas, USA

References

(1.) Heckman GA, Hawkins C, Morris A, Burrows LL, Bergeron C. Rapidly progressive dementia due to Mycobacterium neoaurum meningoencephalitis. Emerg Infect Dis. 2004;10:924-7.

(2.) Karam NE, Roger L, Hankins LL, Reveille JD. Rheumatoid nodulosis of the meninges. J Rheumatol. 1994;21:1960-3.

(3.) Kim RC, Collins GH. The neuropathology of rheumatoid disease. Hum Pathol. 1981;12:5-15.

(4.) Han XY, Pham AS, Tarrand JJ, Sood PK, Luthra R. Rapid and accurate identification of mycobacteria by sequencing hypervariable regions of the 16S ribosomal RNA gene. Am J Clin Pathol. 2002;118:796-801.

(5.) Fredericks DN, Relman DA. Sequence-based identification of microbial pathogens: a reconsideration of Koch's postulates. Clin Microbiol Rev. 1996;9:18-33.

Address for correspondence: X. Y. Han, Department of Laboratory Medicine, Unit 84, University of Texas, M.D. Anderson Cancer Center, 1515 Holcombe Blvd. Houston 77030, Texas, USA; fax: [phone]: email: [e-mail]

In Response: In response to our report on a case of rapidly progressive dementia (1,2), Dr. Han argues that Mycobacterium neoaurum was "more likely a contaminant than the cause" and that the actual cause of death was most likely rheumatoid pachymeningitis. Dr. Han bases his argument on the absence of positive acid-fast stains or mycobacterial cultures and his assessments that the identification of M. neoaurum DNA was due to contamination and that the pathologic findings represented rheumatoid nodules.

The inability to stain or culture an organism in this case is not unusual, as paucibacillary mycobacterial infections, such as tuberculous lymphadenitis and leprosy, are common (3,4). Though the possibility is not inconceivable, environmental contamination is unlikely, because tissue samples were positive with M. neoaurum specific primers, whereas controls containing identical reagents but no tissue were not.

Dr. Han expresses a valid concern that rheumatoid pachymeningitis was not given due consideration. Rheumatoid pachymeningitis is a rare complication of rheumatoid arthritis, in which patients may exhibit headache, cranial neuropathies, focal deficits, seizures, or cognitive dysfunction (5,6). Rheumatoid pachymeningitis usually, but not exclusively, occurs in patients with long-standing rheumatoid arthritis characterized by erosive disease and extra-articular manifestations, although the systemic disease may be quiescent when neurologic complications arise. Cerebrospinal fluid analysis is generally nonspecific. Magnetic resonance imaging may show prominent meningeal enhancement. Pathologic features may include vasculitis, rheumatoid nodules, and meningeal inflammation, with the latter 2 features being most common (5). The dura may demonstrate inflammation with fibrinoid necrosis (6). We reviewed the pathologic specimens of this case and confirmed the presence of abundant giant cells, endarteritis

proliferans, and, most notably, extensive caseation necrosis typical of mycobacterial infection. We found no evidence of rheumatoid nodules, dural inflammation, or fibrinoid necrosis.

Though this case does not satisfy Koch postulates, neither do most novel infectious diseases. Substantial international efforts were required to satisfy the postulates in the case of SARS (7). In this case, the identification of DNA from a "rare environmental mycobacterium" in a patient with overwhelming pathologic evidence of mycobacterial infection provides strong, though not foolproof, evidence of a possible causal role.

George A. Heckman, * Cynthia Hawkins, ([dagger]) Andrew Morris, ([double dagger]) Lori L. Burrows, ([dagger]) and Catherine Bergeron ([section])

* Chedoke Campus and Freeport Health Centre, Kitchener, Ontario, Canada; ([dagger]) University of Toronto, Toronto, Ontario, Canada; ([double dagger]) McMaster University, Hamilton, Ontario, Canada; ([section]) Toronto Western Hospital, Toronto, Ontario, Canada

References

(1.) Han XY. Mycobacterium neoaurum contamination. Emerg Infect Dis. 2005;11: 1316-7.

(2.) Heckman GA, Hawkins C, Morris A, Burrows LL, Bergeron C. Rapidly progressive dementia due to Mycobacterium neoaurum meningoencephalitis. Emerg Infect Dis. 2004;10:924-7.

(3.) Chao SS, Loh KS, Tan KK, Chong SM. Tuberculous and nontuberculous cervical lymphadenitis: a clinical review. Otolaryngol Head Neck Surg. 2002; 126:176-9.

(4.) Ustianowski AP, Lockwood DNJ. Leprosy: current diagnostic and treatment approaches. Cur Opin Infect Dis. 2003;16:421-7.

(5.) Kato T, Hoshi K, Sekijima Y, Matsuda M, Hashimoto T, Otani M, et al. Rheumatoid meningitis: an autopsy report and review of the literature. Clin Rheumatol. 2003;22: 475-80.

(6.) Tan HJ, Raymond AA, Phadke PP, Rozman Z. Rheumatoid pachymeningitis. Singapore Med J. 2004;45:337-9.

(7.) Osterhaus ADME, Fouchier RAM, Kuiken T. The aetiology of SARS: Koch's postulates fulfilled. Philos Trans R Soc Lond B Biol Sci. 2004;359:1081-2.

Address for correspondence: George A. Heckman, Department of Medicine, Hamilton Health Sciences, Chedoke Campus and Freeport Health Centre, 3570 King Street East, Kitchener, Ontario, Canada, N2C 2W1: fax: [phone]: email: [e-mail]