Volume 10, Number 10—October 2004
Dihydropteroate Synthase Gene Mutations in Pneumocystis and Sulfa Resistance
Dihydropteroate Synthase Mutations in Pneumocystis
Association of Sulfamethoxazole and Dapsone with DHPS Gene Mutations
Lack of Association of Trimethoprim with DHFR Gene Mutations
Clinical Importance of DHPS Gene Mutations in P. jirovecii
Summary and Future Directions
Cite This Article
Pneumocystis pneumonia (PCP) remains a major cause of illness and death in HIV-infected persons. Sulfa drugs, trimethoprim-sulfamethoxazole (TMP-SMX) and dapsone are mainstays of PCP treatment and prophylaxis. While prophylaxis has reduced the incidence of PCP, its use has raised concerns about development of resistant organisms. The inability to culture human Pneumocystis, Pneumocystis jirovecii, in a standardized culture system prevents routine susceptibility testing and detection of drug resistance. In other microorganisms, sulfa drug resistance has resulted from specific point mutations in the dihydropteroate synthase (DHPS) gene. Similar mutations have been observed in P. jirovecii. Studies have consistently demonstrated a significant association between the use of sulfa drugs for PCP prophylaxis and DHPS gene mutations. Whether these mutations confer resistance to TMP-SMX or dapsone plus trimethoprim for PCP treatment remains unclear. We review studies of DHPS mutations in P. jirovecii and summarize the evidence for resistance to sulfamethoxazole and dapsone.
Although decreasing in incidence as a result of combination antiretroviral therapy and effective prophylaxis, Pneumocystis pneumonia (PCP), caused by Pneumocystis jirovecii (formerly P. carinii f. sp. hominis), remains the most common AIDS-defining opportunistic infection, as well as the most frequent serious opportunistic infection in HIV-infected persons, in the United States and Europe. Despite the fact that this infection can be prevented, certain patients continue to be at increased risk for PCP. Specifically, PCP frequently signals HIV infection in patients not previously known to be HIV-infected (1). Patients who are not receiving regular medical care, as well as those who are not receiving or responding to antiretroviral therapy or prophylaxis, are also at increased risk for PCP (2). PCP may also develop in other immunosuppressed populations, such as cancer patients and transplant recipients. Furthermore, PCP remains a leading cause of death among critically ill patients, despite advances in treatment and management (3).
The first-line treatment and prophylaxis regimen for PCP is trimethoprim-sulfamethoxazole (TMP-SMX) (4). While prophylaxis has been shown to reduce the incidence of PCP, the widespread and long-term use of TMP-SMX in HIV patients has raised concerns regarding the development of resistant organisms. Even short-term exposure to TMP-SMX can be associated with the emergence of TMP-SMX resistance, as has been demonstrated in patients with acute cystitis caused by Escherichia coli (5). Indeed, an increased number of sulfa-resistant bacteria have been isolated in HIV patients, which coincides with the rise in TMP-SMX prophylaxis for PCP (6,7). In one study, the prevalence of TMP-SMX–resistant Staphylococcus aureus and Enterobacteriaceae species isolated in all hospitalized patients increased significantly from <5.5% of isolates before 1986 to 20% in 1995, during which time TMP-SMX prophylaxis was increasing in HIV-infected patients (6). In addition, the rise in resistant organisms was significantly more prominent in samples obtained from HIV-infected patients, in whom resistant isolates increased from 6.3% in 1988 to 53% in 1995. Another study found that significantly more TMP-SMX–resistant organisms were isolated from HIV-infected patients who had received TMP-SMX than from patients who had not received TMP-SMX (7).
Given the emergence of resistance to TMP-SMX among many bacteria (8), concern has focused on the potential development of resistant Pneumocystis. Based on animal studies, nearly all of the anti-Pneumocystis activity of TMP-SMX is due to sulfamethoxazole (9). The development of sulfonamide resistance could result in the failure of sulfamethoxazole as well as dapsone, a sulfone antimicrobial agent also used in the treatment and prophylaxis of PCP. While separate lines of investigation also suggest that Pneumocystis may be developing resistance to atovaquone, a second-line PCP treatment and prophylaxis regimen (10), we concentrate our review on the evidence for the development of sulfonamide-resistant Pneumocystis.
