A comparative molecular and 3-dimensional structural investigation into cross-continental and novel avian Trypanosoma spp. in Australia
© The Author(s). 2017
Received: 9 February 2017
Accepted: 3 May 2017
Published: 12 May 2017
Molecular and structural information on avian Trypanosoma spp. throughout Australia is limited despite their intrinsic value in understanding trypanosomatid evolution, diversity, and structural biology. In Western Australia tissue samples (n = 429) extracted from 93 birds in 25 bird species were screened using generic PCR primers to investigate the diversity of Trypanosoma spp. To investigate avian trypanosome structural biology the first 3-dimensional ultrastructural models of a Trypanosoma spp. (Trypanosoma sp. AAT) isolated from a bird (currawong, Strepera spp.) were generated using focussed ion beam milling combined with scanning electron microscopy (FIB-SEM).
Here, we confirm four intercontinental species of avian trypanosomes in native Australian birds, and identify a new avian Trypanosoma. Trypanosome infection was identified in 18 birds from 13 different bird species (19%). A single new genotype was isolated and found to be closely related to T. culicavium (Trypanosoma sp. CC2016 B002). Other Trypanosoma spp. identified include T. avium, T. culicavium, T. thomasbancrofti, Trypanosoma sp. TL.AQ.22, Trypanosoma sp. AAT, and an uncharacterised Trypanosoma sp. (group C-III sensu Zidková et al. (Infect Genet Evol 12:102-112, 2012)), all previously identified in Australia or other continents. Serially-sectioning Trypanosoma sp. AAT epimastigotes using FIB-SEM revealed the disc-shaped kinetoplast pocket attached perpendicular to the branching mitochondrion. Additionally, the universal minicircle sequence within the kinetoplast DNA and the associated binding protein were determined in Trypanosoma sp. AAT.
These results indicate that bird trypanosomes are relatively conserved across continents, while being locally diverse, which supports the hypothesis that bird trypanosomes exist as fewer species than described in the literature. Evidence exists that avian Trypanosoma spp. are infecting mammals and could be transmitted by haemadipsid leeches. Trypanosoma sp. AAT is most likely a separate species currently found only in Australia and the first 3-dimentional ultrastructural analysis of an avian trypanosome provides interesting information on their morphology and organelle arrangement.
Parasites from the genus Trypanosoma are protozoan flagellates that infect almost all known animal taxa and are responsible for a number of neglected diseases in humans and livestock. The biodiversity and biology of trypanosomes infecting wildlife worldwide is still an area that is poorly understood, especially in birds. The prevalence of bird trypanosomes is difficult to assess accurately because of low parasitaemia, morphological tropism in the host, and development in the bone marrow rather than peripheral blood [1–3]. In the past, avian trypanosomes were often presumed to be species-specific, which resulted in the description of almost 100 species. As early as 1974 researchers proposed the actual number of species present in birds was likely to be much lower and that the taxonomic descriptions of avian trypanosomes should be revised [4–6]. Researchers suggested that investigating blood smears taken from birds to identify trypanosomes was outlasting its usefulness, despite being the most popular method of screening for trypanosome infection . Recent phylogenetic analyses of bird trypanosomes indicate there are less bird trypanosomes than currently described and the majority most likely belong to one of three trypanosome species (Trypanosoma corvi, Trypanosoma avium or Trypanosoma bennetti) with the total number of species closer to 12 [7, 8]. Despite this reduction in the number of avian Trypanosoma spp. they are still a polyphyletic group .
Investigations into the trypanosomes of Australian wildlife in the past have demonstrated high levels of genetic and morphological diversity, mixed infections, and a lack of species specificity . In Australia, trypanosomes have been described from a variety of wild birds  and while there are six Trypanosoma spp. that have been described in Australian birds since 1910 [10–13] there is a need for taxonomic redescription to ensure current described species are confirmed/correlated with molecular sequence data [6, 9]. Trypanosoma sp. AAT was the first trypanosome isolated in vitro from an Australian bird, the currawong (Strepera sp.) that was also characterised using molecular techniques . Trypanosoma sp. AAT has been utilised in a number of genetic investigations representing an Australian trypanosome [14, 15]. The morphological information provided on Trypanosoma sp. AAT were two images of epimastigotes exhibiting long flagella and molecular sequences from the small ribosomal subunit 18S (18S rDNA) and glyceraldehyde 3-phosphate dehydrogenase (GAPDH) gene regions. A subsequent study in Australia that described Trypanosoma thomasbancrofti from the regent honeyeater (Anthochaera phrygia) and isolated T. avium from noisy minor birds (Manorina melanocephala) also provided sequences from the 18S rDNA and GAPDH gene regions .
