Next Article in Journal
Comparative Genomics and Description of Putative Virulence Factors of Melissococcus plutonius, the Causative Agent of European Foulbrood Disease in Honey Bees
Next Article in Special Issue
Assessing Metagenomic Signals Recovered from Lyuba, a 42,000-Year-Old Permafrost-Preserved Woolly Mammoth Calf
Previous Article in Journal
Membrane Surface Features of Blastocystis Subtypes
Previous Article in Special Issue
Gut Microbiome and Putative Resistome of Inca and Italian Nobility Mummies
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Pathogen Species Identification from Metagenomes in Ancient Remains: The Challenge of Identifying Human Pathogenic Species of Trypanosomatidae via Bioinformatic Tools

1
IRD, Montpellier University, InterTryp, 34394 Montpellier, France
2
INRA-UMR 1062 CBGP (INRA, IRD, CIRAD), Montpellier SupAgro, Montferrier-sur-Lez, 34988 Languedoc Roussillon, France
3
Parasitology-Mycology Department, Avicenne Hospital, AP-HP, 93000 Bobigny, France
4
Montpellier University, IRD, CNRS, MIVEGEC, 34394 Montpellier, France
*
Authors to whom correspondence should be addressed.
Genes 2018, 9(8), 418; https://doi.org/10.3390/genes9080418
Submission received: 6 July 2018 / Revised: 8 August 2018 / Accepted: 16 August 2018 / Published: 20 August 2018

Abstract

:
Accurate species identification from ancient DNA samples is a difficult task that would shed light on the evolutionary history of pathogenic microorganisms. The field of palaeomicrobiology has undoubtedly benefited from the advent of untargeted metagenomic approaches that use next-generation sequencing methodologies. Nevertheless, assigning ancient DNA at the species level is a challenging process. Recently, the gut microbiome analysis of three pre-Columbian Andean mummies (Santiago-Rodriguez et al., 2016) has called into question the identification of Leishmania in South America. The accurate assignment would be important because it will provide some key elements that are linked to the evolutionary scenario for visceral leishmaniasis agents in South America. Here, we recovered the metagenomic data filed in the metagenomics RAST server (MG-RAST) to identify the different members of the Trypanosomatidae family that have infected these ancient remains. For this purpose, we used the ultrafast metagenomic sequence classifier, based on an exact alignment of k-mers (Kraken) and Bowtie2, an ultrafast and memory-efficient tool for aligning sequencing reads to long reference sequences. The analyses, which have been conducted on the most exhaustive genomic database possible on Trypanosomatidae, show that species assignments could be biased by a lack of some genomic sequences of Trypanosomatidae species (strains). Nevertheless, our work raises the issue of possible co-infections by multiple members of the Trypanosomatidae family in these three pre-Columbian mummies. In the three mummies, we show the presence of DNA that is reminiscent of a probable co-infection with Leptomonas seymouri, a parasite of insect’s gut, and Lotmaria.