Sulfonamides act by interfering with folate synthesis. Since many microorganisms cannot transport folate into cells as mammalian cells can, most prokaryotes and lower eukaryotes must synthesize folates de novo (11). Sulfonamides inhibit one of the integral enzymes in folate synthesis, dihydropteroate synthase (DHPS), which catalyzes the condensation of para-aminobenzoic acid and pteridine to form dihydropteroic acid (Figure). Since mammalian cells lack DHPS, sulfonamides can selectively inhibit the growth of various microorganisms. Trimethoprim, part of the fixed combination TMP-SMX, inhibits another of the integral enzymes, the dihydrofolate reductase (DHFR).
Resistance to sulfonamides can emerge by means of a number of mechanisms (12). In most gram-negative enteric bacteria, sulfonamide resistance is largely plasmid-borne and related to drug-resistant DHPS variants with substantial sequence divergence (12). Chromosomal mutations in the DHPS locus—such as point mutations, insertions of duplicate amino acids, or larger sequence alterations as a result of recombination—can also lead to resistance (8). In some organisms, several different mechanisms of resistance have been identified in different strains. For example, some strains of Neisseria meningitidis have acquired a DHPS gene with 10% sequence divergence, postulated by others to be due to recombination (12), whereas other Neisseria strains have acquired a chromosomal insertion, resulting in the addition of two amino acids to DHPS (13). In other organisms, such as E. coli and Plasmodium falciparum, nonsynonymous point mutations resulting in amino acid substitutions in DHPS can confer sulfa resistance (14,15). Furthermore, the accumulation of additional mutations over time can confer increasing levels of sulfa resistance, as has occurred in P. falciparum (16).
Similar to other microorganisms, mutations have been identified in the DHPS gene of P. jirovecii, which has raised the question of whether P. jirovecii is developing resistance to sulfonamides. The DHPS gene of P. jirovecii has been sequenced and is part of the folic acid synthesis gene or fas gene; it encodes a trifunctional protein along with dihydroneopterin aldolase and hydroxymethyldihydropterin pyrophosphokinase (17). Sulfa medications appear to exert selective pressure on Pneumocystis (18), as the DHPS gene is more likely to display mutations in highly conserved regions in patients with PCP who have previously been exposed to sulfa medications (19–25). These DHPS gene mutations were rarely found in clinical isolates before the early 1990s (19,20,22). Genetic analysis suggests that the mutations arose independently in multiple strains of Pneumocystis, which supports the theory that exposure to sulfa medications selects for DHPS gene mutations (26). Furthermore, DHPS gene mutations have not been found in other mammalian Pneumocystis species that have not been exposed to sulfa medications (18,27).
Several factors suggest that the mutations observed in P. jirovecii may confer resistance to sulfa medications. The region of the DHPS gene in which mutations have been identified is one that is highly conserved among other organisms, including Plasmodium falciparum, Streptococcus pneumoniae, E. coli, and Bacillus subtilis (18). The most common mutations identified in the Pneumocystis jirovecii DHPS are nonsynonymous point mutations, which result in amino acid substitutions at positions 55, 57, or both. Different strains with single or double amino acid substitutions at these positions have been identified (Table 1). Based on homology to the E. coli DHPS, these point mutations appear to be in an active site of the enzyme involved in substrate binding; thus, amino acid substitutions in these regions could result in structural changes that could interfere with substrate binding and enzyme activity (21). Likewise, similar point mutations in positions equivalent to this site in Plasmodium falciparum (15) and Mycobacterium leprae (28) confer sulfa resistance. Other mutations near this site also cause sulfa resistance in S. pneumoniae and P. falciparum (29).
