X-ray of Pneumocystis jiroveci pneumonia There is increased white (opacity) in the lower lungs on both sides, characteristic of Pneumocystis pneumonia
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Pneumocystis jiroveci pneumonia

Pneumocystis jiroveci pneumonia or Pneumocystis pneumonia (PCP) is a form of pneumonia caused by a yeast-like fungal microorganism called Pneumocystis jiroveci (sometimes spelled jirovecii, formerly known as Pneumocystis carinii). It is relatively rare in people with normal immune systems but common among people with AIDS. PCP can also develop in patients who are taking immunosuppressant medications (e.g., patients who have undergone solid organ transplantion) and in patients who have undergone bone marrow transplantation. more...

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Symptoms

Symptoms of PCP include high fever, non-productive cough, shortness of breath (especially on exertion), weight loss and night sweats. There is usually not a large amount of sputum with PCP unless the patient has an additional bacterial infection. The fungus can invade other visceral organs, such as the liver, spleen and kidney, but only in a minority of cases.

Diagnosis

The clinical diagnosis can be confirmed by the characteristic appearance of the chest x-ray which shows widespread pulmonary infiltrates, and an arterial oxygen level (pO2) strikingly lower than would be expected from symptoms. The diagnosis can be definitively confirmed by pathologic identification of the causative organism in induced sputum or bronchial washings obtained by bronchoscopy with coloration by toluidine blue or immunofluorescence assay.

PCP and AIDS

Because PCP rarely occurs without AIDS, it can be one of the first clues to a new AIDS diagnosis, though it does not generally occur unless the CD4 count is less than 200/mm³. An unusual rise in PCP cases in North America, noticed when physicians began requesting large quantities of the rarely used antibiotic pentamidine, was the first clue to the existence of AIDS in the early 1980s.

Prior to the development of more effective treatments, PCP was a common and rapid cause of death in AIDS patients. Much of the incidence of PCP has been reduced by instituting a standard practice of using oral trimethoprim/sulfamethoxazole to prevent the disease in people with CD4 counts less than 200/mm³. In populations that do not have access to preventative treatment, PCP continues to be a major cause of death in AIDS.

Treatments

Antipneumocystic medication is used with concomitant steroids in order to avoid inflammation, which causes an exacerbation of symptoms about four days after treatment begins if steroids are not used. By far the most commonly used medication is a combination of trimethoprim and sulfamethoxazole (co-trimoxazole, with the tradenames Bactrim, Septrin, or Septra), but some patients are unable to tolerate this treatment due to allergies. Other medications that are used, alone or in combination, include pentamidine, trimetrexate, dapsone, atovaquone, primaquine, and clindamycin. Treatment is usually for a period of about 21 days.

Nomenclature

The name P. jiroveci, to distinguish the organism found in humans from variants of Pneumocystis found in other animals, was first proposed in 1976, in honor of Otto Jirovec, who described Pneumocystis pneumonia in humans in 1952. After DNA analysis showed significant differences in the human variant, the proposal was made again in 1999 and has come into common use; P. carinii still describes the species found in rats. The International Code of Botanical Nomenclature would normally require the name to be spelled jirovecii rather than jiroveci; both spellings are currently in use.

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A new name for Pneumocystis from human - Pneumocystis jiroveci - Letters - response to W.T. Hughes
From Emerging Infectious Diseases, 2/1/03 by James R. Stringer

Reply to W.T. Hughes: We appreciate Dr. Hughes' letter of concern regarding our article endorsing the name Pneumocystis jiroveci (1). When working with well-known disease agents and syndromes, these types of changes are more difficult to adopt because of the effect they have on daily communication, patient care, record keeping, and other important routines of health-care providers. However, in this case, new information and understanding dictate that a change be made.

For some time, scientists have known that humans are infected by a particular species of Pneumocystis and that this species does not infect other host species. In recognition of these facts, Frenkel named the human pathogen Pneumocystis jiroveci, using the procedure prescribed by the International Code of Botanical Nomenclature (ICBN) (2). Although Dr. Hughes raised a number of issues, none justifies rejecting the new, valid name.

Dr. Hughes suggested that the name P. jiroveci is incorrect on the basis of principal III of ICBN, which holds that "the nomenclature of a taxonomic group is based upon priority of publication." He indicated that Jirovec was not the first investigator to report Pneumocystis in humans. Although this situation may be the case, principal III has not been violated because "priority of publication" refers to the time when a name is validly published, not to the time when an organism is first described. The name P jiroveci was validly published in 1999, and this name therefore has priority. To be valid, all of the following steps must be completed: a name must be published in a scientific journal, the name must be a binary Latin name, the organism must be described in Latin, the rank of the organism must be indicated, and the new species must be called by the term "typus or holotypus," and the specimen or microscope slides must be placed in a public holding (details are available from: URL: http:// www.bgbm.fu-berlin.de/iapt/nomenclature/code/SaintLouis/0000St.Luistitle.htm). Dr. Frenkel was the first to fulfill these requirements in his 1999 publication (2).

The 1912 publication by Delanoe and Delanoe does not have priority in naming Pneumocystis from humans because the organism studied by the Delanoes was from the rat. The rat-derived Pneumocystis organism continues to be known as P. carinii, in keeping with principal III. As an additional historical note, Dr. Frenkel was the first investigator to understand the clear differences between human and rat-derived Pneumocystis, which were described in a landmark publication in 1976 (3). He proposed a change in nomenclature in which the name Pneumocystis jiroveci n. sp. applied to the human organisms and Pneumocystis carinii was retained for the rat organism. However, Frenkel did not attempt to follow ICBN procedures because at the time Pneumocystis was thought to be a protozoan. Nevertheless, this early paper established the idea of naming human Pneumocystis, P. jiroveci.