1. Introduction

Santiago-Rodriguez et al. reported for the first time some evidence of the occurrence of Leishmania DNA in the guts of Andean mummies dating to pre-Columbian times, and they proposed an assignment to L. donovani [1]. In South America, the circulation of such Leishmania species is currently unknown, and has never before been documented in human remains. Therefore, the proper identification of the Leishmania species that would have infected mummies before Iberian colonization remains a major concern, and would bring new elements to the puzzle of the possible evolutionary scenarios [2]. L. donovani and L. infantum are by far the most common Leishmania species responsible for the visceral form (visceral leishmaniasis, VL) of the disease in both the Old World and the New World. So far, all of the cases of leishmaniasis described on pre-Columbian mummies are reminiscent of cutaneous (CL) or mucocutaneous (MCL) lesions: CL was observed on a mummy dating to a cultural group from 700–800 AD and found in a cemetery in Peru [3], and MCL was found on four samples in the archaeological cemetery of Coyo Oriente (skulls approximately 1000 years old) located in the desert of San Pedro de Atacama, Northern Chile [4]. These sites come from a time period predating European contacts. A Leishmania infection was confirmed in these remains using a Polymerase chain reaction (PCR) approach [4] (amplification of fragments of the inositol monophosphate dehydrogenase gene, the kinetoplast minicircle, the amino acid permease AAP13LD, and the adenylate kinase gene). Furthermore, the amplified sequences differed from those of L. donovani.
The rise of NGS (next-generation sequencing) technologies has opened a new field of systematic investigations in metagenomics. When these new technologies are applied to samples of ancient human remains, they provide valuable information to scientists working on the evolutionary history of infectious diseases. To avoid environmental contamination and accurately authenticate ancient DNA, a number of precautions and rules have been enacted [5,6]. Among them: (i) the requirement of a dedicated ancient DNA laboratory to minimize and manage contamination, particularly during sample collection, and the risk of exogenous DNA contaminations from the laboratory; and (ii) microbial ancient DNA damage should exhibit patterns of DNA damage and fragmentation; nevertheless, these patterns vary according to source context and species, but also according to the workflow and enzymes used during library preparation. The characterization of gut microbiomes of pre-Columbian mummies by Santiago-Rodriguez et al. using unbiased metagenomic approaches gave the opportunity to detect traces of specific pathogens [1]. Nevertheless, several issues have been raised regarding the age of sequenced DNA and the possibility of environmental contaminations [7,8]. The answer to these questions has been published [9]. However, if environmental contamination is a crucial problem when working on bacteria, for human pathogenic Trypanosomatidae, environmental contamination is unlikely to occur. Indeed, these parasitic eukaryotes require an adequate environment to survive and proliferate. They are not free-living microorganisms, and have not had the ability to survive very long outside their hosts. Thus, contamination with such organisms is unlikely to occur during manipulation and the laboratory processing of samples. DNA contamination of the mummies by contact with some infected insects that transmit them (sandfly, Psychodidae-Phlebotominae, for Leishmania or Triatoma, Reduviidae-Triatominae, for Trypanosoma cruzi) cannot be ruled out. Thus, because of the very low probability of such contamination, the available metagenomic data [1] are of great interest to detect the presence of parasites belonging to the Trypanosomatidae familly in these ancient remains.
Basic Local Alignment Search Tool (BLAST) alignments, which rely on finding the best alignment to a panel of genomic sequences, were often the traditional approach to assign a taxonomic label to an unknown sequence. However, unambiguous assignment at the species level is very hard, and this tool is very expensive in central processing unit (CPU) time for NGS data analysis on local computers, even if new facilities are now available via the use of Cloud public infrastructure or computer cluster. To shed light on the causative agent of leishmaniasis infection (and more broadly on parasites belonging to the Trypanosomatidae family) in these ancient remains, we used new software dedicated to metagenomic data analysis. Kraken, a bioinformatic program [10], presents numerous advantages over other programs, including its speed of performing analysis on metagenomes. The identification at the species level by Kraken is based on the use of exact-match database queries of k-mers, rather than on alignment similarity. This new approach was applied to the metagenomic rapid annotation using subsystems technology (MG-RAST) pre-processed metagenomic data [1], and the results were compared to those obtained with Bowtie2 [11].

2. Materials and Methods

2.1. Data

The metagenomic data that we used of the gut microbiomes from three pre-Columbian Andean mummies (FI3, FI9, and FI12) were available in the MG-RAST server (http://blog.mg-rast.org/) (MGRAST IDs 4629033.3, 4630170.3 and 4626489.3, respectively).
We built a reference genome database composed of all of the complete Trypanosomatidae genomes collected from the NCBI (http://www.ncbi.nlm.nih.gov/genome/) and complemented by genomes from TriTrypDB release 37 (25 April 2018) (Kinetoplastid Genomics Resource http://tritrypdb.org/tritrypdb/) [12]. The total number of Trypanosomatidae genomes in the database is 79 (Table S1).

2.2. Methods

We analyzed the data with Kraken (version 1.0), which is a system for ultrafast metagenomic sequence classification using exact alignment [10] (http://ccb.jhu.edu/software/kraken/). It relies on the development of a database that contains records consisting of a k-mer and the lowest common ancestor (LCA) of all of the organisms whose genomes contain that k-mer [10]. We built a reference database with the default parameters of Kraken (k = 31). We downloaded the pre-processed sequences (this step filters sequences based on length, the number of ambiguous bases, and quality value) from the MG-RAST server, and then compared them with the non-redundant, custom-built Trypanosomatidae database. The results were visualized with a metagenomic visualization tool, Krona [13]. To complete the analysis, the same set of metagenome data was analyzed with Bowtie2—a program for the rapid alignment of gapped reads—using the sensitive option [11]. To extract the coverage from the Binary Alignment Map (BAM) alignment files, we used the samtools program version 1.08, command idxstats [14]. The reference genome database was used for analyses conducted with the two methodologies.