The class Kinetoplastida, which contains all trypanosomes has a unique organelle called the kinetoplast containing extra-nuclear DNA (kDNA). The kDNA is contained inside the kinetoplast pocket that is part of the single large mitochondrion [16, 17], which is unusual in both its structural and functional properties [18, 19]. The structure and size of Trypanosoma mitochondria are variable and cell cycle dependant. This may be due to available carbon sources used in metabolism, especially high levels of glucose as this facilitates the transition from oxidative phosphorylation to glycolysis and reduces the size of the mitochondrion [20–22]. Additionally, kinetoplastids have a higher percentage of their DNA in their mitochondrion compared to other eukaryotes . For example, Trypanosoma cruzi the causative agent of Chagas disease can have up to 30% of its DNA in the kinetoplast-mitochondrion . The kDNA is made up of circular maxicircles and minicircles that appear as a network inside the kinetoplast pocket, which is attached to the flagellum by the tripartite attachment complex (TAC) . Maxicircles that encode for mRNA’s require RNA editing (post-transcriptional process of uridine insertion or deletion), which is achieved through guide RNA’s that are encoded on the minicircles . Minicircle size and kDNA width have been used in the past to differentiate between trypanosomes isolated from birds . The kDNA minicircles contain the ‘universal minicircle sequence’ (UMS or CSB-3), a 12- mer sequence (5'-GGGGTTGGTGTA-3'), which is conserved in most trypanosomatids although, the location and number of times it is present within the minicircles differ between species . In addition to this there are two other conserved sequence blocks within the minicircles (CSB-1, CSB-2). The UMS is the specific binding site for the UMS-binding protein (UMSBP), which is involved in kDNA replication  and anti UMSBP from Crithidia fasciculata has been used to detect homologous proteins in other trypanosomatids such as T. cruzi, Leishmania donovani and T. brucei [28–30]. Some trypanosomes isolated from birds such as T. avium possess what appears to be a unique kinetoplast, with unusually large minicircles [26, 31, 32] that make them intrinsically important tool in trying to understand kinetoplastid evolution and biology. As a result of the pleomorphism of avian trypanosomes within species, it has been suggested that in vitro investigations may be more reliable when trying to characterise their structure and understand the differences between species as in vitro studies provide a more stable environment [6, 33].
When investigating trypanosomes using current microscopy techniques there are a number of difficulties associated with interpreting 2-dimensional images in relation to the 3-dimensional (3D) organism. This is especially apparent in transmission electron microscopy (TEM), which allows for high resolution ultrastructural analysis in cells, but the sample sections only represent a small ~100 nm-thick segment of the cell. With this, the angle the section has been cut through a structure is usually not known making feature identification and accurate quantifiable measurements, at times difficult. The recent improvement in automated, high-throughput imaging techniques capable of high resolution 3D imaging overcomes these issues, and has led to 3D cellular architecture being characterised in Trypanosoma brucei [17, 34–36], T. cruzi [37, 38] and T. dionisii . A variety of morphological forms have been studied using a variety of different techniques that are available, including super resolution confocal microscopy , electron tomography [34, 37], serial block-face scanning electron microscopy [17, 36, 40], and focussed ion beam milling combined with scanning electron microscopy (FIB-SEM) [34, 38]. The primary difference between the latter two SEM-based techniques is that the serial block face method uses a knife to cut through the sample slice by slice permitting analysis areas in the order of hundreds of microns, while the FIB-SEM uses a beam of ions to cut through the sample permitting analyses on the scale of tens of microns.
The trypanosomes infecting birds must be better studied in order to understand trypanosome evolution, diversity, and structural biology. Therefore, the aim of this study was to resolve the taxonomy of Australian bird trypanosomes using molecular techniques, including, for the first time, a number of bird species from Western Australia. Additionally, an ultrastructural analysis of Trypanosoma sp. AAT was undertaken in order to better understand structural characteristics of an Australian avian trypanosome.