Dr. Hughes stated a concern over the possibility that the name change may cause "confusion and undue anxiety among the many thousands of HIV-infected patients who attend clinics." Such concern is understandable. However, patients will have guidance in understanding the significance of the name change. Health-care providers will allay any fears that might be elicited by the application of the new name. The level of anxiety experienced by persons at risk of acquiring Pneumocystis carinii pneumonia (PCP) is more likely to decline than to increase. People may be relieved to learn that they are not going to catch PCP from a pet, for example.

Dr. Hughes suggested that the name P jiroveci is unofficial because it has not yet been sanctioned by a body of experts that scrutinizes proposed name changes and has the power to either accept or reject them. This situation is not the case. The process by which new names are validated does not directly involve a body of experts. The International Botanical Congress does not evaluate names. Instead, the congress has established ICBN, which sets forth the procedures authors must follow to publish a valid new name. The scientific basis for the new name is included in the publication. In the case of P. jiroveci, abundant evidence shows that P. carinii and P. jiroveci are different species. This evidence, which also indicates that the genus Pneumocystis contains many additional species, has been reviewed extensively (4,5). Dr. Hughes gave the impression that that this evidence is exclusively molecular genetic data. In fact, the molecular genetic evidence is mirrored by clear biologic differences, the most dramatic being host species specificity.

As our knowledge of the biology and genetics of disease-causing microorganisms grows, openness to changes in the taxonomy and classification is needed. Given the impact such changes can have outside of the realm of basic science, the decision to accept the proposed changes in the nomenclature used for Pneumocystis has not been made frivolously. This decision is the result of a long and deliberate process that began almost 10 years ago, when data demonstrating that different mammalian hosts harbor different Pneumocystis species first began to appear. In 1994 and 2001, nomenclature issues were discussed at international meetings of the Pneumocystis community, with both physicians and research investigators present. In 1994, the data supporting new species were relatively limited. Consequently, a provisional tripartite nomenclature was adopted in lieu of recognizing new species (6). By 2001, however, the existence of multiple species and the necessity of assigning new species names were accepted by consensus. Because Frenkel had already published the name P. jiroveci, the suitability and validity of this name were also discussed. The new name was approved by consensus (4). We recognize that the results of these meetings do not necessarily reflect all opinions on the matter of Pneumocystis nomenclature, but we know of no better way to assess the majority opinion.

In endorsing the name Pneumocystis jiroveci, we hope to foster scientific understanding and communication. The tripartite name formerly used to denote the distinctness of this organism is not only cumbersome, it is inadequate because its meaning is not apparent and must be defined every time it is used. The arcane nature of the tripartite name tended to deprive the broad audience of persons interested in PCP of vital information, namely, a unique species of Pneumocyctis infects humans. By contrast, the new species name clearly states the uniqueness of P. jiroveci; a distinction is needed when assessing the significance of findings obtained by studies on other members of the genus. Recognition of this uniqueness will undoubtedly stimulate more research on this species. Communication will best be served by uniformity in nomenclature.

Frenkel has assigned a valid name to the Pneumocystis species found in humans. Ignoring this name on the grounds of inconvenience is not only unjustified, it is impractical. If names published in accordance with ICBN are not accepted, the field will have no recognized mechanism for conferring names, fostering the use of idiosyncratic, inadequate, and misleading names. Communication and progress will suffer as a result.

James R. Stringer, * Charles Ben Beard, ([dagger]) Robert F. Miller, ([double dagger]) and Melanie T. Cushion *

* University of Cincinnati, Cincinnati, Ohio, USA; ([dagger]) Centers for Disease Control and Prevention, Atlanta, Georgia, USA; and ([double dagger]) University College London, London, U.K.

References

(1.) Stringer JR, Beard CB, Miller RF, Wakefield AE. A new name (Pneumocystis jiroveci) for Pneumocystis from humans. Emerg Infect Dis 2002;8:891-6.

(2.) Frenkel JK. Pneumocystis pneumonia, an immunodeficiency-dependent disease (IDD): a critical historical overview. J Eukaryot Microbiol 1999;46:89S-92.

(3.) Frenkel JK. Pneumocystis jiroveci n. sp. from man: morphology, physiology, and immunology in relation to pathology. National Cancer Institute Monographs 1976;43:13-30.

(4.) Stringer JR, Cushion MT, Wakefield AE. New nomenclature for the genus Pneumocystis. Supplement: Proceedings of the Seventh International Workshops on Opportunistic Protists, Cincinnati, Ohio, June 13-16, 2001. J Eukaryot Microbiol 2001;Suppl: 184s-9.

(5.) Wakefield AE, Stringer JR, Tamburrini E, Dei-Cas E. Genetics, metabolism and host specificity of Pneumocystis carinii. Med Mycol 1998;36:183-93.

(6.) Revised nomenclature for Pneumocystis carinii. The Pneumocystis Workshop. J Eukaryot Microbiol 1994;41:121 S-2.

Address for correspondence: James R. Stringer, Department of Molecular Genetics, Biochemistry and Microbiology, College of Medicine, University of Cincinnati, ML 524, 231 Albert Sabin Way, Cincinnati, OH 45267, USA; fax: 513-558-8474; e-mail: stringjr@ucmail.uc.edu

COPYRIGHT 2003 U.S. National Center for Infectious Diseases
COPYRIGHT 2003 Gale Group

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