3. Results and Discussion

In a first attempt to compare the respective limits of the two tools in the species assignment, we focused on microorganisms belonging to the Trypanosomatidae family. These were chosen for two reasons: first, because reported Leishmania infection is already reported in some mummies [1], and second, because of the endemicity of Chagas disease [15] and leishmaniasis in this South American region [16].
We conducted analyses for the three mummies on pre-processed data, as indicated in the methods section. To confirm that the detected traces of Trypanosomatidae DNA are not the result of environmental contaminations, we used the data passed through the screening step (i.e., following the dereplication and the duplicate read inferred sequencing error estimation (DRISEE) steps) in MG-RAST. The results confirmed clearly a co-infection with at least two pathogenic Trypanosomatids and the fact that is not the result of a contamination

3.1. Trypanosomes and Chagas Disease

The genome representativity of our database is 55% (11 genomes out of approximately 20 Trypanosoma species currently described) (Figure 1A). The reference database includes trypanosomes responsible for American trypanosomiasis (T. cruzi) and trypanosomes responsible for human African trypanosomiasis and animal trypanosomiasis.
The analysis performed with Kraken reveals that a non-negligible proportion of reads (5%, 9%, and 10% for FI3, FI9, and FI12) is attributed to the Trypanosomatidae family (Figure 2A). The genus Trypanosoma is clearly identified in ancient DNA from the guts of the three mummies FI3, FI9, and FI12, with 63%, 69%, and 52% of the detected Trypanosomatidae community, respectively (Figure 2B). As expected, almost all of the reads belonging to the genus Trypanosoma can be attributed to T. cruzi (Figure 3A–C) for the three mummies. These results corroborate the conclusion of Santiago-Rodriguez et al. [1]. Currently, T. cruzi is split into six genetic lineages or discrete typing units (DTUs) named TcI, TcIV, TcII, TcIII, TcV, and TcVI, respectively, and a seventh one called TcBat. For both FI3 and FI9, the highest number of reads matches the T. cruzi strain Tula cl2 (Table S2), which belongs to TcI (DTU I). This DTU is widely represented in the genomic database that we gathered (five of the 11 genomes currently available). For FI12, reads that match Tula cl2 are scarce (Table S2). Nevertheless, because of the relatively low proportion (<10%) of reads that match with a genome filed in our database, it is probable that the DTU of the infecting T. cruzi strain is not yet represented.
Analysis with Bowtie2 clearly confirmed a T. cruzi infection (53%, 49%, and 57% for FI3, FI9, and FI12, respectively) in these mummies (Figure 2C). The majority of reads matched T. cruzi strains Y and Tula cl2 (Table S3) rather than other genomes filed in the database. Concerning the alignment with T. cruzi Y, the reads matched 178 and 203 contigs in FI3 and FI9, respectively, out of 9821 (Table S4). A large majority of reads (80% in FI3 and 90% in FI9) matched 52 identical contigs for both mummies. For T. cruzi Tula cl2, reads of mummy FI3 and mummy FI9 matched 42 and 39 contigs, respectively, out of 5300, and almost 100% of the reads for both mummies matched 28 identical contigs (Table S4). Overall, this set of results indicates that the infecting T. cruzi strain is probably not in our reference database.
Most of the genomes of T. cruzi strains are lacking: currently, only 11 complete genomes are available in the NCBI and/or TriTrypDB databases out of more than 1902 deposited strains to date [17]. Likewise, the database we used contains no representative genomes belonging to DTUs III, IV, or VII (TcBat). Interestingly, ancient T. cruzi DNA has also been identified in human mummies dating from the same period (Chinchorro culture) and in the same geographical region, Southern Peru [18]. In Bolivia and Peru, strains belonging to the DTU I and DTU V clades are the main T. cruzi strains isolated, followed by strains of DTUs IV, III, and VI [15]. The knowledge of the complex evolutionary history of T. cruzi, which involved genetic exchanges [19], and the existence of hybrid DTUs will certainly benefit from the identification of the infecting strains at the DTU level from this ancient DNA material. Insight into the circulating strains in these mummies should generate important elements for the calibration of such a dynamically evolving scenario. Nevertheless, our analysis highlights that the ancient T. cruzi DNA present in the three mummies cannot be assigned to T. cruzi CL Brener (DTU VI).