However, the inability to reliably culture P. jirovecii in a standardized in vitro culture system prevents the routine susceptibility testing of Pneumocystis. The lack of a standardized culture system also hampers research into the development and testing of new antimicrobial agents with anti-Pneumocystis activity, which highlights our reliance on TMP-SMX as the current mainstay of therapy. Thus, the clinical significance of these DHPS gene mutations must be inferred from correlating the clinical outcome with the presence of DHPS gene mutations in patients with PCP.
Several studies have consistently demonstrated a significant association between the use of TMP-SMX or dapsone for PCP prophylaxis in HIV-infected persons and the presence of DHPS gene mutations (Table 2) (19–25,30). One study extended these findings to the use of pyrimethamine plus sulfadoxine for PCP prophylaxis (29). Another study demonstrated an apparent reversal of the DHPS mutant-to-wild-type ratios after the use of TMP-SMX was restricted (31). In total, studies report >700 episodes of PCP, span a period from 1976 to 2001, and include patient data and clinical specimens from multiple cities in several different countries. Unfortunately, these studies used different criteria to define PCP prophylaxis with TMP-SMX or dapsone, which effectively limits attempts at data pooling for more direct and detailed analyses. In addition, most of the studies collected data by abstracting information from patient charts. Thus, these studies were unable to assess whether patients adhered to the prescribed prophylaxis. Nevertheless, seven of the nine studies found that most HIV-infected patients with a diagnosis of PCP who had been prescribed TMP-SMX or dapsone for PCP prophylaxis had Pneumocystis that contained DHPS mutations (range 19%–80%, Table 2) (19–24,29). Furthermore, eight of the nine studies reported that PCP patients for whom TMP-SMX or dapsone was prescribed were more likely to have Pneumocystis that contained DHPS mutations than were patients for whom these medications were not prescribed (10–25,29).
Of note, in all nine studies, DHPS mutations were observed in PCP patients who were not currently receiving TMP-SMX or dapsone. Whether these patients who failed to meet the defined criteria for TMP-SMX or dapsone prophylaxis had ever received one of these medications for prophylaxis or had received TMP-SMX for a reason other than PCP prophylaxis at some point during their lives was difficult to assess with any degree of confidence. Nevertheless, most of the studies found that only a minority of PCP patients who had not been prescribed TMP-SMX or dapsone for PCP prophylaxis had Pneumocystis that contained DHPS mutations. The study that reported the highest proportion (48%) used both chart abstraction and patient interview as sources of clinical information regarding PCP prophylaxis (23). This study also used a broad definition of PCP prophylaxis, including patient report of TMP-SMX use for prophylaxis at any time in life. Thus, despite rigorous attempts to document TMP-SMX or dapsone use for PCP prophylaxis and with the broadest definition of prophylaxis applied, nearly half of the patients without TMP-SMX or dapsone use had evidence of DHPS mutations on their clinical PCP specimen. Among the 26 patients with a new diagnosis of HIV infection at the time PCP was diagnosed and who thus had never received PCP prophylaxis, 14 (54%) had Pneumocystis that contained DHPS gene mutations. The specific city of residence was also an independent predictor associated with the risk for Pneumocystis that contained DHPS gene mutations. Patients who lived in San Francisco were five times more likely, and patients who lived in Seattle were more than three times as likely to have mutant DHPS than patients who resided in Atlanta, even when factors including sulfonamide or dapsone PCP prophylaxis and prior PCP were controlled for. The presence of DHPS mutations in patients without prior TMP-SMX or dapsone use for PCP prophylaxis, the absence of similar mutations in Pneumocystis isolated from other mammalian species, and the impact of geography on DHPS genotype have substantial implications for disease transmission (i.e., person-to-person transmission) that are beyond the scope of this review (32–35).
