Revisiting Species Distribution and Antifungal Susceptibility of Candida Bloodstream Isolates from Latin American Medical Centers

Abstract

The epidemiology of candidemia varies geographically, and there is still scarce data on the epidemiology of candidemia in Latin America (LA). After extensive revision of medical literature, we found reliable and robust information on the microbiological aspects of candidemia in patients from 11 out of 21 medical centers from LA countries and 1 out of 20 from Caribbean countries/territories. Based on 40 papers attending our search strategy, we noted that C. albicans remains the most common species causing candidemia in our region, followed by C. parapsilosis and C. tropicalis. In Argentina, Brazil, and Colombia, a trend towards an increase in frequency of C. glabrata candidemia was observed. Although resistance rates to fluconazole is under 3%, there was a slight increase in the resistance rates to C. albicans, C. parapsilosis and C. tropicalis isolates. Echinocandin resistance has been reported in a few surveys, but no single study confirmed the resistant phenotype reported by using molecular methods. We highlight the importance of conducting continuous surveillance studies to identify new trends in terms of species distribution of Candida and antifungal resistance related to episodes of candidemia in LA. This information is critical for helping clinicians to prevent and control Candida bloodstream infections in their medical centers.

1. Introduction

Fungi has been increasingly recognized as major agents of nosocomial infections in contemporary medicine, with emphasis on Candida spp., that accounts for the majority of invasive fungal infections associated in healthcare facilities. Indeed, besides being highly prevalent in Latin America countries, candidemia is associated with high morbidity and mortality rates, especially in critically ill patients [1,2,3,4,5,6,7].

The epidemiology of candidemia varies geographically, and, although C. albicans is still considered the most common cause of candidemia, there is a concern with the increasing rates of invasive infections due to Candida non-albicans (CNA) species in different parts of the world [7,8,9,10]. The reasons for the differences in species distribution and for the emergence of CNA species are not fully understood. However, there seems to be an association with a combination of variables related to host underlying conditions and medical interventions, including different practices of antifungal prophylaxis and resources available for prevention of health care associated infections [5,9,11,12,13,14,15,16,17].

Recognition of the importance of Candida infections has led to a significant increase in the use of antifungal agents in regiments of prophylaxis and empirical therapy, resulting in the emergence of resistant clinical isolates, particularly against triazoles and echinocandins [18,19]. In this scenario, the recent emergence of fluconazole resistance among isolates that are usually primarily sensitive to this drug, including C. parapsilosis and C. tropicalis strains, is worth mentioning [8,20,21,22,23,24]. Regarding to echinocandins, though resistance is still considered uncommon, occurrence of isolates with lower susceptibility to this therapeutic class has been increasingly reported, particularly among C. glabrata isolates [19,25,26,27].

The awareness of local epidemiology and antifungal susceptibility profile of Candida infections in different medical centers has major relevance in terms of guiding clinicians in optimizing their strategy for prevention and treatment of such fungal infections. This review attempts to provide a better understanding of the landscape of species distribution and antifungal resistance rates among Candida bloodstream isolates obtained from patients admitted in Latin American and Caribbean medical centers.

2. Methods

Our search strategy for the literature review was based on extensive revision of publications listed at PubMed, Scientific Electronic Library Online (SciELO), and MEDLINE bibliographic databases along the period between 1997 and 2016, irrespective of language and country of publication. Papers were retrieved using the following key words: candidemia, fungemia, Candida bloodstream infection, invasive candidiasis, Candida species distribution, antifungal susceptibility, and antifungal resistance. For each of these subjects, we also narrowed our search by adding the continent and country including the following: Central America, Latin America, South America, Caribbean, Argentina, Bolivia, Brazil, Chile, Colombia, Costa Rica, Cuba, Dominican Republic, Haiti, Honduras, Jamaica, Mexico, Panama, Peru, Puerto Rico, Uruguay, and Venezuela. Papers were included in our analysis only if their methodology and results matched the following criteria: (i) Candida isolates were identified at species level by a reliable and accurate phenotypic or molecular method; (ii) availability of data related to at least 50 Candida bloodstream isolates sequentially collected from different patients admitted in tertiary hospitals along the period of study; (iii) information regarding antifungal susceptibility of Candida spp. generated by The European Committee on Antimicrobial Susceptibility Testing (EUCAST) or Clinical Laboratory Standard Institute (CLSI) microbroth methods. Rates of resistance to triazoles and echinocandins reflect the breakpoints available at the time when the study was published. Papers addressing identification and susceptibility tests of worldwide collections of Candida isolates were considered only if isolates were obtained from patients with candidemia and data from Latin American or Caribbean countries were addressed separately. For antifungal susceptibility results, we only considered studies that tested at least 60% of all original collections of Candida strains originally selected for the study.