3.2. Leishmania and Leishmaniasis

All of the Leishmania genomes that are currently available in NCBI or in TriTrypDB are included in the reference database. The database represents only 38% of genomes from 21 of the 54 Leishmania species that have been currently identified [20]. Microorganisms from the subgenera Leishmania and Viannia are well represented (Figure 1B). Human pathogenic Leishmania spp. are far better represented in the database (14/20), with the subgenera Leishmania and Viannia well represented (80% and 83%, respectively). No genome from the subgenus Porcisia (Paraleishmania section) is available (Table 1). This subgenus includes some human pathogenic Leishmania sp., such as L. colombiensis.
The NGS reads analyzed with the metagenomic sequence classifier Kraken highlight a probable co-infection with a Leishmania parasite for the three mummies FI3, FI9, and FI12 (Figure 2B), with 3%, 3%, and 10% of the reads attributed to Trypanosomatidae that belong to the genus Leishmania, respectively. From Figure 3, it is clear that Kraken assigns reads to a large number of Leishmania species, each with a low percentage. Clearly, no predominant Leishmania spp. is detected, and L. donovani does not appear as a probable infecting Leishmania species in all of these mummies. Therefore, these results prompt us to question the Leishmania species infecting the mummies. Since DNA originates from internal tissues, we have to look for the Leishmania spp. That are currently known to affect mainly internal organs and cause VL, namely, L. donovani, L. infantum, L. tropica, L. martiniquensis, and L. colombiensis. At this point, we can exclude an infection by the first four L. species cited above. The sequence of the L. colombiensis genome (Paraleishmania section) is currently not available, and may be the Leishmania agent that we are seeking. Currently, in Peru, the country from which mummies originate, Leishmania pathogens for humans include L. peruviana, L. guyanensis, L. amazonensis, L. lainsoni, and L. braziliensis [20]. Some Leishmania species that usually cause cutaneous forms have, under some circumstances, the capacity to disseminate into internal organs [21,22]. Such unusual clinical presentation is frequently associated with an immunocompromised state or dysfunction of the T helper-mediated immune response [2]. Our study clearly shows that a low proportion of reads are attributed to L. peruviana, L. amazonensis, L. braziliensis, and L. guyanensis (species causing CL). Such low frequency in read assignment calls into question the validity of the identification (Figure 2) (Table S2). Nevertheless, the occurrence of an infection by multiple Leishmania sp. cannot be ruled out as well as infection by hybrid strains of Leishmania [20]. From these results, it is clear that to be accurate in its species assignment, the reference database used by Kraken needs to be highly representative of the described species and strains. The more exhaustive the database, the better the assignment accuracy will be.
The alignment program Bowtie2 detects the presence of Leishmania in three mummies (FI3, FI9, and FI12) (Figure 2C). However, unlike the mummy FI12, in the mummies FI3 and FI9, the reads match a large panel of Leishmania sp., especially in the mummy FI3 (Table S3). Then, it is not possible to unequivocally assign DNA to a specific Leishmania species and L. donovani in particular due to the number of genomes of different Leishmania spp. matched.
Our analysis reveals that the genome of the infecting Leishmania species, whose DNA is detected in these ancient remains, is probably not present in our reference database. We may consider the occurrence of an ancient Leishmania species. Nevertheless, since our reference database is not exhaustive, we cannot rule out the presence of Leishmania sp. causing CL or MCL or the co-infection of multiple Leishmania spp. Still, the detection of Leishmania DNA is clearly not the result of an artefact or a contamination.