Trimethoprim inhibits another of the integral enzymes in folate synthesis, DHFR (Figure). In other microorganisms, point mutations in the DHFR gene are an important mechanism of drug resistance. This finding has led researchers to examine the DHFR gene of P. jirovecii to evaluate whether DHFR mutations contribute to TMP-SMX resistance. To date, two studies have failed to demonstrate an association between the use of TMP-SMX for PCP prophylaxis in HIV-infected persons and the presence of DHFR gene mutations (21,36). In one study, 36 of 37 specimens (from 35 patients, 26 of whom were HIV-infected) demonstrated identical DHFR sequences, with a single specimen showing one synonymous nucleotide change (21). In the second study, 16 (59%) of 27 specimens (from 27 patients, 19 of whom were HIV-infected) had DHFR gene mutations, 14 had synonymous changes, and 2 had nonsynonymous changes (36). Neither of the two patients whose PCP specimen had nonsynonymous DHFR changes had prior exposure to DHFR inhibitors, yet both patients were treated successfully for PCP with TMP-SMX. In addition, this study aligned the Pneumocystis DHFR sequences with those of E. coli, Staphylococcus aureus, Streptococcus pneumoniae, and Plasmodium falciparum and reported that the observed nonsynonymous changes in Pneumocystis DHFR were not in the highly conserved regions of the enzyme as are the amino acid substitutions that confer resistance to TMP (or pyrimethamine) in these other organisms. Thus, the presence and association of DHPS, but not DHFR, gene mutations with the use of specific PCP prophylaxis regimens argue strongly both for the importance of SMX and dapsone against Pneumocystis and the central role of DHPS mutations in the potential development of TMP-SMX or dapsone resistance.
A number of studies have examined the effect of DHPS gene mutations on clinical outcomes such as death, death specifically attributable to PCP, and PCP treatment failure with TMP-SMX or dapsone plus trimethoprim (Table 3) (19–22,24,25,37–39). Whether the presence of DHPS gene mutations confers clinical resistance to TMP-SMX or dapsone plus trimethoprim for PCP treatment remains unclear and requires further study. In a multivariate analysis, Helweg-Larsen and colleagues found that DHPS mutations were an independent predictor associated with increased death rates (20). In this study, DHPS mutation was the strongest predictor of death, and patients who had Pneumocystis that contained DHPS mutations had a greater than threefold increased risk for death within 3 months compared to patients with the wild-type DHPS, after important mortality cofactors such as age, CD4-cell count, and arterial oxygen partial pressure (PaO2) were controlled for. Whether this increased death rate was due to failure of TMP-SMX for PCP treatment is unclear. In fact, 12 (63%) of 19 PCP patients with Pneumocystis that contained DHPS gene mutations responded to PCP treatment with TMP-SMX. Kazanjian and co-workers found that the presence of DHPS mutations was associated with an increased risk for PCP treatment failure with TMP-SMX or dapsone plus trimethoprim (22). In univariate analysis, PCP patients who had Pneumocystis that contained DHPS gene mutations had a greater than twofold increased risk for treatment failure with one of these regimens, compared to patients with the wild-type DHPS. In this study, treatment failure was defined as worsening of clinical features after 7 days of therapy, failure to improve after 10 days of therapy, or a change in therapy because the treating physician perceives failure. Patients who responded clinically to therapy but who switched therapies because of adverse effects were considered to have been treated successfully. Similar to the findings of Helweg-Larsen, most patients with Pneumocystis that contained DHPS gene mutations responded to PCP treatment with TMP-SMX or dapsone plus trimethoprim. Overall, 15 (71%) of 21 PCP patients with Pneumocystis that contained DHPS gene mutations responded to PCP treatment with one of these two regimens. In addition, this study found no association between the presence of DHPS mutations and death at 4 weeks. In contrast to these prior two studies, Navin and colleagues found no association between the presence of DHPS mutations and overall number of deaths at 6 weeks, death attributable specifically to PCP, or PCP treatment failure (39). Overall, 16 (17%) of 94 PCP patients with DHPS mutations died compared to 9 (25%) of 36 PCP patients with wild-type DHPS (p = 0.30). Similarly, seven patients (7%) with PCP with DHPS mutations died as a result of PCP compared to four patients (11%) with wild-type DHPS. Among the 66 patients with PCP with DHPS mutations who were treated with TMP-SMX, 56 (85%) responded to this treatment. In this study, patients were classified as having been successfully treated if they completed a full course of therapy and responded or if they responded sufficiently to be switched from intravenous to oral therapy and be discharged. Similar to the Kazanjian study, patients who responded clinically to therapy but who switched therapies because of adverse effects were considered to have been treated successfully. This noted TMP-SMX response rate was significantly better than the rate for patients with DHPS mutation who were treated with intravenous pentamidine or clindamycin plus primaquine (14 [50%] of 28) and for patients with the wild-type DHPS who were treated with TMP-SMX (23 [64%] of 36). These results were similar when the analysis was restricted to patients who had been treated for at least 7 days with their initial therapy. Although these three patient groups did not differ in terms of age, CD4-cell count, serum albumin, serum lactate dehydrogenase (LDH), or proportion who required corticosteroids, no multivariate analysis was performed to determine independent predictors associated with death (or PCP treatment failure). Instead, a series of stratified analyses were performed and failed to detect any subsets of PCP patients in whom DHPS mutations were associated with a worse outcome.
