IE20090467U1 - Ace2 as a target gene for the molecular identification of yeast and fungal species. - Google Patents

Abstract

ABSTRACT the present invention relates to nucleic acid primers and probes for use in the idcntilictition of one or more yeast species. More specifically the invention relates to the Ace) gene. the corresponding RNA. specific probes, primers and oligonueleotides related thereto and their use in diagnostic assays to detect and I or discriminate between yeast species.

Description

Field of the Invention The present invention relates to nucleic acid primers and probes for use in the identification of one or more yeast species. More specifically the invention relates to the Ace2 gene, the corresponding RNA, specific probes, primers and oligonucleotides related thereto and their use in diagnostic assays to detect and I or discriminate between yeast species.

Background to the_lnr\'ention I0 Yeast and fungal infections represent a major cause of morbidity and mortality among immunocompromised patients. The number of immunocompromised patients at risk of yeast and fungal infection continues to increase each year, as does the spectrum of fungal and yeast agents causing disease. Mortality from fungal infections, particularly invasive fungal infections, is 30% or greater in certain risk groups. The array of IS available anti-fungal agents is growing; however, so too is the recognition of both intrinsic and emerging resistance to antifungal drugs. These factors are contributing to the increased need for cost containment in laboratory testing and have led to laboratory consolidation in testing procedures.

Invasive fiingal infections are on the increase. In 2003, it was estimated that there were 9 million at risk patients of which l.2 million developed infection. Candida species now rank as the most prominent pathogens infecting immunosupressed patients. In particular, infections are common in the urinary tract, the respiratory system and the bloodstream. at the site of insertion of stents, catheters and orthopaedic joints.

Approximately 10% of the known Candida spp. have been implicated in human infection. Invasive candidiasis occurs when candida enters the bloodstream and it is estimated to occur at a frequency of 8/ 1 00,000 population in the US with a mortality rate of 40%. Candida albicans is the 4"‘ most common cause of bloodstream infection.

Emerging mycoses agents include F usarium, Scedosporium, Zygomycetes and 'l‘richosporon spp. (“Stakeholder Insight; Invasive fungal infections", Daramonitor, Jan lmmunocompromised patients including transplant and surgical patients, fungal infections, options outweigh replacements 2004). A large number of severe cases of sepsis are reported each year. Despite improvements in its medical management, sepsis still constitutes one of the greatest challenges in intensive care medicine. Microorganisms (bacteria, fungi and yeast) responsible for causing sepsis are traditionally detected in hospital laboratories with the aid ofmicrobiological culture methods with poor sensitivity (25-82%), which are very time-consuming, generally taking from two to five days to complete. and up to eight days for the diagnosis of fungal infections.

Definitive diagnosis of infection caused by yeast or fungus is usually based on either, the recovery and identification of a specific agent from clinical specimens or microscopic demonstration of fungi or yeasts with distinct morphological features.

However, there are numerous cases where these methods fail to provide conclusive proof as to the infecting agent. In these instances, the detection of specific host antibody responses can be used, although again this can be affected by the immune status of the patient. Time is critical in the detection and identification of bloodstream infections typically caused by bacteria, yeast or fungi. Effective treatment depends on finding the source of infection and making appropriate decisions about antibiotics or antifungals quickly and efficiently.

Fungal and yeast nucleic acid based diagnostics have focused heavily on the ribosomal RNA (rRNA) genes, RNA transcripts, and their associated DNA / RNA regions. The rRNA genes are highly conserved in all fungal species and they also contain divergent and distinctive intergenic transcribed spacer regions. Ribosomal rRNA comprises three genes: the large sub-unit gene (288), the small sub-unit gene (I SS) and the 5.8S gene. The 288 and 18S rRNA genes are separated by the 5.88 rRNA and two internal transcribed spacers (ITSI and ITS2). Because the ITS region contains a high number of sequence polymorphisms, numerous researchers have concentrated their efforts on these as targets (Atkins and Clark, 2004). rRNA genes are also multicopy genes with >10 copies within the fungal genome.

A number of groups are working on developing new assays for fungal and yeast infections. US2004044193 relates to, amongst a number of other aspects, the transcription factor CaTECl of Candida albicans; inhibitors thereof, and methods for the diagnosis and therapy of diseases which are connected with a Candida infection; and also diagnostic and pharmaceutical compositions which contain the nucleotide sequences, proteins, host cells and/or antibodies. WO0183824 relates to hybridization lE090467 assay probes and accessory oligonucleotides for detecting ribosomal nucleic acids from Candida albicans and/or Candida dubliniensis. US60l7699 and US5426026 relate to a set of DNA primers, which can be used to amplify and speciate DNA from five medically important Candida species. US 6747137 discloses sequences useful for diagnosis of Candida infections. EP 0422872 and US 5653726 disclose probes based on 18S rRNA genes, and US 5958693 discloses probes based on 28S rRNA, for diagnosis of a range of yeast and fungal species. US 6017366 describes sequences based on chitin synthase gene for use in nucleic acid based diagnostics for a range of Candida species.