3.3. Other Leishmaniinae (Crithidiatae)

Trypanosoma and Leishmania are dixenous parasites, meaning that their life cycle includes an invertebrate as a first host and a vertebrate as a second host. Several genomes of monoxenous (one-host) Trypanosomatidae are available and belong to the genera Angomonas, Crithidia, Leptomonas, Lotmaria, and Strigomonas (Table S1). The database genome representativity for Leptomonas is 5%, with only two genomes available out of the 39 Leptomonas species currently described (Figure 1C). The analysis performed on the three mummies revealed that a relatively high proportion of reads attributed to the family Trypanosomatidae is reminiscent of the genus Leptomonas (13%, 18%, and 13% for F13, FI9, and FI12, respectively) (Figure 2B). A large majority of these reads are assigned to L. seymouri and not L. pyrrochoris after an analysis with Kraken (Figure 3A–C) (Table S2). Nevertheless, because of the lack of available genomes for 37 out of 39 Leptomonas sp., the assignment to L. seymouri has to be taken with caution, and an assignment at the strain level cannot be made.
Bowtie2 also confirms the recurrent occurrence of L. seymouri in all of the mummies (Figure 2C), and a high number of reads match the L. seymouri strain BHU-1095 (Table S3) in mummies FI3 and FI9 (56,245 and 125,577, respectively). In both mummies, the reads match with eight and nine scaffolds (out of 1216), respectively, and a large majority of reads match on only five scaffolds (Table S4). Leptomonas species are usually found in the gut of insects, but they have the potential to infect mammals as an opportunistic parasite. Nevertheless, their infective capacity in mammals seems to be limited to immunocompromised hosts [23]. Interestingly, L. seymouri has been repeatedly isolated from VL patients infected by L. donovani in India [24].
To our surprise, the analysis performed with Kraken reveals that an equivalent proportion of reads (2%) is assigned to L. passim in the three mummies (Figure 2B and Figure 3). Via Bowtie2 analysis, a very low number of reads matches this genus in the mummies (Figure 2C and Table S3). L. passim is the founding member of this genus (Figure 1). This member of Crithidiatae is described as a common parasite of the honey bee Apis mellifera [25], which calls into question its presence in a human gut microbiome.

4. Conclusions

The strength of our approach is to work with the most exhaustive reference database of Trypanosomatidae genomic sequences that are possible, combined with two programs that are complementary in their metagenomic analysis approaches (k-mer searching versus local alignment). These allowed us to gain insight into the identity of the infecting Trypanosomatidae agent. Analysis using the sequence classifier (Kraken) unambiguously confirmed T. cruzi infection and undoubtedly Leishmania infection in the three Andean mummies. In addition, our analysis provides new information on co-infection by at least two human pathogenic trypanosomatids, Leishmania spp. and T. cruzi, in all of the mummies with available metagenomes. This type of co-infection is known to occur in humans as well as in some wild mammals [26,27]. Unfortunately, it is not possible to go further in the assignment to the species level for Leishmania and DTU level for T. cruzi. This may be due to the lack of a number of Leishmania genomes, particularly those of the Paraleishmania section, and of members of T. cruzi belonging to some DTUs. It also highlights a pattern of polyinfection coupled with an opportunistic trypanosomatid, i.e., L. seymouri [28]. Therefore, future studies with an exhaustive reference database are necessary to better understand the interrelationships that shape the microbial community and play a role in the evolution of the parasitome.

Supplementary Materials

The following are available online at https://www.mdpi.com/2073-4425/9/8/418/s1, Table S1: List of Trypanosomatidae genome sequences available and included in the reference database. Table S2. (A) Results of Kraken analysis on preprocessed metagenomic data for the mummy FI3 (mgm_46.29033.3); (B) results of Kraken analysis on preprocessed metagenomic data for the mummy FI9 (mgm_46.30170.3); (C) results of Kraken analysis on preprocessed metagenomic data for the mummy FI12 (mgm_46.26489.3); Table S3. Results of Bowtie2 analysis concerning the three mummies FI3, FI9 and FI12. Table S4. Distribution of reads matching (a) Leptomonas seymouri, (b) Trypanosoma cruzi Y and (c) Trypanosoma cruzi Tula cl2 on the contigs for the three mummies.

Author Contributions

Writing-Original Draft Preparation, P.P. and D.S.; Bioinformatic analyses, F.D.; Writing-Review & Editing, P.P., D.S., F.D. and M.A.