Whether Pneumocystis DHPS gene mutations confer clinical resistance to TMP-SMX or dapsone plus trimethoprim for PCP treatment remains unclear. Published studies offer conflicting results. Each study used different definitions for PCP prophylaxis and PCP treatment success or failure, and each examined patient deaths at different time-points, with different methods of statistical analysis. These methodologic differences limit attempts at data pooling for more direct and detailed analyses. The outcome of HIV-infected patients with PCP is a complex issue, with multiple factors affecting death, including those related to the patient (e.g., age), the patient’s overall health status (e.g., serum albumin), the underlying HIV/AIDS (e.g., coexisting opportunistic infections or conditions), and, of course, those specific factors related to PCP (e.g., disease severity, presence of respiratory failure, need for mechanical ventilation, and development of serious complications such as pneumothorax). In each individual report, the overall number of patients studied and the subset of patients who had Pneumocystis that contained DHPS mutations and were treated with TMP-SMX or dapsone plus trimethoprim were too small to account for these factors and to detect small differences in outcome that may be related to drug resistance. Furthermore, these and future observational studies that examine DHPS genotype and PCP treatment outcome are complicated by the absence of validated PCP clinical treatment guidelines, practice standards, and definitions of treatment success or failure.
While the declining incidence of PCP in the United States and Europe, as a result of combinations of antiretroviral therapy and PCP prophylaxis, might lessen the enthusiasm for continued study of this issue, brief consideration of a number of factors that warn of a future “perfect storm” suggests that continued study is important. First, most HIV-infected persons worldwide reside in sub-Saharan Africa, Southeast Asia, and Latin America, places where access to antiretroviral therapy and PCP prophylaxis are limited. Second, PCP is increasingly being recognized as an important cause of illness in these regions. In many of these regions, programs to use TMP-SMX as multiopportunistic infection prophylaxis are being implemented, and Pneumocystis that contains DHPS mutations can be expected. Next, the treatment options for PCP in these regions are often limited to TMP-SMX, since regimens such as pentamidine, clindamycin plus primaquine, trimetrexate, and atovaquone are unavailable. The existence of TMP-SMX–resistant Pneumocystis in these regions, combined with the general absence of invasive diagnostic procedures (e.g., bronchoscopy that might establish an earlier diagnosis of PCP when the outcome is better) and intensive care procedures (e.g., mechanical ventilation that might support patients until PCP treatment can be effective), stresses the importance of further study (40).
Dr. Huang is supported by the National Institutes of Health K23 HL072117.
Dr. Huang is an associate professor of medicine at the University of California San Francisco and an attending physician in the Department of Medicine at San Francisco General Hospital. He holds dual appointments in the Positive Health Program for HIV/AIDS and the Division of Pulmonary and Critical Care Medicine at San Francisco General Hospital. His clinical and research interests are focused on HIV-associated pulmonary diseases, especially Pneumocystis pneumonia.
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