Collection of birds, 18S rDNA amplification, and sequencing of bird tissues
Specimens were collected opportunistically from dead birds handed into Murdoch University between 2008 and 2014 (sources included roadkill and fauna rehabilitation hospitals). Thirty Australian ravens (Corvus coronoides) and 13 Australian magpies (Cracticus tibicen) were included in the study along with a number of bird species residing in Australia (Additional file 1: Table S1). Birds were frozen at -20 °C following collection and dissected between March and December 2015. Dissected tissues were stored in 70% ethanol taking precautions to prevent cross-contamination between tissues. Up to seven tissues were extracted from 49 birds (n = 334) and up to three tissues extracted from 44 birds (n = 95) (Additional file 1). Genomic DNA was extracted using Quiagen Blood and Tissue Mini-kit (Quigen, Hilden, Germany) following the manufacturer’s protocols for tissue extraction including both positive and negative controls. All amplification reactions were performed in a PT100 thermocycler (MJ-Research). Trypanosome DNA was amplified using generic 18S rDNA PCR primers (SLF, S762R, S823F and S662R) in a nested PCR protocol [41, 42], under the following conditions: denaturation step at 94 °C for 5 min, followed by 35 cycles of 30 s at 94 °C, 30 s at 52 °C, 50 s at 72 °C, and a final extension step at 72 °C for 7 min. Both external and internal reactions contained 25 μl consisting of 1 μl of DNA, 0.8 μM of each primer, 0.2 mM of dNTPs, 2 mM of MgCl2 and 0.2 μl of Taq DNA polymerase for the external reaction. The internal reaction contained 1 μl of DNA, 0.8 μM of each primer, 0.2 mM of dNTPs, 1.5 mM of MgCl2 and 0.2 μl of Taq DNA polymerase. Due to the amplification of bird DNA by these primers tissues were also screened for trypanosomes using a subsequent nested primer set described in Noyes et al.  including external (TRY927F, TRY927R), and internal (SSU561F, SSU561R) primers under the following conditions: denaturation step at 94 °C for 5 min, followed by 30 cycles of 30 s at 94 °C, 1 min at 55 °C, 1 min and 30 s at 72 °C, and a final extension step at 72 °C for 10 min. Both external and internal reactions contained 25 μl consisting of 2 μl of DNA, 0.2 μM of each primer, 0.32 mM of dNTPs, 3 mM of MgCl2 and 0.2 μl of Taq DNA polymerase. PCR products were purified by cutting DNA bands using gel cutting tips from 2% agarose gel and using the freeze-squeeze method . Samples were sequenced in both directions using an ABI Prism™ Terminator Cycle Sequencing Kit on an Applied Bio-system 3730 DNA Analyser (Applied Bio-systems, California, USA). Sequences were edited and aligned using Geneious 8.1 .
A multiple-sequence alignment containing the 26 sequences isolated in this study from Western Australian birds, 47 sequences from trypanosome isolates downloaded from GenBank including two outgroups (T. brucei) was conducted using the MUSCLE  plugin for Geneious v. 8.1 . A GTR + G + I substitution model selected by jModelTest  was used in the construction of maximum-likelihood, neighbour-joining, and Bayesian analysis trees. Bootstrap support for 1000 replicates was performed for maximum-likelihood and neighbour-joining tree searches using MEGA 6 . A Bayesian analysis (10,000,000 generations, sampling frequency of 1000, ‘burn-in’ 3000) was run in Mr Bayes v. 3.1.2  plugin for Geneious v. 8.1. The final tree was edited using Inkscape.
Maintenance of trypanosomes in culture
Two vials of Trypanosoma sp. AAT originally isolated in 2004  were donated by Dr J. R. Stevens from Bristol University, UK and were identified using generic trypanosome primers described in section 2.1 [41, 42]. Trypanosomes were grown in an incubator at 28 °C with 5% CO2. Cultures were maintained in biphasic medium containing Brain-heart infusion (BHI), BBL agar- grade A, 0.48% gentamicin, and 10% defibrinated rabbit blood as a solid phase, and either RPMI 1640 (Roswell Park Memorial Institute 1640) supplemented with tryptose (TRPMI) as in Noyes et al. , or Grace’s insect media  as a liquid phase. All liquid media was supplemented with 10% heat-inactivated foetal calf serum (FCS) and 1% penicillin-streptomycin.