Funding

The authors received no specific funding for this work.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Santiago-Rodriguez, T.M.; Fornaciari, G.; Luciani, S.; Dowd, S.E.; Toranzos, G.A.; Marota, I.; Cano, R.J. Taxonomic and predicted metabolic profiles of the human gut microbiome in pre-Columbian mummies. FEMS Microbiol. Ecol. 2016, 92. [Google Scholar] [CrossRef] [PubMed]
  2. Sereno, D.; Akhoundi, M.; Dorkeld, F.; Oury, B.; Momen, H.; Perrin, P. What pre-Columbian mummies could teach us about South American leishmaniases? Pathog. Dis. 2017, 75. [Google Scholar] [CrossRef] [PubMed]
  3. Gerszten, E.; Allison, M.J.; Maguire, B. Paleopathology in South American mummies: A review and new findings. Pathobiology 2012, 79, 247–256. [Google Scholar] [CrossRef] [PubMed]
  4. Costa, M.A.; Matheson, C.; Lachetta, L.; Llagostera, A.; Appenzeller, O. Ancient leishmaniasis in a highland desert of Northern Chile. PLoS ONE 2009, 4. [Google Scholar] [CrossRef] [PubMed]
  5. Salter, S.J.; Cox, M.J.; Turek, E.M.; Calus, S.T.; Cookson, W.O.; Moffatt, M.F.; Turner, P.; Parkhill, J.; Loman, N.J.; Walker, A.W. Reagent and laboratory contamination can critically impact sequence-based microbiome analyses. BMC Biol. 2014, 12, 87. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  6. Warinner, C.; Herbig, A.; Mann, A.; Fellows Yates, J.A.; Weir, C.L.; Burbano, H.A.; Orlando, L.; Krause, J. A robust framework for microbial archaeology. Annu. Rev. Genom. Hum. Genet. 2017, 18, 321–356. [Google Scholar] [CrossRef] [PubMed]
  7. Eisenhofer, R.; Cooper, A.; Weyrich, L.S. Reply to Santiago-Rodriguez et al.: Proper authentication of ancient DNA is essential. FEMS Microbiol. Ecol. 2017, 93. [Google Scholar] [CrossRef] [PubMed]
  8. Eisenhofer, R.; Weyrich, L.S. Proper authentication of ancient DNA is still essential. Genes 2018, 9. [Google Scholar] [CrossRef] [PubMed]
  9. Toranzos, G.A.; Santiago-Rodriguez, T.M.; Cano, R.J.; Fornaciari, G. Proper authentication of ancient DNA is essential, yes; but so are undogmatic approaches. FEMS Microbiol. Ecol. 2017, 93. [Google Scholar] [CrossRef] [PubMed]
  10. Wood, D.E.; Salzberg, S.L. Kraken: Ultrafast metagenomic sequence classification using exact alignment. Genome Biol. 2014, 15. [Google Scholar] [CrossRef] [PubMed]
  11. Langmead, B.; Salzberg, S.L. Fast gapped-read alignment with Bowtie2. Nat. Methods 2012, 9, 357–359. [Google Scholar] [CrossRef] [PubMed]
  12. Aslett, M.; Aurrecoechea, C.; Berriman, M.; Brestelli, J.; Brunk, B.P.; Carrington, M.; Depledge, D.P.; Fischer, F.; Gajria, B.; Gao, X.; et al. TriTrypDB: A functional genomic resource for the Trypanosomatidae. Nucl. Acids Res. 2010, 38, D457–D462. [Google Scholar] [CrossRef] [PubMed]
  13. Ondov, B.D.; Bergman, N.H.; Phillippy, A.M. Interactive metagenomic visualization in a Web browser. BMC Bioinform. 2011, 12, 385. [Google Scholar] [CrossRef] [PubMed]
  14. Li, H.; Handsaker, B.; Wysoker, A.; Fennell, T.; Ruan, J.; Homer, N.; Marth, G.; Abecasis, G.; Durbin, R.; 1000 Genome Project Data Processing Subgroup. The sequence alignment/map (SAM) format and SAMtools. Bioinformatics 2009, 25, 2078–2079. [Google Scholar] [CrossRef] [PubMed]
  15. World Health Organization. Fact Sheet on Chagas Disease. Available online: http://www.who.int/chagas/resources/en/ (accessed on 15 April 2018).
  16. World Health Organization. Fact Sheet on Leishmaniasis. Available online: http://www.who.int/leishmaniasis/resources/en/ (accessed on 15 April 2018).
  17. Brenière, S.F.; Waleckx, E.; Barnabé, C. Over six thousand Trypanosoma cruzi strains classified into discrete typing units (DTUs): Attempt at an inventory. PLoS Negl. Trop. Dis. 2016, 10. [Google Scholar] [CrossRef] [PubMed]