3. Results

We identified 40 studies that contained our inclusion criteria providing data of species distribution and antifungal susceptibility of Candida strains related to episodes of candidemia documented in Latin American and Caribbean medical centers.

In terms of geographic origin, 22 papers were from Brazil, 4 from Argentina, 4 from Colombia, 2 from Mexico, and 1 each representing the following countries: Costa Rica, Peru, Venezuela, and Puerto Rico (Caribbean region). Of note, Puerto Rico is an unincorporated territory of the United States of America (USA), located in the Caribbean. In addition to 36 studies reporting data of single countries, we also evaluated results provided by 4 multicenter studies that tested Candida spp. bloodstream isolates from multiple Latin American countries including Argentina, Brazil, Chile, Colombia, Costa Rica, Ecuador, Honduras, Mexico, Peru, Uruguay, and Venezuela. In this scenario, we identified papers characterizing the etiologic pattern and antifungal susceptibility of episodes of candidemia documented in only 11 out of 21 Latin American countries and 1 out of 20 Caribbean countries and territories. Taking together all data available, we were able to characterize the species distribution in more than 12,000 episodes of Candida bloodstream infections documented in 40 medical centers from our region (

Table 1. Species distribution of Candida bloodstream isolates from Latin American and Caribbean medical centers (1997–2016).