Scanning and transmission electron microscopy
For scanning electron microscopy (SEM), trypanosomes were fixed in 2.5% glutaraldehyde in 1× PBS and stored at 4 °C before being mounted on poly-L-lysine coated coverslips, dehydrated through a series of ethanol solutions (30%, 50%, 70%, 90%, 100%, 100%) using a PELCO Biowave then processed in a critical point drier. Coverslips were mounted on stubs with adhesive carbon, coated with 2 nm platinum (Pt) and 10 nm carbon. Trypanosomes were imaged at 3 kV using the in-lens secondary electron detector on a Zeiss 55VP field emission SEM. For transmission electron microscopy (TEM) trypanosomes were fixed in 2.5% glutaraldehyde in 1× PBS and processed using a PELCO Biowave microwave, where samples were post-fixed in 1% OsO4 in 1× PBS followed by progressive dehydration in ethanol (30%, 50%, 70%, 90%, 100%) then acetone, before being infiltrated and embedded overnight at 70 °C in epoxy resin Procure-Araldite. Sections ~120 nm-thick were cut with a diamond knife on a Leica microtome and mounted on copper grids. Digital images were collected from unstained sections at 120 kV on a JEOL 2100 TEM fitted with a Gatan ORIUS1000 camera.
Focused ion beam - scanning electron microscopy
Trypanosoma sp. AAT samples were fixed in 2.5% glutaraldehyde in 1× PBS and stored at 4 °C before heavy metal staining, which had been adapted from previous methods [40, 51]. Samples were washed in 1× PBS three times then processed through 2% osmium tetroxide + 1.5% potassium ferricyanide for 1 h, thiocarbohydrazide for 20 min, 2% osmium tetroxide for 30 min, and finally left in 1% aqueous uranyl acetate overnight at 4 °C. The following day samples were stained with lead aspartate (20 mM lead nitrate in 0.03 M L-aspartic acid adjusted to pH 5.5 with 1 M KOH) for 1 h . Samples were washed with water thoroughly between each stain three times for a duration of 5 min. Following staining, samples were dehydrated through a series of ethanol (20%, 50%, 70%, 90%, 100%, 100%) followed by acetone, and infiltrated using Hard plus resin 812 (25%, 50%, 75%, 100%) . Samples were embedded in fresh 100% resin before being cured at 70 °C for 48 h. Samples were trimmed using a glass knife on a Leica microtome to locate sites of interest, attached to a 45 degree-angled metal stub using aluminium tape, coated with 10 nm Pt, and prepared and imaged in a FEI Helios G3 FIB-SEM. To prepare sites of interest, a protective coating of 1 μm Pt was deposited on the top surface of the region of interest (ROI) and side trenches (~15 μm3) were dug either side. The face of the ROI was then progressively milled and imaged in 25 nm steps. Milling was performed at 7 degrees (=52 degree actual tilt) and a working distance of ~4 mm using a Ga beam at 0.79 nA and 30 kV. Back scattered electron images were collected after each milling step at 45 degrees (=0 degree actual tilt) and a 2 mm working distance using a through lens electron detector (TLD) at 2 kV and 0.69 nA beam current. 3D data were aligned and processed using Amira 6.0 for FEI systems.
UMS amplification and sequencing
A fragment of Trypanosoma sp. AAT minicircles was amplified by PCR using the UMS as a forward primer (UMSF 5'-GGG GTT GGT GTA-3'), and its complementary sequence as a reverse primer (UMSR 5'-TAC ACC AAC CCC-3') under the following conditions: an initial step of 95 °C for 5 min, followed by 35 cycles of 30 s at 95 °C, 30 s at 40 °C, and 60 s at 72 °C, and a final extension step of 5 min at 72 °C. Reactions contained 25 μl consisting of 1 μl of DNA, 1.5 mM of each primer, 200 mM of dNTPs, 0.2 μl of Taq DNA polymerase, and 1.5 mM of MgCl2. DNA was purified using an Agencourt AMPure PCR Purification system (manufacturer’s instructions). Purified amplicons were sequenced using an ABI Prism™ Terminator Cycle Sequencing kit (Applied Bio-systems, California, Foster City, USA) on an Applied Bio-system 3730 DNA Analyzer. Sequences were aligned with the minicircles of T. rangeli (accession number L19395T), T. lewisi (accession number M17995), two strains of T. cruzi (accession numbers X04680, M18814), and two strains of T. copemani (accession numbers TBA) using MUSCLE .