  18. Aufderheide, A.C.; Salo, W.; Madden, M.; Streitz, J.; Buikstra, J.; Guhl, F.; Arriaza, B.; Renier, C.; Wittmers, L.E., Jr.; Fornaciari, G.; et al. A 9000-year record of chagas’ disease. Proc. Natl. Acad. Sci. USA 2004, 101, 2034–2039. [Google Scholar] [CrossRef] [PubMed]
  19. Tomasini, N.; Diosque, P. Evolution of Trypanosoma cruzi: Clarifying hybridisations, mitochondrial introgressions and phylogenetic relationships between major lineages. Mem. Inst. Oswaldo Cruz 2015, 110, 403–413. [Google Scholar] [CrossRef] [PubMed]
  20. Akhoundi, M.; Downing, T.; Votypka, J.; Kuhls, K.; Lukes, J.; Cannet, A.; Ravel, C.; Marty, P.; Delaunay, P.; Kasbari, M.; et al. Leishmania infections: Molecular targets and diagnosis. Mol. Asp. Med. 2017, 57, 1–29. [Google Scholar] [CrossRef] [PubMed]
  21. Barral, A.; Badaro, R.; Barral-Netto, M., Jr.; Grimaldi, G.; Momen, H.; Carvalho, E.M. Isolation of Leishmania mexicana amazonensis from the bone marrow in a case of American visceral leishmaniasis. Am. J. Trop. Med. Hyg. 1986, 35, 732–734. [Google Scholar] [CrossRef] [PubMed]
  22. Barral, A.; Pedral-Sampaio, D., Jr.; Grimaldi, G.; Momen, H.; MacMahon-Pratt, D.; Ribeiro de Jesus, A.; Almeida, R.; Badaro, R.; Barral-Netto, M.; Carvalho, E.M.; et al. Leishmaniasis in Bahia, Brazil: Evidence that Leishmania amazonensis produces a wide spectrum of clinical diseases. Am. J. Trop. Med. Hyg. 1991, 44, 536–546. [Google Scholar] [CrossRef] [PubMed]
  23. Kraeva, N.; Butenko, A.; Hlavacova, J.; Kostygov, A.; Myskova, J.; Grybchuk, D.; Lestinova, T.; Votypka, J.; Volf, P.; Opperdoes, F.; et al. Leptomonas seymouri: Adaptations to the dixenous life cycle analyzed by genome sequencing, transcriptome profiling and co-infection with Leishmania donovani. PLoS Pathog. 2015, 11. [Google Scholar] [CrossRef] [PubMed]
  24. Ghosh, S.; Banerjee, P.; Sarkar, A.; Datta, S.; Chatterjee, M. Coinfection of Leptomonas seymouri and Leishmania donovani in Indian leishmaniasis. J. Clin. Microbiol. 2012, 50, 2774–2778. [Google Scholar] [CrossRef] [PubMed]
  25. Tritschler, M.; Retschnig, G.; Yañez, O.; Williams, G.R.; Neumann, P. Host sharing by the honey bee parasites Lotmaria passim and Nosema ceranae. Ecol. Evol. 2017, 7, 1850–1857. [Google Scholar] [CrossRef] [PubMed]
  26. da Costa, A.P.; Costa, F.B.; Soares, H.S.; Ramirez, D.G.; Mesquita, E.T.; Gennari, S.M.; Marcili, A. Trypanosoma cruzi and Leishmania infantum chagasi infection in wild mammals from Maranhão state, Brazil. Vector Borne Zoonotic Dis. 2015, 15, 656–666. [Google Scholar] [CrossRef] [PubMed]
  27. Martínez, D.Y.; Verdonck, K.; Kaye, P.M.; Adaui, V.; Polman, K.; Llanos-Cuentas, A.; Dujardin, J.C.; Boelaert, M. Tegumentary leishmaniasis and coinfections other than HIV. PLoS Negl. Trop. Dis. 2018, 12. [Google Scholar] [CrossRef] [PubMed]
  28. Dedet, J.P.; Pratlong, F. Leishmania, Trypanosoma and monoxenous Trypanosomatids as emerging opportunistic agents. J. Eukaryot. Microbiol. 2000, 47, 37–39. [Google Scholar] [CrossRef] [PubMed]
Figure 1. Proportion of available genomes (in blue) on the number of currently named species (in red) for the various genera belonging to the Trypanosomatidae family. (A) genus Trypanosoma; (B) genus Leishmania; (C) other Trypanosomatidae genera.
Figure 1. Proportion of available genomes (in blue) on the number of currently named species (in red) for the various genera belonging to the Trypanosomatidae family. (A) genus Trypanosoma; (B) genus Leishmania; (C) other Trypanosomatidae genera.
Genes 09 00418 g001