Country/Territory	Reference	Period	n e (No. of Centers)	Species Distribution (%)
				Ca a	Cp a	Ct a	Cgla a	Ck a	C. gui a	OCS b
Argentina	Rodero et al. (2005) [28] c	1999–2000	253 (36)	42.5	29.9	16.5	2.7	1.18	0.39	6.83
Argentina	Cordoba et al. (2011) [29] c	2007–2008	420 (47)	42.1	28.5	16.9	4.7	0.47	1.66	5.67
Argentina	Lopez Moral et al. (2012) [30] c	2005–2008	683 (16)	41.3	24.3	19.9	6.3	0.59	1.76	5.85
Argentina	Riera et al. (2014) [31]	2010–2012	158 (4)	41	20	12	10	1.5	3	12.5
Brazil	Colombo et al. (1999) [32]	1995–1996	145 (6)	37	25	24	4	1	2	7
Brazil	Costa et al. (2000) [33] c	1994–1996	84 (1)	51.2	17.8	11.9	2.3	1.19	9.5	6.11
Brazil	Colombo et al. (2003) [34]	1996–1998	200 (5)	41.5	20.5	24	4.5	1	2	6.5
Brazil	Goldani and Mario (2003) [35] c	1996–1999	101 (1)	32.6	23.7	26.7	8.9	1.9	0	6.2
Brazil	Antunes et al. (2004) [36]	2002–2003	120 (1)	48.3	25.8	13.3	3.3	1.7	1.6	6
Brazil	Aquino et al. (2005) [37]	1998–2004	131 (1)	45	24.4	15.3	6.9	4.6	0.76	3.04
Brazil	Colombo et al. (2006) [38]	2003–2004	712 (11)	40.9	20.5	20.9	4.9	1.1	2.4	9.3
Brazil	Medrano et al. (2006) [39]	2000–2002	50 (1)	28	36	16	4	0	12	4
Brazil	Colombo et al. (2007) [40]	2002–2003	282 (4)	38	23	17	3	1	6	12
Brazil	da Matta et al. (2007) [41]	1995–2003	1000 (4)	40	23.8	24.3	4.4	0.6	3	3.9
Brazil	Girao et al. (2008) [42]	1999–2006	108 (1)	40	18	34	1	3	1	3
Brazil	Franca et al. (2008) [43]	2001–2004	100 (1)	59	9	15	7	2	2	6
Brazil	Motta et al. (2010) [44]	2006	136 (1)	52.2	22.1	14.7	6.6	1.6	0.8	2
Brazil	Sampaio Camargo et al. 2010 [45]	1997–2007	151 (1)	44	22	15	9	6	0.66	3.34
Brazil	Bonfietti et al. (2012) [46]	1998–2006	100 (1)	44	37	13	5	1	0	0
Brazil	Hoffmann-Santos et al. (2013) [47]	2006–2011	130 (2)	34.6	38.4	18.4	5.3	0	1.5	1.8
Brazil	Moretti et al. (2013) [48]	2006–2010	313 (1)	44	14.4	21.7	11.2	3.5	1.3	3.9
Brazil	Colombo et al. (2013) [15]	2006–2007	300 (9)	34	26	24	7	3	2	4
Brazil	Santos et al. (2014) [49]	1995–2009	422 (1)	35.7	46.6	9.7	3.5	0.94	1.65	1.91
Brazil	Colombo et al. (2014) [2]	2003–2012	1392 (22)	42	19	20	9	1.14	0.86	8
Brazil	da Costa et al. (2014) [50]	2006–2011	108 (1)	28.7	24.1	30.5	8.3	1.8	0	6.6
Brazil	Doi et al. (2016) [51]	2007–2010	137 (16)	34.3	24.1	15.3	10.2	1.5	0.7	13.9
Colombia	Cortes et al. (2011) [52] c	2001–2007	1622 (27)	50.9	15.5	15.5	2	2.36	3.3	10.44
Colombia	Cortes et al. (2013) [53]	2004–2008	382 (7)	56	16	17.3	2.6	0.8	0	7.3
Colombia	Cortes et al. (2014) [54]	2008–2009	131 (7)	66.4	14.5	10.6	1.5	0	1.5	5.5
Colombia	Ortiz Ruiz et al. (2016) [55]	2008–2012	81 (3)	52	17	17	6	3	4	1
Costa Rica	Villalobos et al. (2016) [56]	2007–2011	210 (1)	38	42	10	7	NR f	NR	3
Mexico	Gonzalez et al. (2008) [57]	2004–2007	398 (5)	31.9	37.9	14.8	8	2.7	1.3	3.3
Mexico	Corzo-Leon et al. (2014) [58]	2008–2010	74 (2)	46	5	26	13.5	5	3	1.5
Peru	Bustamante et al. (2014) [59]	2009–2011	153 (1)	39.9	28.1	23.5	5.2	0.7	2	0.6
Puerto Rico	Conde-Rosa et al. (2010) [60]	2005–2006	85 (1)	28	49	17	4	1	0	1
Venezuela	Franco et al. (2008) [61]	2003–2005	154 (6)	18.8	26	39	7.8	2.6	0	5.8
Multic d	Pfaller et al. (2000) [62]	1997–1998	107 (7)	43	26.1	16.8	6.6	0.9	0	6.6
Multic	Pfaller et al. (2001) [63]	1997–1999	132 (9)	45	25	16	6	1	NR	7
Multic	Godoy et al. (2003) [64]	1999–2000	103 (5)	42	21.3	24.2	7.7	0	2.9	1.9
Multic	Nucci et al. (2013) [7]	2008–2010	672 (21)	37.6	26.5	17.6	6.3	2.7	6.5	2.8

^a Ca: C. albicans. Cp: C. parapsilosis (sensu lato). Ct: C. tropicalis. Cgla: C. glabrata. Ck: C. krusei. Cgui: C. guilliermondii (sensu lato); ^b Other Candida Species—species other than C. albicans. C. parapsilosis (sensu lato). C. tropicalis. C. glabrata. C. krusei. C. guilliermondii (sensu lato); ^c Fungemia collection. Percentage of species distribution was recalculated taking in account only Candida species as denominator; ^d Multicenter studies including different countries in Latin America; ^e Number of Candida isolates; and ^f NR: Not Reported.

, Figure 1, and Supplementary Material). Among all Candida spp. isolates analysed for species distribution, only 5460 isolates had their antifungal susceptibility profile performed in 17 studies (

Table 2. Azole resistance rates of C. albicans, C. parapsilosis (sensu lato) and C. tropicalis bloodstream isolates from Latin American medical centers (1997–2016).

Country	Reference; Number of Isolates	Method	Species	Fluconazole		Voriconazole
				SDD a	R b	SDD	R
Argentina	Rodero et al. (2006) [28];	CLSI c ×	Ca e	NR i	15.7% (1.8%)	NT j	NT
	n = 265	(EUCAST)	Cp f	NR	0% (0%)	NT	NT
			Ct g	NR	43% (5.4%)	NT	NT
Argentina	Cordoba et al. (2011) [29];	EUCAST d	Ca	NR	0%	NR	0.5%
	n = 420		Cp	NR	2.5%	NR	0.8%
			Ct	NR	4.2%	NR	4.2%
Brazil	Colombo et al. (2003) [34];	CLSI	Ca	1.2%	0%	NT	NT
	n = 200		Cp	0%	0%	NT	NT
			Ct	0%	0%	NT	NT
Brazil	Antunes et al. (2004) [36];	CLSI	Ca	0%	0%	NT	NT
	n = 120		Cp	0%	0%	NT	NT
			Ct	0%	0%	NT	NT
Brazil	Aquino et al. (2005) [37];	CLSI	Ca	0%	0%	NT	NT
	n = 131		Cp	0%	0%	NT	NT
			Ct	0%	0%	NT	NT
Brazil	Colombo et al. (2006) [38];	CLSI	Ca	0.3%	0.3%	0%	0.3%
	n = 712		Cp	0%	0%	0%	0%
			Ct	1.3%	0%	0%	0%
Brazil	Colombo et al. (2007) [40];	CLSI	Ca	0%	0%	NT	NT
	n = 282		Cp	0%	0%	NT	NT
			Ct	0%	0%	NT	NT
Brazil	da Matta et al. (2007) [41];	CLSI	Ca	0%	0%	0%	0%
	n = 1000		Cp	0%	0%	0%	0%
			Ct	0%	0%	0%	0%
Brazil	Bonfietti et al. (2012) [46];	EUCAST	Ca	0%	0%	0%	0%
	n = 100		Cp	6%	0%	0%	3%
			Ct	0%	0%	0%	0%
Brazil	Colombo et al. (2013) [15];	CLSI	Ca	0%	0%	0%	0%
	n = 300		Cp	1.3%	0%	0%	0%
			Ct	2.5%	0%	0%	0%
Brazil	Santos et al. (2014) [49];	CLSI	Ca	9.9%	0%	2.6%	0%
	n = 422		Cp	7%	0%	3.5%	0%
			Ct	19.5%	7.3%	12%	4.9%
Brazil	da Costa et al. (2014) [50];	EUCAST	Ca	NR	3.7%	NR	3.7%
	n = 108		Cp	NR	26.9%	NR	0%
			Ct	NR	3,2%	NR	3.2%
Mexico	Gonzalez et al. (2014) [57];	CLSI	Ca	0%	0.8%	0%	0.8
	n = 398		Cp	0%	0%	0%	0%
			Ct	0%	0%	0%	0%
Mexico	Corzo-Leon et al. (2014) [58];	CLSI	Ca	0%	0%	0%	0%
	n = 74		Cp	0%	0%	0%	0%
			Ct	0%	0%	0%	0%
Peru	Bustamante et al. (2014) [59];	CLSI	Ca	NR	NR	0%	5%
	n = 153		Cp	NR	2.3%	NR	NR
			Ct	NR	NR	NR	NR
Multicenter	Godoy et al. (2003) [64];	CLSI	Ca	0%	0%	NT	NT
studies h	n = 103		Cp	0%	0%	NT	NT
			Ct	0%	0%	NT	NT
Multicenter	Nucci et al. (2013) [7];	CLSI	Ca	0,4%	0%	0%	0%
studies	n = 672		Cp	1,1%	0%	0%	0%
			Ct	0%	0%	0%	0%