Total protein extract from Trypanosoma sp. AAT epimastigotes was obtained by centrifugation of 1 × 106 epimastigotes at 8000 × g for 5 min. The pellet was washed, centrifuged twice in 1× PBS, and resuspended in 40 μl of water. Subsequently, 10 μl of 10% SDS (Sodium Dodecyl Sulfate) was added and samples were sonicated for 5 min. After sonication, cell lysates were solubilised in cracking buffer containing final concentrations of 50 mM Tris-HCl, pH 6.8, 4% SDS (wt/vol), 3.5% (vol/vol) beta-mercaptoethanol, 10% (vol/vol) glycerol, and 10 mM EDTA. The solution was centrifuged at 10,000 × g for 30 min at 4 °C. The protein concentration was determined using the direct-detect assay free-cards (EMD millipore corporation, Billerica, USA). Protein extract (30 μg) was boiled at 70 °C for 10 min and loaded onto a NuPag10 4-12% Bis-Tris gel. Protein bands on the gel were transferred onto a nitrocellulose membrane using the turbo-transfer system (Biorad, Hercules, USA). The membrane was blocked by incubation in 5% skim dry milk -diluted in TBST (tris-buffer solution tween) for 2 h with constant shaking, and probed with a 1:4000 dilution of Crithidia fasciculata anti-UMSBP overnight at 4 °C. The membrane was then washed three times with TBST and then incubated with a 1:10,000 dilution of ECL peroxidase labelled conjugated anti-rabbit secondary antibody (Jackson ImmunoResearch Laboratories, Inc. West Grove, USA) for 2 h followed by ECL detection as recommended by the manufacturer (Amersham Pharmacia Biotech, Piscataway, USA).
Bird tissues screened for Trypanosoma spp.
Bird tissues that tested positive for Trypanosoma spp. Bird identification number (ID), bird species, tissue, and Trypanosoma spp. are included. Tissues extracted include striated or skeletal muscle (Sm), heart (H), liver (L), spleen (S), lung (Ln), thoracic muscle (T) and brain (B)
Boobook (Ninox novaeseelandiae)
Trypanosoma sp. CC2016 B002
Ln, B, K
Currawonga (Strepera spp.)
Trypanosoma sp. AAT
Falcon (Falco spp.)
Barn owl (Tyto alba)
Australian dovea (Family Columbidae)
Australian magpiea (Cracticus tibicen)
Singing honeyeatera (Gavicalis virescens)
Australian magpie (Cracticus tibicen)
Silvereye (Zosterops lateralis)
Australian mudlark (Grallina cyanoleuca)
Trypanosoma sp. C-111 
Pink and grey galah (Eolophus roseicapilla)
Trypanosoma sp. AAT
Pigeon (Columba livia)
Australian raven (Corvus coronoides)
Australian raven (Corvus coronoides)
Sm, B, T
Australian raven (Corvus coronoides)
Trypanosoma sp. CC2016 B069
Australian magpie (Cracticus tibicen)
Trypanosoma sp. AAT
Australian magpie (Cracticus tibicen)
Trypanosoma sp. AAT
Silver gull (Chroicocephalus novaehollandiae)
Trypanosoma sp. AAT
Ultrastructural analysis of Trypanosoma sp. AAT
Additional file 2: High resolution 3D electron microscopy volume rendering of Trypanosoma sp. AAT small epimastigote. Images for the video were acquired using FIB-SEM, including individual sections, and segmented organelles; kinetoplast (red), nucleus (blue) and mitochondrion (pink). (MPG 48,541 kb)
The universal minicircle sequence and binding protein in Trypanosoma sp. AAT
Trypanosoma sp. AAT kinetoplast minicircle conserved sequence blocks CSB-1, CSB-2, and CSB-3 (UMS). Trypanosoma sp. AAT and other Trypanosoma spp. are shown. Differences are shown in bold
CSB-3 or UMS
Barrois et al 
T. cruzi Y strain
González et al. 
T. copemani G1
Botero et al. 
T. copemani G2
Botero et al. 
Trypanosoma sp. AAT
Cross-continental avian Trypanosoma spp.
Microscopy or culture of tissues from birds in the past did not yield any positive trypanosome identification , but in the present study many tissues tested positive by PCR. This demonstrates that tissues can be a valid tool for identifying Trypanosoma spp. infection. Trypanosoma spp. in Western Australia are diverse, cross-continental in distribution, and non-species specific, which is consistent with recent studies of avian trypanosomes elsewhere [8, 13, 26, 60]. Four Trypanosoma spp. isolated in Western Australia including T. avium, T. thomasbancrofti, T. culicavium, and an unknown Trypanosoma spp. (group C-111 in Zidková et al. ) have an intercontinental distribution. Of these, T. avium was the most common trypanosome found in eight of 18 infected birds. The most recently described avian Trypanosoma spp. is T. thomasbancrofti that was found in regent honeyeaters, and now in a boobook, Australian magpie, and a falcon. Before its formal description T. thomasbancrofti was found in a number of birds in Europe . This is the first report of T. culicavium in Australia, which was identified in Culex mosquitos and the collared flycatcher (Ficedula albicollis) in central Europe . A currently unnamed isolate from the group designated Trypanosoma spp.  and group C-III (Zidková et al. ) identified in birds and mosquitoes in central Europe was found for the first time in Australia, in an Australian mudlark. While most of the Australian birds infected with these Trypanosoma spp. are non-migratory outside Australia they often have wide distributions across Australia and into numerous pacific islands. However, the bird species infected with the Trypanosoma spp. identified are not closely related. For example, T. avium was found in seven different avian species that belong in four different orders including; Passeriformes (Australian magpie and raven), Strigiformes (boobook and barn owl), Falconiformes (falcon), and Columbiformes (pigeon, Australian dove), which raises questions about why avian trypanosome species are so conserved. A possible reason for the relatively conserved number of avian trypanosomes include a high level of vectorial specificity, thus involving invertebrate species that are very common and occur on all continents. However, at this stage little is known of the vectors in Australia [9, 61], while avian trypanosome vectors are considered to be biting flies or mosquitos elsewhere in the world [26, 33]. In Australia, leeches , biting flies , and ticks  have been suggested most frequently in the literature as vector candidates for avian trypanosomes.
Australian avian Trypanosoma isolates
One novel isolate was identified in the study (Trypanosoma sp. CC2016 B002) from a boobook, which is a native owl widely distributed across Australia and a number of pacific islands. However, only a partial region of nuclear DNA was sequenced from a single sample, which is insufficient to characterise a new species. Trypanosoma sp. CC2016 B002 was positioned between T. bennetti and T. culicavium in phylogenetic analysis. A subsequent isolate found only in Australia is Trypanosoma sp. AAT, which was identified in a currawong as well as two Australian magpies, a silver gull (Chroicocephalus novaehollandiae), and a pink and grey galah (Eolophus roseicapilla). These birds are all native to Australia and occasionally migrate within its borders depending on temperature or food source availability  explaining the presence of Trypanosoma sp. AAT on both west (this study) and east  coasts of Australia. While Trypanosoma sp. AAT has only been found in Australia, it is closely related to T. corvi in both nuclear and mitochondrial gene regions , and genotypes from the T. corvi species clade have been identified in numerous bird species worldwide . Of the common bird trypanosomes found worldwide the species not identified in the current study were T. bennetti and T. corvi, which is interesting as it has been suggested that most avian trypanosomes fall into one of three species, T.avium, T. corvi or T. bennetti . The close genetic relationship observed between Trypanosoma sp. CC2016 B002/T. thomasbancrofti and Trypanosoma sp. AAT/T. corvi suggest larger studies incorporating more bird species and larger sample sizes may identify additional novel isolates, including those of T. bennetti and T. corvi.
Another trypanosome found in an avian host for the first time was Trypanosoma sp. CC2016 B069 isolated from an Australian raven. Trypanosoma sp. CC2016 B069 was highly similar to Trypanosoma sp. TL.AQ.22 in phylogenetic analysis and the region of 18S rDNA that was amplified in this study differing at 10 sites in a 494 bp fragment. Trypanosoma sp. TL.AQ.22 was previously reported from an Australian haemadipsid leech and placed in the Trypanosoma theileri clade . The original study that isolated Trypanosoma sp. TL.AQ.22 found it was similar to Trypanosoma cyclops isolated from a monkey in Asia, Trypanosoma sp. ABF found in a wallaby, and a number of other isolates from terrestrial leaches . This led the researchers to conclude leeches from the family Haemadipsidae could be important vectors in Australia and Asia. The present study is not the first to identify similar trypanosomes infecting a mammal and a bird. A partial sequence of Trypanosoma 18S rDNA that was obtained from a boodie (Bettongia lesueur) was identical to the avian Trypanosoma sp. AAT . Both these organisms could be transmitted by the same vector, supporting the proposal that bird trypanosomes are similar due to high specificity towards the vector. However, birds and mammals being infected with the same trypanosome species is contradictory to the specificity of avian trypanosomes observed across continents. It is difficult to understand the path of transmission when so little is known about the life-cycles, vectors, and biology of avian and Australian Trypanosma spp.