Figure 2. Composition of gut microbiota for the three Andean mummies studied by Santiago-Rodriguez et al. [1]: FI3, FI9, and FI12, respectively. (A) Proportion of reads assigned to the Trypanosomatidae family for each mummy after analysis with Kraken. Reads not matching Trypanosomatidae sequences appear in grey. Reads matching Trypanosomatidae sequences are flesh colored; (B) In Trypanosomatidae: numbers and percentages of reads assigned to the genera Trypanosoma (purple), Leishmania (blue), Leptomonas (red), Lotmaria (green). Reads from mummies FI3, FI9, and FI12 matching to any other Trypanosomatidae are shown in orange; (C) Results obtained by the Bowtie2 alignment sequence for mummies FI3, FI9, and FI12, respectively. For facility in comparison of the results gathered with both software the same color reference was used.
Figure 2. Composition of gut microbiota for the three Andean mummies studied by Santiago-Rodriguez et al. [1]: FI3, FI9, and FI12, respectively. (A) Proportion of reads assigned to the Trypanosomatidae family for each mummy after analysis with Kraken. Reads not matching Trypanosomatidae sequences appear in grey. Reads matching Trypanosomatidae sequences are flesh colored; (B) In Trypanosomatidae: numbers and percentages of reads assigned to the genera Trypanosoma (purple), Leishmania (blue), Leptomonas (red), Lotmaria (green). Reads from mummies FI3, FI9, and FI12 matching to any other Trypanosomatidae are shown in orange; (C) Results obtained by the Bowtie2 alignment sequence for mummies FI3, FI9, and FI12, respectively. For facility in comparison of the results gathered with both software the same color reference was used.
Genes 09 00418 g002
Figure 3. Profiles of microbiomes from three Andean mummies [1]: FI3, FI9, and FI12, for Trypanosomatidae. Circles represent taxonomic classification in ascending order up to the species level (outermost circle) with their relative abundance. These graphs were generated using the program Krona. Less abundant taxa are listed outside the charts.
Figure 3. Profiles of microbiomes from three Andean mummies [1]: FI3, FI9, and FI12, for Trypanosomatidae. Circles represent taxonomic classification in ascending order up to the species level (outermost circle) with their relative abundance. These graphs were generated using the program Krona. Less abundant taxa are listed outside the charts.
Genes 09 00418 g003aGenes 09 00418 g003bGenes 09 00418 g003c
Table 1. Representativity of sequenced genomes available in relation to the number of known Leishmania species that are pathogenic for humans, according the updated classification of Akhoundi et al. (2017) [18].
Table 1. Representativity of sequenced genomes available in relation to the number of known Leishmania species that are pathogenic for humans, according the updated classification of Akhoundi et al. (2017) [18].
LeishmaniaVianniaSauroleishmaniaMundiniaL. australiensis
(L. macropodum)
PorcisiaEndotrypanum
Number of species pathogenic for humans10601120
Number of genomes available8501000
Representativity in %80830100000

Share and Cite

MDPI and ACS Style

Sereno, D.; Dorkeld, F.; Akhoundi, M.; Perrin, P. Pathogen Species Identification from Metagenomes in Ancient Remains: The Challenge of Identifying Human Pathogenic Species of Trypanosomatidae via Bioinformatic Tools. Genes 2018, 9, 418. https://doi.org/10.3390/genes9080418

AMA Style

Sereno D, Dorkeld F, Akhoundi M, Perrin P. Pathogen Species Identification from Metagenomes in Ancient Remains: The Challenge of Identifying Human Pathogenic Species of Trypanosomatidae via Bioinformatic Tools. Genes. 2018; 9(8):418. https://doi.org/10.3390/genes9080418

Chicago/Turabian Style

Sereno, Denis, Franck Dorkeld, Mohammad Akhoundi, and Pascale Perrin. 2018. "Pathogen Species Identification from Metagenomes in Ancient Remains: The Challenge of Identifying Human Pathogenic Species of Trypanosomatidae via Bioinformatic Tools" Genes 9, no. 8: 418. https://doi.org/10.3390/genes9080418

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop