Research Article

Many Globally Isolated AD Hybrid Strains of Cryptococcus neoformans Originated in Africa

  • Anastasia P Litvintseva mail,

    To whom correspondence should be addressed. E-mail:

    Affiliation: Department of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, North Carolina, United States of America

  • Xiaorong Lin,

    Affiliation: Department of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, North Carolina, United States of America

  • Irka Templeton,

    Affiliation: Department of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, North Carolina, United States of America

  • Joseph Heitman,

    Affiliation: Department of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, North Carolina, United States of America

  • Thomas G Mitchell

    Affiliation: Department of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, North Carolina, United States of America

  • Published: August 17, 2007
  • DOI: 10.1371/journal.ppat.0030114


Interspecific and intervarietal hybridization may contribute to the biological diversity of fungal populations. Cryptococcus neoformans is a pathogenic yeast and the most common fungal cause of meningitis in patients with AIDS. Most patients are infected with either of the two varieties of C. neoformans, designated as serotype A (C. neoformans var. grubii) or serotype D (C. neoformans var. neoformans). In addition, serotype AD strains, which are hybrids of these two varieties, are commonly isolated from clinical and environmental samples. While most isolates of serotype A and serotype D are haploid, AD strains are diploid or aneuploid, and contain two sets of chromosomes and two mating type alleles, MATa and MATα, one from each of the serotypes. The global population of serotype A is dominated by isolates with the MATα mating type (Aα); however, about half of the globally analyzed AD strains possess the extremely rare serotype A MATa allele (Aa). We previously described an unusual population of serotype A in Botswana, in which 25% of the strains contain the rare MATa allele. Here we utilized two methods, phylogenetic analysis of three genes and genotyping by scoring amplified fragment length polymorphisms, and discovered that AD hybrid strains possessing the rare serotype A MATa allele (genotype AaDα) cluster with isolates of serotype A from Botswana, whereas AD hybrids that possess the MATα serotype A allele (AαDa and AαDα) cluster with cosmopolitan isolates of serotype A. We also determined that AD hybrid strains are more resistant to UV irradiation than haploid serotype A strains from Botswana. These findings support two hypotheses: (i) AaDα strains originated in sub-Saharan Africa from a cross between strains of serotypes A and D; and (ii) this fusion produced hybrid strains with increased fitness, enabling the Botswanan serotype A MATa genome, which is otherwise geographically restricted, to survive, emigrate, and propagate throughout the world.

Author Summary

Hybridization between individuals of different species or varieties is common among fungi. However, the impact of hybridization on the evolution of pathogenic fungi is unresolved. Several hybrids of phytopathogenic fungi exhibit expanded host ranges. To our knowledge, this report is the first description of increased hybrid fitness (hybrid vigor) in a human pathogen, Cryptococcus neoformans, the most prevalent cause of fungal meningitis. We demonstrate that diploid hybrid strains are common among both environmental and clinical isolates of two varieties, represented by serotypes A and D. We determined that many globally isolated AD hybrid strains originated in sub-Saharan Africa and have increased resistance to ultraviolet radiation. We hypothesize that hybrid strains have increased fitness, which enabled them to emigrate from Africa and spread globally.


The impact of hybridization between fungal species and varieties on their evolution is unresolved. Hybridization may be considered an evolutionary disadvantage because some interspecies hybrids have reduced fitness [1,2]. Alternatively, natural hybridization may be beneficial because it can generate new evolutionary lineages that are able to occupy novel ecological niches [25]. In recent years, several examples of epidemiologically successful interspecific hybrids that were able to colonize new environments and infect new hosts have been described among fungal plant pathogens [57] and oomycetes [4]. These hybrids illustrate the effect of natural hybridization on the production of biological diversity in fungal populations.

C. neoformans is an opportunistic human pathogen that is acquired exogenously and readily isolated from the environment worldwide [8]. Based on serological differences in capsular epitopes and molecular phylogenetic evidence, two varieties are recognized: C. neoformans var. grubii, which encompasses isolates of serotype A, and C. neoformans var. neoformans, which includes isolates of serotype D [810]. These varieties represent monophyletic lineages that diverged approximately 18 million years ago [11,12], and according to the phylogenetic species concept, they may reflect cryptic species [13]. More than 90% of clinical isolates from patients with cryptococcosis are strains of serotype A. Strains of serotype D are also found globally, but they are more prevalent in Europe [14]. The clinical manifestations of human infections with serotype A or D appear to be similar, but experimental infections suggest that strains of serotype A are more virulent than strains of serotype D [8,15].

AD strains are hybrids of the two varieties. Whereas most isolates of serotypes A and D are haploid, AD strains are diploid or aneuploid, contain two sets of chromosomes, and possess two mating type alleles, one from each of the two serotype A and D haploid genomes [1618]. Recent reports suggest that hybrid AD strains may be more common in clinical samples then previously appreciated. For example, a prospective survey of cryptococcosis in Europe from 1997 to 2001 found that up to 30% of all isolates of C. neoformans from patients in Europe were AD hybrids [14]. Strains of both serotype A and serotype D, as well as AD hybrids, are found in the environment, where they are primarily associated with avian feces. Our recent analysis of environmental and clinical populations of C. neoformans in North America revealed that approximately 7.5% of strains isolated from the environment are AD hybrids [19].

C. neoformans has a bipolar mating system with two alternative mating type alleles, MATa or MATα. When sexual reproduction is induced in the laboratory, haploid MATa and MATα strains of serotype A or serotype D are capable of plasmogamy, karyogamy, and meiosis, during which they produce dikaryotic hyphae, basidia, and chains of haploid basidiospores. Although most naturally occurring AD hybrid strains are incapable of mating with strains of the opposite mating type, some AD hybrid strains are self-fertile. That is, when stimulated by growth on mating medium in the absence of a mating partner, they produce hyphae, basidia, and basidiospores [16,20]. Most of the basidiospores produced by these self-fertile AD hybrid strains fail to germinate, which suggests that meiosis is impaired in these hybrids. However, approximately 5% of these spores germinate to produce viable diploid, aneuploid, and rarely, haploid cells [16,20,21]. In addition, postzygotic reproductive isolation of serotype A and serotype D is supported by phylogenetic analyses of multiple gene genealogies, which is consistent with the monophyletic origins of both serotypes [11,12,22], and by a comparative genomics analysis of representative strains of serotype A and serotype D, which confirmed that recombination is rare between these serotypes [23].

Clinical and environmental populations of both serotype A and serotype D are dominated by isolates with the MATα mating type. Isolates of serotype D with the rare MATa mating type have been known for some time [8], and recently, a few strains of serotype A with the MATa allele have been isolated from Tanzania [24,25], Italy [26], Hungary [27], and Botswana [28]. However, with the exception of the unique subpopulation of serotype A in Botswana (designated VNB strains), in which 25% of the isolates possessed the MATa allele, the prevalence of the MATa allele among global isolates of serotype A is less than 0.1% [22].

Although the MATa allele is extremely rare among global isolates of serotype A, the MATa serotype A allele is common among AD hybrids. Several reports indicate that from 20% to 80% of AD hybrids contain the AaDα genotype [1619,29]. At least two hypotheses have been proposed to explain the rarity of serotype A MATa allele among strains of serotype A but its high prevalence in serotype AD hybrids [16,19,24]: (i) nearly all serotype A isolates with the MATa allele are extinct, and AD hybrids represent historic evidence that strains with the MATa allele were once more abundant; and (ii) isolates of serotype A with the MATa allele are extant, but they are geographically isolated, exist in a different natural reservoir, and/or are nonpathogenic; consequently, they are rarely recovered from environmental samples or clinical specimens.

Our recent discovery of the VNB subpopulation of serotype A in Botswana, which includes a significant number of isolates with the MATa allele [22,28], invokes an alternative hypothesis about the origin of AaDα hybrids. These hybrids may have originated from sexual encounters between one or more strains of serotype D and one or more VNB strains of serotype A with the MATa allele. The progeny of this union may have enjoyed increased fitness compared to the parental strains, enabling them to expand clonally and disseminate beyond Africa. To test this hypothesis, we investigated whether serotype A MATa alleles in non-Botswanan AD hybrids could have originated from the VNB subpopulation of serotype A, and whether hybrid strains are fitter than strains of serotype A or serotype D.


Half of AD Hybrid Strains Isolated from Three Continents Possess the Rare Serotype A MATa Allele

To ascertain the distribution of the mating type alleles in the AD strains, serotype-specific PCR primers were used to amplify fragments of STE20 gene situated within the MAT locus [25]. Five strains, isolated from China, Italy, Kuwait, and the United States of America, generated characteristic products with the PCR primers specific to the serotype A STE20 MATα allele (Figure 1C) and serotype D STE20 MATa allele (Figure 1A, lanes 2, 5–7, and 10), and therefore were identified as AαDa strains (Table 1). Conversely, six strains isolated from China, Italy, and the US produced characteristic amplicons with the PCR primers specific to the serotype A STE20 MATa allele (Figure 1B). A pair of PCR primers that were mating-type-specific but non-serotype-specific amplified the STE20 MATα gene from all of the strains (Figure 1D). The DNA sequences of these fragments were compared with the available sequences of STE20 genes for both serotype A [30]. As expected, PCR products obtained from four strains from the US (CDC228, CDC304, MMRL1365, and nc34–21), one strain from China (ZG290), and one strain from Italy (it752) were identical to the reference serotype D STE20α sequence, while they exhibited 5% nucleotide polymorphisms with the reference serotype A STE20α sequence (Table 2). Thus, they were identified as AaDα strains. An environmental isolate from the US (nc5–19, Figure 1, lane 4) contained two copies of the STE20α allele, one from serotype D and the other from serotype A, and therefore had the unusual AαDα genotype, which is consistent with our previous observations ([19] and X. Lin, A. Litvintseva, K. Nielsen, S. Patel, A. Floyd, et al., unpublished data).


Figure 1. PCR Amplification of Portions of the STE20 Gene from the AD Hybrid Strains Using Mating Type– and Serotype-Specific Primers

(A) PCR primers specific to MATa serotype D allele (STE20Da); (B) PCR primers specific to MATa serotype A allele (STE20Aa); (C) PCR primers specific to MATα serotype A allele (STE20Aα); (D) PCR primers specific to MATα serotype A/D allele (STE20A/Dα). Lanes 1–12 represent the following strains (from left to right): CDC228, it755, ZG290, nc5–19, it756, it744, KW5, it752, CDC304, ZG287, nc34–21, and MMRL1365.


Table 1.

Strains of Cryptococcus neoformans Used in This Study


Table 2.

DNA Identity between Portions of STE20 of Different Strains


AFLP Genotypes of AaDα and AαDa Strains Are Different

To examine the genetic relationships among the 12 AD strains, amplified fragment length polymorphism (AFLP) genotyping was conducted with two independent primer pairs [28]. Eighteen polymorphic bands were generated, which differentiated six unique AFLP genotypes. As shown in Figure 2, AFLP band patterns of the AaDα strains are more similar to each other than to the AαDa strains: at least five distinct AFLP bands are characteristic of either one of the groups. Two different genotypes were observed among AaDα strains, and three genotypes were identified among AαDa strains. The AFLP banding pattern of the unusual AαDα genotype (strain nc5–19) was similar to that of the AαDa strains.


Figure 2. Computer-Generated AFLP Band Patterns of AD Hybrid Strains

Lanes 1–6 represent AaDα strains CDC228, CDC304, it752, nc34–21, and MMRL1365, respectively. Lanes 7–12 represent AαDa strains ZG287, KW5, it744, it755, it756, and nc5–19, respectively. Lane 12 represents the unusual nc5–19 isolate that carries both serotype A and serotype D MATα alleles (AαDα). Bands that are polymorphic between Aa and Aα groups are indicated with long arrows, and bands that are polymorphic among the individual strains are denoted with short arrows. AFLP bands that were consistent between independent DNA preparations and analyses (see Materials and Methods) are labeled with the asterisks.


MLST Analyses Reveal That AaDα Isolates Are Related to VNB Strains from Botswana

Previously, we developed a 12-gene multi locus sequence typing (MLST) genotyping system that allows unambiguous genotyping of strains of serotype A; however, this system is impractical for the AD hybrid population, because AD hybrids contain two copies of each loci, both of which are PCR-amplified using our MLST primers [22]. Consequently, we developed new PCR primers that selectively amplified serotype A alleles of three genes, CAP10, URE1, and GPD1, and generated amplicons of 410, 810, and 220 base pairs, respectively. We used these primer pairs to amplify DNA from the 12 AD hybrids and a global sample of 45 strains of serotype A, which represent unique genotypes in a previously described sample of 1,057 global isolates of serotype A (Table 1, [22]). DNA sequences of these genes were determined and subjected to phylogenetic analyses (Figure 3). For the CAP10 locus, 308 nucleotides were alignable, and five were phylogenetically informative; for the URE1 locus, 605 nucleotides could be aligned, and seven were phylogenetically informative; and for the GPD1 locus, 123 nucleotides were aligned, and three were phylogenetically informative.


Figure 3. Bayesian Consensus Tree for 12 AD Hybrid Strains and 45 Representative Strains of Serotype A Based on the Combined Data for the Three Loci

The tree is rooted with the sequences from the JEC21 strain of serotype D, and branch lengths leading to the outgroup are shortened to fit the figure. Thickened lines denote clades supported by Bayesian posterior probabilities ≥95%. VNI, VNII, and VNB refer to the subgroups (molecular types) identified within serotype A [22]. AaDα hybrid isolates are shown in blue, AαDa hybrid isolates are shown in green, and isolates from Botswana are shown in red. Strains of serotype A that possess MATa allele are marked with arrowheads.


Bayesian consensus trees were constructed for CAP10, GPD1, and URE1 (unpublished data), as well as the combined data for all three loci (Figure 3), and rooted with JEC21 strain of serotype D. Gene genealogies of all three loci and the combined genealogy were congruent, and the phylograms recognized the three major subpopulations of serotype A: VNI, VNII, and VNB [22]. The VNI group includes the majority of global isolates of serotype A, as well as three previously identified strains of serotype A with the MATa mating type, 125.91 [25], IUM 96-28-28 [26], and bt130 [28]. The VNII group has a small number of strains, and all have the MATα allele. The VNB group contains most of the known isolates of serotype A with the MATa allele [22]. DNA sequences of the CAP10, GPD1, and URE1 genes were identical among the six AaDα strains. The DNA sequences of these genes were also identical among six AD strains that possess the MATα serotype A allele, AαDa and AαDα. In all of these phylograms, AαDa and AαDα strains cluster with the VNI group, whereas the AaDα strains cluster with the VNB group that contains most of the serotype A MATa isolates (Figure 3).

We have not analyzed the origin of the serotype D counterpart in these AD hybrids because an MLST genotyping scheme for serotype D is not yet available. In addition, serotype D isolates are rare in the clinical samples and in the collection, which further complicates this analysis.

Natural and Laboratory AaDα Hybrids Are More Resistant to UV Irradiation Compared to Serotype A and Serotype D Haploid Strains

Previous analyses of AFLP and MLST genotypes of numerous strains of serotype A showed that the VNB subpopulation is geographically confined to Botswana [22]. Yet, we have shown here that AaDα hybrid strains with the VNB genome are distributed globally. One possible explanation for this apparent paradox is that hybridization produces hybrid strains with increased fitness that are better able to tolerate stress and/or propagate in the environment. Most strains of C. neoformans are highly sensitive to direct sunlight and temperatures above 38 °C, and both conditions exist in much of Botswana. To test the hypothesis of hybrid vigor associated with the AD hybrid genome, we compared the effects of elevated temperature and exposure to UV irradiation on the growth of haploid VNB strains and AD hybrids.

To compare fitness among strains of serotypes A, D, and AD hybrids with the same genetic background, AD hybrids were constructed in the laboratory by fusing ura5 mutants of bt65 and bt88 strains of serotype A from Botswana, and with an ade2 mutant of JEC21 strain of serotype D. Spontaneous ura5 mutants of bt65 and bt88 were obtained by selection on 5-fluoroorotic acid medium, which inhibits strains with the functional URA5 gene [31,32]. These ura5 mutants were coincubated with the ade2 mutant of JEC21 [33] on V8 medium (X. Lin, A. Litvintseva, K. Nielsen, S. Patel, A. Floyd, et al., unpublished data). Three prototrophic hybrid strains, designated XL1595, XL1596, and XL1597, were obtained and confirmed to be diploid by fluorescence-activated cell sorting (FACS) analysis.

Figure 4 illustrates that VNB isolates of serotype A are more sensitive to UV irradiation than laboratory-generated AD hybrids, naturally occurring AD hybrids, or control haploid strains of serotype A (H99) and serotype D (JEC21). UV irradiation for 24–30 seconds almost completely inhibited the growth of VNB strains and dramatically impaired growth of haploid control strains of serotype A (H99) and serotype D (JEC21); however, a significant number of AD hybrid cells survived this treatment (Figure 4A). The differences in survival between AD hybrids and haploid strains of serotypes A and D were statistically significant (p < 0.01, Figure 4B).


Figure 4. Natural and Laboratory AaDα Hybrids Are More Resistant to UV Irradiation Compared to Serotype A and Serotype D Haploid Strains

(A) VNB strains are more sensitive to UV irradiation than isolates of serotype D, VNI strain of serotype A, and AD hybrid strains. Cells were grown overnight in liquid culture under the melanin-inducing conditions, and 10-fold serial dilutions of log-phase yeast cells of VNB strains, AD hybrid strains, and control serotype A and serotype D strains were plated in triplicates on YPD medium; plates were UV irradiated (~48 mJ/cm2) for 24 (second panel) or 30 seconds (third panel). To evaluate the amount of melanin produced, strains were spotted on the plates containing low-glucose L-DOPA medium (last panel).

(B) Quantitative assessment of UV resistance for each strain. The highest dilutions that yielded colonies after treatment with UV were identified, and the number of individual colonies was determined within each spot corresponding to the highest dilution that yielded viable colonies. From this number, the total number of CFU that survived the treatment was determined and plotted. The experiment was performed in triplicate, and error bars represent standard error of the mean based on three replicates. Black bars represent cells irradiated for 24 seconds and grey bars represent cells irradiated for 30 seconds. Some AD hybrids are aneuploid (>1n but <2n).


Several lines of evidence suggest that C. neoformans is melanized in the natural environment [34,35], and the amount of melanin is known to affect susceptibility of the fungus to environmental stress [3638]. Therefore, UV irradiation experiments were performed under melanin-inducing conditions. Figure 4A shows that resistance to UV irradiation is not dependent upon the amount of melanin produced by each strain. Although most AD hybrids produced less melanin than haploid strains bt65, bt109, and H99 (Figure 4A, right panel), they were significantly more resistant to UV irradiation (Figure 4A, middle panels). Furthermore, the only heavily melanized hybrid, CDC228, was highly susceptible to UV radiation (Figure 4A, lower right panel).

Recently, we demonstrated that laboratory-generated hybrids with the AαDα genotype are more resistant to elavated temperature than either haploid parent strain (X. Lin, A. Litvintseva, K. Nielsen, S. Patel, A. Floyd, et al., unpublished data). Here, we compared the growth of AaDα hybrids at 40 °C. All of the hybrid strains tested, including laboratory-constructed (XL1595, XL1596, XL1597) and wild-type (ZG290 and nc34–21) hybrid strains, were capable of growing at 40 °C (unpublished data). Two of the haploid strains, JEC21 and bt65, were severely inhibited at 40 °C, whereas strain bt88 was not affected and survived well at 40 °C (unpublished data), which indicates that growth at high temperature can vary among VNB strains. All strains grew equally well on culture medium that contained pigeon excreta [35] as the sole source of carbon and nitrogen (unpublished data).


The high prevalence of the MATa serotype A allele among the AD hybrid strains has been puzzling because this allele is uncommon in the global population of serotype A. To investigate the origin of these strains, we designed serotype A–specific PCR primers that amplify three genomic regions situated on three different chromosomes of C. neoformans (CAP10, GPD1, and URE1) and constructed gene genealogies. These gene genealogies were congruent and revealed that both AαDa and AαDα hybrid strains cluster with isolates of the VNI group of serotype A, which is dominated by isolates with the MATα mating type. In contrast, AaDα strains cluster with the VNB group from Botswana, which contains a significant proportion of strains with the MATa allele [19].

Our results confirm data presented by Xu et al. [39], who used LAC1 and URA5 gene sequences to investigate phylogenetic relationships among serotypes A, D, and AD. Their LAC1 gene phylogeny revealed that AD hybrids are separated into two clusters: one included AD strains possessing the MATa serotype A allele, whereas the other included strains of serotype A and AD hybrids possessing the MATα serotype A allele. Their URA5 phylogram confirmed these clusters and also provided evidence of recombination between them, which is consistent with our observations [22,28].

The unusual clinical sample of serotype A isolates from Botswana consists of two genetically isolated subpopulations, VNI-Botswana and VNB [28]. Both groups are genetically unique and characterized by unusually high genotypic diversity. In addition, the VNB group contains an unprecedented proportion of fertile isolates with the MATa mating type and exhibits phylogenetic and population genetic evidence of recombination [22,28]. Here, we demonstrate that DNA sequences of the CAP10, GPD1, and URE1 genes in a global collection of AaDα hybrid strains are identical to those of two strains from Botswana, bt65 and bt88 (Figure 3, Table 1), which possess the MATa mating type and are fertile in the laboratory [28]. Therefore, it is likely that these, or related Botswanan strains, represent one of the progenitors of the many existing AaDα hybrids.

DNA sequences of the CAP10, GPD1, and URE1 genes were identical among the AD strains with the MATa serotype A allele (AaDα), as well as among the six AD strains that possess the MATα serotype A allele (AαDa and AαDα), which may indicate that the AD hybrids analyzed here are clonal descendents of only three ancestral strains with the AaDα, AαDa, and AαDα mating types. However, it is also possible that the loci we used here are insufficiently polymorphic to differentiate among these related strains. For example, we previously analyzed 12 MLST loci in over 100 global isolates of serotype A and demonstrated that two possible parental strains, bt65 and bt88, have closely related, but nevertheless distinct, genotypes. Similarly, this analysis of three MLST loci did not reveal the phylogenetic structure among the VNI isolates that we previously observed using 12 MLST loci and a larger sample of serotype A strains [22]. AaDα and AαDa strains are products of hybridization between isolates of opposite mating types (MATa and MATα), whereas AαDα is an apparent product of mating between isolates of the same mating type, which was recently described in C. neoformans ([40] and X. Lin, A. Litvintseva, K. Nielsen, S. Patel, A. Floyd, et al., unpublished data).

Genetic diversity among the isolates was also estimated by using AFLP, and the phylogenetic analyses based on these data demonstrated that the AaDα strains are more closely related to each other than to strains with the AαDa or AαDα genotypes (Figure 2). In addition, AFLP analysis identified two distinct AFLP genotypes among the AaDα isolates, and three distinctive AFLP genotypes among the AαDa isolates. The only AαDα isolate (nc5–19) had a unique AFLP genotype that was related to the AαDa strains (Figure 2). Both AFLP and MLST analyses suggest at least two, non-exclusive explanations for these data: Strains with identical MLST but distinct AFLP genotypes may have originated from multiple hybridization events between different serotype A and serotype D strains. Conversely, they may have originated from a single hybridization event, but their AFLP genotypes changed following evolution over subsequent generations. For example, some of the AD strains are diploid and others are aneuploid [16]. Therefore, different AFLP genotypes may reflect the loss of chromosomes after the initial hybridization or mitotic recombination and homozygosis. Because both populations of serotype A isolates and AD hybrids exhibit a high level of clonality, contemporary AD strains may be the descendents of a limited number of ancestral AD hybrid strains that proliferated clonally, or may have resulted from multiple hybridization events between clonal strains of serotype A and serotype D. MLST analyses using more loci and careful examination of the karyotypes of these strains are necessary to resolve this question.

Our data indicate that serotype A isolates from the VNB group are geographically restricted to sub-Saharan Africa, whereas AaDα strains that inherited their serotype A genomes from the VNB group are distributed globally. Geographic isolation may have contributed to the unique genetic composition of this Botswanan population. For example, a major portion of Botswana is the Kalahari Desert, which is noted for its remarkably hot, arid climate and high levels of UV radiation. These conditions are likely to deter the spread of VNB strains. This hypothesis is supported by our experiments demonstrating that VNB strains are hypersensitive to UV irradiation and that global AaDα strains of VNB origin are more resistant to UV irradiation and in some cases are more thermotolerant.

Several animal and plant hybrids have been shown to exhibit greater fitness than their parental genotypes in novel or perturbed habitats [1,2]. There are also several cases of the increased fitness of hybrid genotypes among phytopathogenic fungi and oomycetes [41,42]. For example, rapid expansion of interspecies hybrids of the rust fungi, Melampsora medusae and M. accidentalis, coincided with the introduction of a new poplar host to the habitat for these fungi, which suggests that these fungal hybrids are better adapted to this new host [7,41]. Similarly, the transmission of lethal infections of alders in Europe has been attributed to the emergence of heteroploid hybrids between Phytophthora cambivora and P. fragariae [4]. Therefore, it is possible that the abundance of the VNB AaDα hybrid strains of C. neoformans in the global population and scarcity of the VNB haploid strains outside Botswana may be attributed to the increased fitness of the hybrids, which enhanced their ability to propagate and disseminate to new environments.

Other explanations for the worldwide distribution of the hybrid strains are also possible. For example, global spread of AD hybrid strains from Botswana may be attributed to human activity and the creation of a novel habitat that reduced competition with the parental species. In particular, an association between C. neoformans and pigeons (Columbia livia) is well documented [8,19]. Pigeons were introduced into southern Africa during the period of 1500 to 1700 [43]. The increased availability of pigeon excreta, and perhaps the excreta of other domesticated animals, which are rich substrates for the growth of C. neoformans, may have contributed to the global expansion of AD hybrid strains. However, since our experiments demonstrated that all strains grow well on pigeon excreta in the laboratory, other factor(s) may yet be discovered that favor hybrid over haploid VNB strains. It is also possible that VNB isolates will be discovered outside of Africa. For example, if VNB strains were historically more abundant and only recently became restricted to Botswana, hybridization might have occurred outside sub-Saharan Africa. Future analyses of the population structure of the C. neoformans species complex will investigate this possibility.

This investigation confirmed previous observations that approximately half of the global isolates of AD hybrids contain the rare MATa serotype A allele ([16,18,39] and X. Lin, A. Litvintseva, K. Nielsen, S. Patel, A. Floyd, et al., unpublished data). We applied methods of AFLP genotyping and phylogenetic analysis of three genes to demonstrate that many AaDα strains possess serotype A genomes from the Botswanan population. We also demonstrated that AD hybrid strains are more resistant to UV irradiation and in some cases are more thermally resistant. These data suggest two hypotheses: (i) AaDα strains probably originated in sub-Saharan Africa from an intervarietal hybridization between isolates of serotype A from the VNB subpopulation and isolates of serotype D; and (ii) this hybridization resulted in increased fitness of the hybrid strain(s), which allowed it to colonize new ecological niches, spread beyond Africa, and populate the world.

Materials and Methods

Isolates of C. neoformans.

Twelve AD hybrid strains isolated from four countries were analyzed and compared with a subset of 45 previously described strains of serotype A (Table 1) [22]. Isolates were maintained on yeast extract-peptone-dextrose (YPD) agar medium (Difco, at 30 °C.


Genomic DNA was extracted from each isolate and the AFLP analysis was performed as described [28]. Only pronounced and reproducible bands were scored for the analyses of population structure. Polymorphic AFLP bands were defined as bands of the same size that were present in some, but not all, isolates. To assess the reproducibility of the AFLP method, DNA was extracted and the AFLP reactions and analyses were performed on at least two separate occasions for each isolate. In comparing replicate analyses, 92% of the AFLP bands were identical (unpublished data).


We previously developed MLST genotyping for serotype A strains using 12 loci ( However, for this investigation, we did not amplify and sequence all 12 MLST loci in the AD hybrids, because unlike strains of serotype A or D, which are haploid, the AD hybrids are diploid, and the primers amplified both serotype A and D alleles of the loci. To overcome this problem, we developed new serotype A–specific primers for three of the MLST loci: CAP10, GPD1, and URE1 (PCR primers and conditions are listed in Table 3). Each PCR mixture contained 32 μl of 1X PCR buffer, 2 mM MgCl2, 0.2 mM dNTPs, 1 μM each primer, 0.065 μl of iTaq DNA Polymerase (Bio-Rad,, and approximately 1 ng of genomic DNA. PCR products were purified using the QIAquick PCR purification kit (Qiagen, and sequenced using an ABI 3700 sequencer with Big Dye terminators (Applied Biosystems, PCR primers used for the amplification of the fragments were also used for sequencing.


Table 3.

PCR Primers


Mating type identification.

Mating type– and serotype-specific primers were used to confirm the mating type alleles of the AD hybrid strains. The primer pairs, which amplify portions of the STE20a or STE20α alleles of serotype A or D, are designated STE20Aa, STE20Aα, and STE20Da, respectively [25]. Since the primers that were previously designed to amplify a serotype D–specific portion of the STE20α gene failed to generate any product in the AD strains, we designed new PCR primers specific to a more conserved region of the STE20α gene of serotype D: STE20α-F: 5′-GTAAGTGCAAAGGACCCATCTC; and STE20α-R: 5′-TGATCC CCAAAGACCAAATATC. The PCR conditions for amplification were as follows: 94 °C for 5 min, followed by 30 cycles of 94 °C for 30 sec, 52 °C for 30 sec, and 72 °C for 1 min, followed by 7-min extension at 72 °C (PCR reactions were the same as those described for MLST). DNA sequences of the corresponding STE20α portions were obtained and compared with the DNA sequences in the typing strains, JEC21, serotype D [30], and H99, serotype A (C. neoformans H99 sequencing project, Duke Institute for Genome Sciences and Policy, Center for Applied Genomics and Technology,

Data analyses.

Sequences were automatically aligned using Sequncher 4.1 (Gene Codes Corporation,; the alignment was imported into MacClade 4.05 [44] and manually edited. Ambiguously aligned characters and gaps were excluded from the analysis. Optimal phylogenetic trees were constructed using maximum parsimony (MP) and Bayesian approaches. MP trees for the individual loci and for the combined data set were identified with heuristic searches based on 500 random sequence additions for each data set and implemented in PAUP version 4.0b10 [45].

Bayesian inferences were performed with MrBayes version 3.0B4 using a General Time Reversible model with a proportion of invariable sites and a gamma-shaped distribution of rates across sites (GTR+I+G) model of evolution [46]. Each Bayesian analysis consisted of two runs of 1,000,000 generations, each using the default uniform priors, and a sample frequency of 100. Likelihood scores of each sampled generation were plotted by using Excel (Microsoft, and visually analyzed; phylograms collected before the stationary phase was reached were discarded [47]. The phylograms remaining from both runs were combined, and a majority-rule consensus phylogram of each gene and for the combined data from all three genes were generated using PAUP and compared for topological congruence.

Construction of AaDα hybrid strains.

To construct AaDα hybrid strains in the bt65/bt88 and JEC21 background, ura5 mutants of strains bt65 and bt88 were obtained. Wild-type strains bt65 and bt88 were grown in liquid YPD, washed three times in sterile distilled water, and plated on 5-fluoroorotic acid (5-FOA) medium, which inhibits cells with a functional URA5 gene [32]. 5-FOA-resistant colonies were selected and tested on the yeast nitrogen base minimal medium (YNB, Difco). Isolates that showed no growth on YNB (Aa ura5) were mixed with cells of the XL342 (Dα ade2) strain of serotype D [33] and incubated on V8 agar medium in the dark at 22 °C. After coincubation for 24 h, cells were collected, washed, and spread on YNB minimal medium to select for prototrophic fusion products. The ploidy of prototrophic AaDα strains was confirmed by FACS analysis.

Ploidy determination by FACS.

Yeast cells were processed for flow cytometry as described previously [48]. Briefly, cells were harvested from YPD medium, washed once in PBS buffer, and fixed in 1 ml of 70% ethanol overnight at 4 °C. Fixed cells were washed once with 1 ml of NS buffer (10 mM Tris-HCl [pH 7.6]; 250 mM sucrose; 1 mM EDTA [pH 8.0]; 1 mM MgCl2; 0.1 mM CaCl2; and 0.1 mM ZnCl2) and then stained with propidium iodide (10 mg/ml) in 0.2 ml of NS buffer containing RNaseA (1 mg/ml) at 4 °C for 4–16 h. Then 0.05 ml of the stained cell preparation was diluted into 2 ml of 50 mM Tris-HCl (pH 8.0) and sonicated for 1 min. Flow cytometry was performed on 10,000 cells and analyzed on the FL1 channel of a Becton-Dickinson FACScan (

Sensitivity to UV irradiation.

The following strains were tested for their sensitivity to UV irradiation: (i) six wild-type AaDα hybrid strains; (ii) three AaDα hybrids obtained in the laboratory by fusing bt65/bt88 and JEC21 strains; (iii) four strains of serotype A from the VNB subpopulation, including the two strains (bt88 and bt65) that were most closely related to the probable serotype A progenitor of AaDα strains; and (iv) the representative haploid strain of serotype A (H99) and representative haploid strain of serotype D (JEC21). All strains were grown to logarithmic phase at 30 °C with constant agitation in the dark in low-glucose medium (0.1% glucose, 1.3 mM glycine, 2.2 mM KH2PO4, 0.1 mM MgSO4-7H2O, 0.3 μM thiamine, 2 nM biotin, [pH 5.6]) supplemented with DL-3,4-dihydroxyphenylalanine-(DL-DOPA, 20mg/l). Yeast cells were counted in a hemocytometer, all cultures were adjusted to the same cell concentration (5.5 × 107 CFU/ml), serial 10-fold dilutions were prepared, and 2.0 μl of each strain was spotted onto YPD agar plates (to assess sensitivity to the UV irradiation) and low-glucose agar plates supplemented with 200 mg/l DL-DOPA (to assess melanin production). The YPD plates were then irradiated with UV light at approximately 48 mJ/cm2 (24- and 30-second settings, UV Stratalinker 1800; Stratagene, [49], and all plates were incubated at 30 °C for 72 h. To provide a quantitative assessment of UV resistance for each strain, the highest dilutions that yielded colonies after treatment with UV were identified. For such dilution, the number of individual colonies within a spot on the YPD plate was counted.

Supporting Information

Accession Numbers

The GenBank (​x.html) accession numbers for the STE20 genes discussed in this paper are H99 serotype A (AF542529) and JEC21 serotype D (AF542531).

MLST genotyping for serotype A strains using 12 loci is under accession numbers DQ212527–DQ212692. Unique MLST sequence types were deposited under accession numbers EF625826–EF625831.


We thank Rameshwari Thakur (National Health Laboratory, Gaborone, Botswana) and Wiley A. Schell (Medical Mycological Research Laboratory, Duke University Medical Center) for providing strains, Kirsten Nielsen for providing pigeon excreta medium, Dmitri Kazmin for help with image processing, and Lisa Bukovnik for sequencing.

Author Contributions

APL, XL, JH, and TGM conceived and designed the experiments. APL, XL, and IT performed the experiments. APL analyzed the data. TGM contributed reagents/materials/analysis tools. APL and TGM wrote the paper.


  1. 1. Arnold ML, Hodges SA (1995) Are natural hybrids fit or unfit relative to their parents? Trends Ecol Evol 10: 67–71.
  2. 2. Seehausen O (2004) Hybridization and adaptive radiation. Trends Ecol Evol 19: 198–207.
  3. 3. Brasier C (2000) The rise of the hybrid fungi. Nature 405: 134–135.
  4. 4. Brasier CM, Kirk SA, Delcan J, Cooke DEL, Jung T, et al. (2004) Phytophthora alni sp. nov. and its variants: Designation of emerging heteroploid hybrid pathogens spreading on Alnus trees. Mycol Res 108: 1172–1184.
  5. 5. Moon CD, Craven KD, Leuchtmann A, Clement SL, Schardl CL (2004) Prevalence of interspecific hybrids amongst asexual fungal endophytes of grasses. Mol Ecol 13: 1455–1467.
  6. 6. Paoletti M, Buck KW, Brasier CM (2006) Selective acquisition of novel mating type and vegetative incompatibility genes via interspecies gene transfer in the globally invading eukaryote Ophiostoma novo-ulmi. Mol Ecol 15: 249–262.
  7. 7. Newcombe G, Stirling B, McDonald S, Bradshaw HD (2000) Melampsora x columbiana, a natural hybrid of M. medusae and M. accidentalis. Mycol Res 104: 261–274.
  8. 8. Casadevall A, Perfect JR (1998) Cryptococcus neoformans . Washington (D.C.): ASM Press. 549 p.
  9. 9. Kwon-Chun KJ, Boekhout T, Fell JW, Diaz M (2002) (1557) Proposal to conserve the name Cryptococcus gattii against C. hondurianus and C. bacillisporus (Basidiomycota, Hymenomycetes, Tremellomycetidae). Taxon 51: 804–806.
  10. 10. Kwon-Chung KJ, Varma A (2006) Do major species concepts support one, two or more species within Cryptococcus neoformans? FEMS Yeast Res 6: 574–587.
  11. 11. Xu J, Vilgalys R, Mitchell TG (2000) Multiple gene genealogies reveal recent dispersion and hybridization in the human pathogenic fungus Cryptococcus neoformans. Mol Ecology 9: 1471–1481.
  12. 12. Bovers M, Hagen F, Theelen B, Kuramae E, Boekhout T (2005) Multi-locus sequencing raises new questions in the Cryptococcus neoformans species complex. 6th International Conference on Cryptococcus and Cryptococcosis.
  13. 13. Taylor JW, Jacobson DM, Kroken S, Kasuga T, Geiser D, et al. (2000) Phylogenetic species recognition and species concepts in fungi. Fungal Genet Biol 31: 21–32.
  14. 14. Dromer F, Mathoulin-Pelissier S, Launay O, Lortholary O (2007) Determinants of disease presentation and outcome during Cryptococcosis: The CryptoA/D study. PLoS Med 4: e21.. doi:10.1371/journal.pmed.0040021.
  15. 15. Lin X, Heitman J (2006) The biology of the Cryptococcus neoformans species complex. Annu Rev Microbiol 60: 69–105.
  16. 16. Lengeler KB, Cox GM, Heitman J (2001) Serotype AD strains of Cryptococcus neoformans are diploid or aneuploid and heterozygous at the mating-type locus. Infect Immun 69: 115–122.
  17. 17. Xu J, Luo G, Vilgalys RJ, Brandt ME, Mitchell TG (2002) Multiple origins of hybrid strains of Cryptococcus neoformans with serotype AD. Microbiology 148: 203–212.
  18. 18. Cogliati M, Esposto MC, Clarke DL, Wickes BL, Viviani MA (2001) Origin of Cryptococcus neoformans var. neoformans diploid strains. J Clin Microbiol 39: 3889–3894.
  19. 19. Litvintseva AP, Kestenbaum L, Vilgalys R, Mitchell TG (2005) Comparative analysis of environmental and clinical populations of Cryptococcus neoformans. J Clin Microbiol 43: 556–564.
  20. 20. Tanaka R, Nishimura K, Imanishi Y, Takahashi I, Hata Y, et al. (2003) Analysis of serotype AD strains from F1 progenies between urease-positive- and negative-strains of Cryptococcus neoformans. Nippon Ishinkin Gakkai Zasshi 44: 293–297.
  21. 21. Cogliati M, Esposto MC, Tortorano AM, Viviani MA (2006) Cryptococcus neoformans population includes hybrid strains homozygous at mating-type locus. FEMS Yeast Res 6: 608–613.
  22. 22. Litvintseva AP, Thakur R, Vilgalys R, Mitchell TG (2006) Multilocus sequence typing reveals three genetic subpopulations of Cryptococcus neoformans var. grubii (serotype A), including a unique population in Botswana. Genetics 172: 2223–2238.
  23. 23. Kavanaugh LA, Fraser JA, Dietrich FS (2006) Recent evolution of the human pathogen Cryptococcus neoformans by inter-varietal transfer of a 14 gene fragment. Mol Biol Evol 23: 1879–1890.
  24. 24. Lengeler KB, Wang P, Cox GM, Perfect JR, Heitman J (2000) Identification of the MATa mating-type locus of Cryptococcus neoformans reveals a serotype A MATa strain thought to have been extinct. Proc Natl Acad Sci U S A 97: 14455–14460.
  25. 25. Nielsen K, Cox GM, Wang P, Toffaletti D, Perfect JR, et al. (2003) Sexual cycle of Cryptococcus neoformans var. grubii and virulence of congenic a and α isolates. Infect Immun 71: 4831–4841.
  26. 26. Viviani MA, Esposto MC, Cogliati M, Montagna MT, Wickes BL (2001) Isolation of a Cryptococcus neoformans serotype A MATa strain from the Italian environment. Med Mycol 39: 383–386.
  27. 27. Viviani MA, Nikolova R, Esposto MC, Prinz G, Cogliati M (2003) First European case of serotype A MATa Cryptococcus neoformans infection. Emerg Inf Diseas 9: 1179–1180.
  28. 28. Litvintseva AP, Marra RE, Nielsen K, Heitman J, Vilgalys R, et al. (2003) Evidence of sexual recombination among Cryptococcus neoformans serotype A isolates in sub-Saharan Africa. Euk Cell 2: 1162–1168.
  29. 29. Yan Z, Li X, Xu J (2002) Geographic distribution of mating type alleles of Cryptococcus neoformans in four areas of the United States. J Clin Microbiol 40: 965–972.
  30. 30. Loftus BJ, Fung E, Roncaglia P, Rowley D, Amedeo P, et al. (2005) The genome of the basidiomycetous yeast and human pathogen Cryptococcus neoformans. Science 307: 1321–1324.
  31. 31. Varma A, Edman JC, Kwon-Chung KJ (1992) Molecular and genetic analysis of URA5 transformants of Cryptococcus neoformans. Infect Immun 60: 1101–1108.
  32. 32. Kwon-Chung KJ, Varma A, Edman JC, Bennett JE (1992) Selection of ura5 and ura3 mutants from the two varieties of Cryptococcus neoformans on 5-fluoroorotic acid medium. J Med Vet Mycol 30: 61–69.
  33. 33. Sudarshan S, Davidson RC, Heitman J, Alspaugh JA (1999) Molecular analysis of the Cryptococcus neoformans ADE2 gene, a selectable marker for transformation and gene disruption. Fungal Genet Biol 27: 36–48.
  34. 34. Nosanchuk JD, Rudolph J, Rosas AL, Casadevall A (1999) Evidence that Cryptococcus neoformans is melanized in pigeon excreta: Implications for pathogenesis. Infect Immun 67: 5477–5479.
  35. 35. Nielsen K, De Obaldia AL, Heitman J (2007) Cryptococcus neoformans mates on pigeon guano: Implications for the realized ecological niche and globalization. Eukaryot Cell 6: 949–959.
  36. 36. Wang Y, Casadevall A (1994) Decreased susceptibility of melanized Cryptococcus neoformans to UV light. Appl Environ Microbiol 60: 3864–3866.
  37. 37. Wang Y, Casadevall A (1996) Susceptibility of melanized and nonmelanized Cryptococcus neoformans to the melanin-binding compounds trifluoperazine and chloroquine. Antimicrob Agents Chemother 40: 541–545.
  38. 38. Dadachova E, Bryan RA, Huang X, Moadel T, Schweitzer AD, et al. (2007) Ionizing radiation changes the electronic properties of melanin and enhances the growth of melanized fungi. PLoS ONE 2: e457.. doi:10.1371/journal.pone.0000457.
  39. 39. Xu J, Mitchell TG (2003) Comparative gene genealogical analyses of strains of serotype AD identify recombination in populations of serotypes A and D in the human pathogenic yeast Cryptococcus neoformans. Microbiology 149: 2147–2154.
  40. 40. Lin X, Hull CM, Heitman J (2005) Sexual reproduction between partners of the same mating type in Cryptococcus neoformans. Nature 434: 1017–1021.
  41. 41. Kohn LM (2005) Mechanisms of fungal speciation. Annu Rev Phytopathol 43: 279–308.
  42. 42. Schardl CL, Craven KD (2003) Interspecific hybridization in plant-associated fungi and oomycetes: A review. Mol Ecol 12: 2861–2873.
  43. 43. Long JL (1981) Introduced birds of the world: The worldwide history, distribution and influence of birds introduced to new environments. London: David & Charles. pp. 208–211.
  44. 44. Maddison WP, Maddison DR (1989) Interactive analysis of phylogeny and character evolution using the computer program MacClade. Folia Primatol (Basel) 53: 190–202.
  45. 45. Swofford DL (2002) PAUP*: Phylogenetic analysis using parsimony (and other methods), version 4.0b. Sunderland (Massachusetts): Sinauer Associates, Inc.
  46. 46. Huelsenbeck JP, Ronquist F (2001) MRBAYES: Bayesian inference of phylogenetic trees. Bioinformatics 17: 754–755.
  47. 47. Diezmann S, Cox CJ, Schonian G, Vilgalys RJ, Mitchell TG (2004) Phylogeny and evolution of medical species of Candida and related taxa: A multigenic analysis. J Clin Microbiol 42: 5624–5635.
  48. 48. Tanaka R, Taguchi H, Takeo K, Miyaji M, Nishimura K (1996) Determination of ploidy in Cryptococcus neoformans by flow cytometry. J Med Vet Mycol 34: 299–301.
  49. 49. Idnurm A, Heitman J (2005) Light controls growth and development via a conserved pathway in the fungal kingdom. PLoS Biol 3: e95.. doi:10.1371/journal.pbio.0030095.