Trypanosoma sp. AAT ultrastructure
The majority of investigations into avian trypanosomes have involved analysis of trypomastigotes present in blood. Here, however the epimastigote stage was investigated because it is the morphological form that is grown in vitro and it has become increasingly clear that this is a more appropriate way to investigate their biology [6, 9]. With this, there are few Trypanosoma spp. to compare with the epimastigote biology of Trypanosoma sp. AAT. Despite their close genetic relationship and similar kinetoplast width, the description of Trypanosoma sp. AAT in vitro otherwise differs considerably when compared to the morphology of the closely related T. corvi. Three morphotypes were observed of Trypanosoma sp. AAT and both epimastigote forms were significantly larger than T. corvi epimastigotes [7, 33]. T. corvi had one epimastigote (19 ± 2 μm) when grown in culture , while a description from bone marrow identified a number of morphotypes including epimastigotes (shorter than 20 μm) with tapered ends, and trypomastigotes . Trypanosoma sp. AAT kDNA appear most similar to T. corvi and T. culicavium, and were less similar to those of T. avium or T. thomasbancrofti, which are much stouter in TEM micrographs [13, 26, 33]. The kDNA width of Trypanosoma sp. AAT (kDNA width = 0.39 μm) did not differ from T. corvi (kDNA width = 0.39 μm), but was significantly different to T. culicavium (kDNA width = 0.31 μm) [26, 33]. However, there is considerable variation in kDNA width between individuals even when measuring them using volume analysis, which is more accurate than measuring cross-sections used for TEM analysis. The variation is present even though only 1K1N trypanosomes were counted in the analysis, which implies there is some variation in the size of the kinetoplast within the epimastigote stage. Trypanosoma sp. AAT is most likely a separate species from T. corvi based on morphology as well as differences in 18S rDNA and GAPDH gene regions that were observed . Although, the limited structural and molecular information available on avian trypanosomes combined with a high level of diversity within apparent species groups has resulted in unclear species boundaries between isolates. At this stage more information on avian trypanosomes is required before Trypanosoma sp. AAT can be conclusively placed within T. corvi or characterised as a new species.
The first comprehensive high-resolution, 3-dimensional, ultrastructural study of Trypanosoma sp. AAT revealed that the kinetoplast is disc-shaped and perpendicular to the rest of the mitochondrion. The mitochondrion was observed under the subpellicular microtubules in the smaller epimastigotes and is a vast branching structure occupying a large volume in the cytoplasm. In T. cruzi and T. dionisii 3D reconstructions, the epimastigote mitochondrion is extensive and positioned in the same place as Trypanosoma sp. AAT - just under the subpellicular microtubules -, the kinetoplast pocket is positioned underneath the nucleus not alongside it [39, 65]. In T. cruzi amastigotes 3D reconstructions revealed the mitochondrion has a horse shoe shape [18, 66] while T. brucei trypomastigotes in the vertebrate host have a poorly developed branching mitochondrion [17, 35, 36]. Direct glycolysis may be used in the presence of high glucose concentrations (such as the blood) reducing the size of the mitochondrion between morphological forms and increasing the size of the glycosomes, which was observed in Herpetomonas roitmani  and T. brucei [20, 21] suggesting the parasites switch from oxidative phosphorylation to glycolysis. This process may reverse in the presence of low glucose environments such as the invertebrate gut resulting in a larger mitochondrion [22, 68]. A smaller reduced mitochondrion was observed in the larger epimastigotes compared to the smaller epimastigotes grown in the same medium and harvested at the same time in this study. Therefore, differences in size between epimastigote forms was not solely due to nutrient availability, but could be cell-cycle dependent or due to differences in how various morphological forms metabolise and develop. Epimastigotes occur in the bone marrow of birds  as well as the invertebrate vector, while the blood contains trypomastigotes as in other Trypanosoma spp. [33, 69]. This is interesting as it could be hypothesised that the larger Trypanosoma sp. AAT epimastigote is likely to occur in bone marrow where there is a high glucose content and the smaller epimastigote in the insect vector that is likely more reliant on L-proline for a carbon source . The size and shape of the reservosomes, glycosomes, and acidocalcisomes also differs between the two sizes of epimastigotes observed in Trypanosoma sp. AAT that is both cell cycle and nutrient dependent in other trypanosomes, especially T. brucei, which has been extensively studied [18, 19, 56, 68]. Put simply, due to the similarity in nutrient availability for the two epimastigotes observed in this study, differences in organelle structure is most likely cell-cycle dependent.
Parasitism is likely to have emerged in trypanosomatids due to this group of organisms containing both free-living and obligate parasites, and the shape and structure of the kinetoplast is important in understanding the evolution of trypanosomes [70, 71]. The kDNA is simply dispersed throughout the mitochondrial matrix in early trypanosomatids such as bodonids, while in avian trypanosomes the minicircles are larger than that of the later branching trypanosomes including T. brucei and T. cruzi . Two of the three minicircle sequence blocks common amongst late branching trypanosomes like T. cruzi (CSB-1 and CSB-2) are quite different compared to those of Trypanosoma sp. AAT. Avian trypanosomes have larger minicircles compared to other trypanosomes, so the differences in these regions are not unexpected . However, there are aspects of kDNA that are highly conserved. The 12-mer UMS (or CSB-3), which is present in the minicircles of all trypanosomatids investigated , was found in Trypanosoma sp. AAT. The UMS binding protein that is involved in kDNA replication, which is found in other kinetoplastids such as C. fasciculata, T. cruzi, L. donovani and T. brucei [28–30, 72], was also present in Trypanosoma sp. AAT. Although, results suggested Trypanosoma sp. AAT contains three different UMSBPs. Interestingly, the size of two Trypanosoma sp. AAT UMSBPs (16.4 and 25.7 kD) was exactly the same as the UMSBPs found on the minicircles of the Australian marsupial trypanosome T. copemani .
The molecular and structural information provided in this study contribute to understanding the diversity and structural biology of avian trypanosomes. While it is clear avian trypanosomes are cross-continental and exist in fewer species groups than are currently described, further studies incorporating molecular and structural techniques are required to establish the true extent of bird trypanosome diversity. Despite the close relationship with T. corvi, Trypanosoma sp. AAT is most likely a separate species currently found only in Australia. However, more information is required on avian trypanosomes in general, in order to provide clearer species boundaries. The first 3-dimentional ultrastructural analysis of an avian trypanosome provides interesting information on their morphology and organelle arrangement. Although, a greater understanding of avian trypanosome ultrastructure and metabolism, would assist in understanding their life-cycles and the impact of infection on their hosts. The possibility that avian Trypanosoma spp. are also infecting mammals and could be transmitted by haemadipsid leeches should be further investigated. Additional research on the trypanosomes infecting birds and their vectors will hopefully explain why so many avian trypanosomes are cross-continental but not species-specific.
The authors thank Rick Webb at University of Queensland and Minh Huynh at University of Sydney for advice regarding heavy metal staining protocols, and Frances Brigg at the Western Australian State Agricultural Biotechnology Centre, Murdoch University for operating the bioanalyser. Thanks are extended to professor Joseph Shlomai from the Department of Microbiology and Molecular Genetics at The Hebrew University- Hadassah Medical School for providing Crithidia fasciculata anti-UMSBP and recombinant UMSBP. The authors also thank Associate Professor Martin Saunders, Dr Jeremy Shaw, and Dr Andrew Mehnert for support in relation to FIB-SEM data acquisition and analysis, and acknowledge use of the facilities of the Australian Microscopy and Microanalysis Research Facility at the Centre for Microscopy, Characterisation & Analysis (CMCA), the University of Western Australia, a facility funded by the University, State and Commonwealth Governments.
This research was supported with funding from the Western Australian Government’s State NRM Program.
Availability of data and material
The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request, where not included in the published article or additional files.
CC wrote the article. AK and AT dissected the birds. CC and AK performed DNA extractions. CC performed PCRs, sequencing, and phylogenetic analysis. AB carried out the UMS / UMS-BP experiments and analysis. CC grew the parasites, fixed all samples, and conducted all microscopy (with substantial help from PC with FIB-SEM experiments), and Amira analysis. All authors edited and commented on the article. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
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Animal tissues were collected opportunistically from dead birds and ethics approval was not required.
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