^a Susceptible in a dose-dependent manner; ^b Resistant to azoles; ^c Clinical Laboratory Standard Institute; ^d European Committee on Antimicrobial Susceptibility Testing; ^e C. albicans; ^f C. parapsilosis (sensu lato); ^g C. tropicalis; ^h Multicenter studies including different countries from Latin America; ⁱ NR: Not reported; ^j NT: Not tested.

).

C. albicans, C. parapsilosis (sensu lato), C. tropicalis, and C. glabrata were the most commonly found species causing candidemia in all countries. C. albicans was the main cause of candidemia in 32 out of 40 studies exhibiting prevalence rates ranging between 18.8% and 66%. The highest prevalence rate of C. albicans candidemia was reported by Cortes et al. (2014) in Colombia [54]. It is worth to mention that all 4 studies from Colombia had C. albicans prevalence rates higher than 50%. In contrast, less than 30% of prevalence rates of C. albicans strains were reported in Brazil by Medrano et al. (2006) and da Costa et al. (2014), by Conde-Rosa et al. (2010) in a single study reported in Puerto Rico, and by Franco et al. (2008) in Venezuela [39,50,60,61]. In these studies, C. tropicalis and/or C. parapsilosis were the most commonly found species causing candidemia.

C. parapsilosis (sensu lato) isolates ranged from 5% to 49% of all candidemic episodes. Indeed, C. parapsilosis was identified as the main agent of CNA species candidemia in 25 out of 40 studies, and in 6 of the studies it surpassed the prevalence rate of C. albicans.

C. tropicalis was the second most common CNA species isolated in our region exhibiting prevalence rates ranging between 9.7% and 39%. Of note, C. tropicalis was the main cause of CNA species candidemia in 13 out of 40 studies. Franco et al. (2008) and da Costa et al. (2014) reported that C. tropicalis surpassed C. albicans in their surveys of candidemia [50,61]. In 2 casuistics conducted by Cortes et al. (2011) and Ortiz Ruiz et al. (2016), C. parapsilosis (sensu lato) and C. tropicalis infected exactly the same percentage of patients [52,55].

Prevalence rates of C. glabrata presented a large variation among studies documented in different countries. In general, C. glabrata represented the third or fourth most common CNA species documented in Candida bloodstream infections, exhibiting prevalence rates ranging from 1% to 13.5%. The highest rate for this species was found by Corzo-Leon et al. (2014) in Mexico where C. glabrata was considered the second most common cause of CNA candidemia behind only C. tropicalis [58].

Prevalence rates of C. krusei strains ranged from 0 to 6% among all studies. C. guilliermondii (sensu lato) was isolated in 33 out 40 studies, being reported in almost all countries represented in this review. The prevalence of C. guilliemondii candidemia ranged from 0 to 12%. The highest prevalence rate of C. guilliermondii candidemia was found in Honduras, as reported by Nucci et al. (2013), along with the characterization of 672 episodes of candidemia carried out in Latin America [7].

All species other than C. albicans, C. parapsilosis (sensu lato), C. tropicalis, C. glabrata, C. krusei, and C. guilliermondii (sensu lato) were classified as other Candida species (OCSs). The highest rate of OCSs among the studies retrieved was observed by Doi et al. (2016) in Brazil with 13.9% of its collection [51]. Overall, the most common species documented, in at least 5 out of 40 studies, were C. rugosa, C. pelliculosa, C. lusitaniae, C. famata, C. lipolytica, and C. kefyr. The OCSs less frequently isolated were C. haemulonii, C. intermedia, C. sake, C. holmii, C. zeylanoides, C. utilis, C. viswanathii, C. dubliniensis, and C. novergensis.

Overall, we were able to identify historical trends in species distribution of Candida spp. only related to prevalence of C. glabrata. In this regard, as illustrated on Table 1, only 1 out of 8 Brazilian studies published between 1997 and 2006 presented prevalence rates of C. glabrata candidemia ≥7%. Otherwise, 7 out of 14 studies published between 2007 and 2016 exhibited prevalence rates ≥7%. Similarly, in Argentina there was a substantially increment of C. glabrata rates moving from a rate of 2.7% in the first study reported in 2005 to 10% in a recent casuistic involving 158 episodes of candidemia reported by Riera et al. (2014) [31]. In Colombia, prevalence rates of C. glabrata in candidemia remained lower than 3% along the first 3 studies, as illustrated on Figure 1, moving up to 6% in a recent study involving 81 episodes of fungemia.

It is seems that there was a slight increase in the prevalence rate of C. krusei candidemia in Brazil. Indeed, 7 out of 8 studies from Brazil exhibited prevalence rates of C. krusei ≤ 2% between 1997 and 2006 [32,33,35,36,38,39,64]. In contrast, 5 out of 14 studies published between 2007 and 2016 exhibited isolation rates ≥2% for this particular species [15,42,43,45,48]. Prevalence rates of C. krusei candidemia remained stable along different studies reported in Argentina and Colombia (see Table 1).

Temporal Trends of Antifungal Resistance to Azoles and Echinocandins

An overall review of the 40 studies retrieved for Candida species distribution analysis, only 17 of them presented reliable information on the antifungal susceptibility tests of strains using broth microdilution methods standardized by CLSI and EUCAST. In order to check for trends in terms of rising antifungal resistance along the study period, we compared data from 7 studies published between 1997 and 2006 to data generated from 10 studies published between 2007 and 2016 (Table 2).

Ten out of the 17 studies providing data on Candida antifungal resistance were performed in Brazilian medical centers, 2 were from Argentina, 2 from Mexico, and 1 from Peru. We included an analysis of data generated by two multicenter studies that provided additional information from Argentina, Brazil, Chile, Colombia, Ecuador, Honduras, Peru, and Venezuela.

Reviewing the antifungal drugs that were evaluated along the 17 studies, we found that only fluconazole was tested in all them, followed by amphotericin B in 15 studies. Other drugs frequently tested included voriconazole (11 studies), caspofungin (5 studies), and anidulafungin (4 studies). Data on micafungin was only reported in one study.

It is important to mention that no single author from the Latin American surveys reporting rates of antifungal resistance of Candida bloodstream isolates, either to triazoles or echinocandins, attempted to confirm their in vitro profile by checking the expression of molecular mechanisms of antifungal resistance.

(i)

Trends in resistance to fluconazole and voriconazole among C. albicans, C. tropicalis, and C. parapsilosis isolates.

Resistance to azoles among isolates of C. albicans, C. tropicalis, and C. parapsilosis remained relatively unchanged over time. Except for one single study conducted by Rodero et al. (2005) in Argentina, all studies carried out prior to 2006 showed that less than 1% of isolates exhibited a non-susceptible (susceptible in a dose dependent manner [SDD] or resistant) phenotype to fluconazole and voriconazole. Regarding the Argentinean casuistic, the authors reported fluconazole resistance rates of 15.7% and 1.8% for C. albicans, and 43% and 5.4% for C. tropicalis, by using CLSI and EUCAST, respectively [28].

After 2007, a slight increase in the percentage of resistance to fluconazole was noted. Overall, resistance rates to fluconazole increased from 0.4% to 1.2% among C. albicans, from 0.5% to 2.3% among isolates of C. tropicalis, and from 0 to 2.6% for C. parapsilosis [7,15,29,46,49,50,57,59]. For voriconazole, resistance rates remained around 1%.

(ii)

Trends in resistance to echinocandins among Candida spp.

Only 7 out of 17 studies, all published after 2007, have provided data on antifungal susceptibility of at least one of the 3 echinocandins available for clinical use in Latin America. Of note, echinocandin resistance was reported in only 3 out of 7 mentioned studies. In Brazil, Santos et al. (2014) reported that 3 out of 15 (20%) of C. glabrata isolates were non-susceptible to caspofungin [49]. Similar data were observed by Bustamante et al. (2014) in Peru where 1 out of 8 (12.5%) of C. glabrata strains was resistant to anidulanfungin [59]. The only study reporting in vitro echinocandin resistance against species other than C. glabrata was conducted by Cordoba et al. (2011) in Argentina where they found 26 out of 120 (21.6%) of C. parapsilosis isolates resistant to anidulafungin by using the EUCAST microdilution method [29].

4. Discussion

Candidemia remains a significant public health problem worldwide [1,2,3,4,5,6,7]. In Latin America, the incidence rates range from 0.74 to 6.0 per 1000 hospital admissions [30,38,45,48,56,58]. Despite all advances related to the development of new diagnostic and therapeutic tools for fungal infections, crude mortality rates of candidemia remain high in Latin American medical centers, ranging from 30 to 76% [28,42,44,51,55,56,58,60].

As expected, C. albicans remains the most common species causing candidemia in our region, followed by C. parapsilosis and C. tropicalis [65,66]. Otherwise, prevalence rates of C. glabrata were highly variable within different studies and different countries. The same variation observed among several countries was noted in one recent global trend review of Candida species distribution, where prevalence rates of C. glabrata in candidemic patients in European medical centers ranged between 8% (Spain) and 20% (Denmark) [10]. In Brazil, Argentina and Colombia, we noted a trend towards an increase in C. glabrata frequency [28,31,41,48] along the period of study. This increase has an important clinical impact, as C. glabrata shows a diminished susceptibility to azoles and, eventually, candins [27]. Although the explanation for this shift is not completely understood, it seems to be a consequence of the increased exposure to fluconazole, as previously demonstrated by several authors [5,13].

C. krusei and C. guilliermondii (sensu lato) frequencies have not demonstrated substantial changes in their frequency, but both species were found in most studies from different countries. In fact, C. krusei was found in 36 out of 40 articles, while C. guilliermondii (sensu lato) was found in 33. Of note, in the single multicenter study conducted by Nucci et al. (2013) in 7 countries, C. guilliermondii ranged from 1.6% to 20% [7]. Due to their reduced susceptibility to fluconazole, both C. krusei and C. guilliermondii may have a relevant clinical impact in terms of defining strategy for empirical therapy of risk patients [67,68].

One limitation found in all studies reviewed is that only phenotypic methods were used to identify Candida species involved in the episodes of candidemia. Consequently, accurate identification of cryptic species of Candida could not be provided. In addition, we may not exclude the possibility that the OCSs reported by the authors, including C. rugosa, C. pelliculosa, C. lusitaniae, C. famata, C. lipolytica, and C. kefyr, were misidentified by inaccurate phenotypic methods used by the routine laboratories. There is a consensus that MALDI-TOF and sequencing of the Internal Transcribed Spacer (ITS) region of ribosomal DNA are both considered to be far more accurate and reliable for providing identification of cryptic and rare species of Candida than conventional methods [69,70,71].

In this regard, despite the fact that C. auris strains have not been detected as OCSs causing infection along the 40 mentioned surveys of candidemia performed in our region, two recent reports documented outbreaks of C. auris candidemia in medical centers from Venezuela and Colombia [72,73]. This microorganism has been recognized as a multidrug-resistant yeast pathogen since all C. auris strains are fully resistant to fluconazole and part of them may be either resistant to candins and/or amphotericin B. We may not exclude the possibility that the real prevalence of this emerging multidrug-resistant yeast pathogen is underestimated in our region since it has been misidentified in routine laboratories as C. famata and C. haemulonii, among others [74].

Fluconazole resistance has been increasingly noted in Candida spp., not only with C. glabrata but also among strains initially described as primarily sensitive to azoles such as C. parapsilosis and C. tropicalis [8,10,20,21,22,24,75,76,77]. In the review presented, we decided not to focus our analysis on fluconazole resistance against C. glabrata strains since fluconazole is not considered a safe alternative anymore for treating candidemic patients infected by this pathogen [67,68].

Several studies have reported variations in fluconazole resistance rates among C. parapsilosis and C. tropicalis isolates. Indeed, resistance rates among C. parapsilosis isolates ranged from 3.4% to 7.5% in USA and from 0 to 6% in Europe [8,20,21,22,75,76,77,78]. For C. tropicalis, resistance rates ranged from 2.4% to 11.6% in USA and from 1.7% to 22% in Europe [8,20,21,22,75,76,77,78]. In Latin America, we have noted a slight increase in C. albicans, C. parapsilosis, and C. tropicalis isolates exhibiting a non-susceptible profile to fluconazole along our study period. Indeed, resistance rates to fluconazole increased from 0.4% to 1.2% among C. albicans isolates; from 0.5% to 2.3% among isolates of C. tropicalis and from 0 to 2.6% for C. parapsilosis strains. Of note, though still considered rare, a recent publication from Brazil described an outbreak of C. parapsilosis (sensu stricto) candidemia involving 23 intensive care unit (ICU) patients from a single institution [24]. Resistance to fluconazole in C. parapsilosis strains in this particular report was confirmed by the presence of ERG11 mutations and overexpression of efflux pumps by the mentioned strains [79].

Resistance to echinocandins has been described as an uncommon phenomenon among C. albicans, C. parapsilosis, C. tropicalis, and C. krusei isolates [80]. However, it has become increasingly common among C. glabrata strains from patients admitted in US and European hospitals [27,80,81,82]. In Latin America, apparently, echinocandin resistance remains rare. It is important to mention that echinocandins are rarely used for the treatment of candidemic patients in Latin America in spite of the drug’s availability in the early 2000s.

According to Nucci et al. (2013), only 40 (5.9%) out of 672 patients with candidemia documented between 2008 and 2010 were initially treated with echinocandins [7]. Another aspect to consider is that antifungal resistance in Latin America may be underestimated since most routine laboratories do not perform antifungal susceptibility tests.

In our analysis, only 3 out of 40 studies documented any rate of echinocandin resistance with Candida sp. bloodstream isolates. Santos et al. (2014) and Bustamante et al. (2014) reported resistance rates of 20% and 12.5% to echinocandins among C. glabrata isolates, respectively [49,59]. Cordoba et al. (2011) reported that 21.6% of C. parapsilosis isolates were resistant to anidulafungin [29]. However, the high rates of resistance reported by these papers should be interpreted very carefully since they have not confirmed the echinocandin resistance phenotype by checking the presence of fks mutations in all isolates exhibiting high values of minimum inhibitory concentration (MIC) for echinocandins.

Currently, only two reports from medical centers in Latin America have demonstrated microbiological and molecular echinocandin resistance against Candida bloodstream isolates. Bizerra et al. (2014), using sequencing methodology for the study of FKS genes and quantification of glucan synthesis, reported the occurrence of a mutation associated with the resistance phenotype against echinocandins in C. glabrata isolated from a single cancer patient with candidemia exposed to antifungal prophylaxis with micafungin [25]. Finally, Forastiero et al. (2015) reported a rapid development of resistance in C. krusei isolates recovered from a patient under caspofungin treatment. Clinical resistance was associated with increased echinocandin MICs and was ultimately related to new mutations of the target enzyme (fks1) [83].

5. Conclusions

In conclusion, there has been a changing epidemiology of Candida bloodstream infection over the past years in Latin America. Although C. albicans remains the predominant cause of candidemia, a shift has been reported in the epidemiology as some CNA species have emerged as the cause of candidemia, and they can exhibit resistance to fluconazole and echinocandins. Several medical centers have reported episodes of candidemia due to C. tropicalis and C. parapsilosis isolates resistant to fluconazole. Echinocandin resistance confirmed by molecular studies has been reported in only two episodes of candidemia reported in patients assisted at medical centers from Latin America, and appears to be rare in our region. Continuous multicenter surveillance studies of candidemia in Latin America are necessary to detect any regional and historical trends, in terms of Candida species distribution and emergence of antifungal resistance, early. This information is critical to clinicians in preventing and controlling Candida bloodstream infections in our medical centers.