It is clear though, that development of faster, more accurate diagnostic methods are required, particularly in light of the selection pressure caused by modern anti- microbial treatments which give rise to increased populations of resistant virulent strains with mutated genome sequences. Methods that enable early diagnosis of microbial causes of infection enable the selection of a specific narrow spectrum antibiotic or antilungal to treat the infection (Datamonitor report: Stakeholder opinion —lnvasive lungal infections, options outweigh replacements 2004; Datamonitor report: Stakeholder Opinion-Sepsis, under reaction to an overreaction, 2006).

Only after pathogens are correctly identified can targeted therapy using a specific antibiotic or antifungal begin. Many physicians would like to see the development of better in vitro amplification and direct detection diagnostic techniques for the early diagnosis of yeast and fimgi (“Stakeholder Insight: Invasive fungal infections”, Datamonitor, Jan 2004). The present invention provides novel fungal and yeast nucleic acid targets for application in Nucleic Acid Diagnostics (NAD) tests.

These are rapid, accurate diagnostic tests for clinically significant bacterial and fungal pathogens for bioanalysis applications in the clinical sector.

Ace2 is a DNA-binding cell cycle regulated transcription factor. Ace2 functions similarly to the transcription factor SW15, yet they activate distinct genes. The translated Ace2 protein is present in the nucleus in early G1 phase of the cell cycle and thus, specifically activates the expression of genes in the G1 phase. In particular, it activates the CTS1 gene. CTS1 is a chitinase-encoding gene required to degrade the cell wall between parent and daughter cells during cytokinesis. There are 7 Ace2 sequences publicly available in the NCBI GenBank database including 5 Candida Spp. sequences. There are no published Ace2 sequences available for Aspergillus spp. The current inventors have designed PCR primers to amplify the region of Ace2 in Candida lE090467 4 spp. equivalent to base pair position 1736 to 2197 in C. albicans. This region of the Acc2 gene has an application for the molecular identification and / or discrimination of yeast species.

Definitions “Synthetic oligonucleotide" refers to molecules of nucleic acid polymers of 2 or more nucleotide bases that are not derived directly from genomic DNA or live organisms. The term synthetic oligonucleotide is intended to encompass DNA, RNA, and DNA/RNA hybrid molecules that have been manufactured chemically, or synthesized enzymatically in vitro.

An "oligonucleotide" is a nucleotide polymer having two or more nucleotide subunits covalently joined together. Oligonucleotides are generally about 10 to about 100 nucleotides. The sugar groups of the nucleotide subunits may be ribose, deoxyribose, or modified derivatives thereof such as OMe. The nucleotide subunits may bcjoined by linkages such as phosphodiester linkages, modified linkages or by non- nucleotide moieties that do not prevent hybridization of the oligonucleotide to its complementary target nucleotide sequence. Modified linkages include those in which a standard phosphodiester linkage is replaced with a different linkage, such as a phosphorothioate linkage. a methylphosphonate linkage, or a neutral peptide linkage.

Nitrogenous base analogs also may be components ofoligonucleotides in accordance with the invention.

A "target nucleic acid" is a nucleic acid comprising a target nucleic acid sequence. A “target nucleic acid sequence," "target nucleotide sequence" or "target sequence“ is a specific deoxyribonucleotide or ribonucleotide sequence that can be hybridized to a complementary oligonucleotide.

An "oligonucleotide probe" is an oligonucleotide having a nucleotide sequence sufficiently complementary to its target nucleic acid sequence to be able to form a detectable hybrid probe:target duplex under high stringency hybridization conditions. An oligonucleotide probe is an isolated chemical species and may include additional nucleotides outside of the targeted region as long as such nucleotides do not prevent hybridization under high stringency hybridization conditions. Non- complementary sequences, such as promoter sequences, restriction endonuclease recognition sites, or sequences that confer a desired secondary or tertiary structure such as a catalytic active site can be used to facilitate detection using the invented probes. An lEca0467 oligonucleotide probe optionally may be labelled with a detectable moiety such as a radioisotope, a fluorescent moiety, a chemiluminescent, a nanoparticle moiety, an enzyme or a ligand, which can be used to detect or confirm probe hybridization to its target sequence. Oligonucleotide probes are preferred to be in the size range of from about 10 to about 100 nucleotides in length, although it is possible for probes to be as much as and above about 500 nucleotides in length, or below 10 nucleotides in length.

A "hybrid" or a "duplex" is a complex formed between two single-stranded nucleic acid sequences by Watson-Crick base pairings or non-canonical base pairings between the complementary bases. "Hybridization" is the process by which two complementary strands of nucleic acid combine to fonn a double-stranded structure ("hybrid" or "duplex"). A "fungus" or "yeast" is meant any organism of the kingdom Fungi, and preferably, is directed towards any organism of the phylum Ascomycola.

"Complementarity“ is a property conferred by the base sequence of a single strand of DNA or RNA which may fonn a hybrid or double-stranded I)N/\:[)N/\.

RNA:RNA or DNA:RNA through hydrogen bonding between Watson-C rick base pairs on the respective strands. Adenine (A) ordinarily complements thymine (T) or uracil (U), while guanine (G) ordinarily complements cytosine (C).

The term "stringency" is used to describe the temperature, ionic strength and solvent composition existing during hybridization and the subsequent processing steps.

Those skilled in the art will recognize that “stringency” conditions may be altered by varying those parameters either individually or together. Under high stringency conditions only highly complementary nucleic acid hybrids will form; hybrids without a sufficient degree of complementarity will not form. Accordingly, the stringency of the assay conditions determines the amount of complementarity needed between two nucleic acid strands forming a hybrid. Stringency conditions are chosen to maximize the difference in stability between the hybrid formed with the target and the non-target nucleic acid.

With “high stringency” conditions, nucleic acid base pairing will occur only between nucleic acid fragments that have a high frequency of complementary base sequences (for example, hybridization under “high stringency" conditions, may occur between homologs with about 85-100% identity, preferably about 70-100% identity).

With medium stringency conditions, nucleic acid base pairing will occur between nucleic acids with an intermediate frequency of complementary base sequences (for lEaso467 example, hybridization under “medium stringency” conditions may occur between homologs with about 50-70% identity). Thus, conditions of “weak” or “low" stringency are often required with nucleic acids that are derived from organisms that are genetically diverse, as the fiequency of complementary sequences is usually less.

‘High stringency’ conditions are those equivalent to binding or hybridization at 42° C. in a solution consisting of SXSSPE (43.3g/1 NaCl, 6.9 g/l N3H3PO4H2O and 1.35 g/l EDTA, ph adjusted to 7.4 with NaOH), 0.5% SDS, 5xDenhardt’s reagent and l00ug/ml denatured salmon sperm DNA followed by washing in a solution comprising 0.lxSSPE, l.0%SDS at 42° C. when a probe of about 500 nucleotides in length is used.

“Medium stringency’ conditions are those equivalent to binding or hybridization at 42° C. in a solution consisting of SXSSPE (43.8 g/l NaCl, 6.9 g/l NaH2PO.;I‘I;O and 1.85 g/l EDTA, pH adjusted to 7.4 with NaOH), 0.5% SDS, 5xDenhardt’s reagent and 100 pg/ml denatured salmon sperm DNA followed by washing in a solution comprising l.0xSSPl3, 1.0% SDS at 42° C, when a probe ofabout 500 nucleotides in length is used.

‘Low stringency’ conditions are those equivalent to binding or hybridization at 42° C. in a solution consisting of SXSSPE (43.8 g/l NaCl, 6.9 g/l NaH2P04H2O and 1.85 g/l EDTA, pH adjusted to 7.4 with NaOH), 0.1% SDS, 5xDenhardt’s reagent |50xDenhardt’s contains per 500ml: Sg F icoll (Type 400, Pharamcia), 5 g BSA (Fraction V; Sigmaj] and 100 pg/ml denatured salmon sperm DNA followed by washing in a solution comprising SXSSPE, 0.1% SDS at 42° C, when a probe of about 500 nucleotides in length is used.

In the context of nucleic acid in-vitro amplification based technologies, “stringency” is achieved by applying temperature conditions and ionic buffer conditions that are particular to that in-vitro amplification technology. For example, in the context of PC R and real-time PCR, “stringency” is achieved by applying specific temperatures and ionic buffer strength for hybridisation of the oligonucleotide primers and, with regards to real-time PCR hybridisation of the probe/s, to the target nucleic acid for in- vitro amplification of the target nucleic acid.

One skilled in the art will understand that substantially corresponding probes of the invention can vary from the referred-to sequence and still hybridize to the same target nucleic acid sequence. This variation from the nucleic acid may be stated in terms of a percentage of identical bases within the sequence or the percentage of perfectly IE09s467 complementary bases between the probe and its target sequence. Probes of the present invention substantially correspond to a nucleic acid sequence if these percentages are from about l00% to about 80% or from 0 base mismatches in about 10 nucleotide target sequence to about 2 bases mismatched in an about 10 nucleotide target sequence. In preferred embodiments, the percentage is from about 85% to about 100%. In more preferred embodiments, this percentage is from about 90% to about l00%; in other preferred embodiments, this percentage is from about 95% to about 100%, eg. 95%, 96%, 97%, 98%, 99%, or 100%.

By "sufficiently complementary" or "substantially complementary" is mcant nucleic acids having a sufficient amount of contiguous complementary nucleotides to form, under high stringency hybridization conditions. a hybrid that is stable for detection. Substantially complementary to can also refer to sequences with at least 9 % identity to, e.g., 95, 96, 97, 98, 99, or 100% identity to, a given reference sequence.

The terms “identical" or percent “identity,” in the context of two or more nucleic acids or polypeptide sequences, refer to two or more sequences or subsequences that are the same or have a specified percentage of amino acid residues or nucleotides that are the same (i.e., about 60% identity, preferably 65%, 70%, 75%. 80%, 85%, 90%, 91%, 92"/o, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or higher identity over a specified region, when compared and aligned for maximum correspondence over a comparison window or designated region) as measured using a BLAST or BLAST 2.0 sequence comparison algorithms with default parameters described below, or by manual alignment and visual inspection (see, e. g., NCBI web site at ncbi.n!m.nih.gov/BI.AST/ or the like). Such sequences are then said to be “substantially identical.” This definition also refers to, or may be applied to, the compliment of a test sequence. The definition also includes sequences that have deletions and/or additions, as well as those that have substitutions. As described below, the preferred algorithms can account for gaps and the like. Preferably, identity exists over a region that is at least about 25 amino acids or nucleotides in length, or more preferably over a region that is 50-100 amino acids or nucleotides in length.

For sequence comparison, typically one sequence acts as a reference sequence, to which test sequences are compared. When using a sequence comparison algorithm, test and reference sequences are entered into a computer, subsequence coordinates are lE090467 designated, if necessary, and sequence algorithm program parameters are designated.

Preferably, default program parameters can be used, or altemative parameters can be designated. The sequence comparison algorithm then calculates the percent sequence identities for the test sequences relative to the reference sequence, based on the program parameters.

A “comparison window,” as used herein, includes reference to a segment of any one of the number of contiguous positions selected from the group consisting of from 20 to 600, usually about 50 to about 200, more usually about 100 to about 150 in which a Sequence may be compared to a reference sequence of the same number of contiguous positions after the two sequences are optimally aligned. Methods of alignment of sequences for comparison are well-known in the an. Optimal alignment of sequences for comparison can be conducted, eg, by the local homology algorithm of Smith & Waterman, Adv. Appl. Math. 2:482 (1931), by the homology alignment algorithm of Needleman & Wunsch. J, Mol. Biol. 48:44} (1970), by the search for similarity method of Pearson & Lipman, Proc. Nat ‘I. Acad. Sci. USA 852444 (1988). by computerized implementations of these algorithms (GAP, BESTF 1'1‘, l-‘AS‘l‘/\, and TFASTA in the Wisconsin Genetics Software Package, Genetics Computer Group, 575 Science Dr., Madison, Wl), or by manual alignment and visual inspection (xee, eg, (lurrenl Protocols in Molecular Biology (Ausubel e1al., eds. l987-2005, Wiley lnterseienCe)).

A preferred example of algorithm that is suitable for detennining percent sequence identity and sequence similarity are the BLAST and BLAST 2.0 algorithms, which are described in Altschul et al., Nuc. Acids Res. 25:3389-3402 (1977) and Altschul at 01., J. M01. Biol. 2159103-410 (1990), respectively. BLAST and BLAST 2.0 are used, with the parameters described herein, to detennine percent sequence identity for the nucleic acids and proteins of the invention. Software for performing BLAST analyses is publicly available through the National Center for Biotechnology information. This algorithm involves first identifying high scoring sequence pairs (HSPs) by identifying short words of length W in the query sequence, which either match or satisfy some positive-valued threshold score T when aligned with a word of the same length in a database sequence. T is referred to as the neighborhood word score threshold (Altschul et a1. , supra). These initial neighborhood word hits act as seeds for lE09o467 initiating searches to find longer HSPs containing them. The word hits are extended in both directions along each sequence for as far as the cutnulative aligmnent score can be increased. Cumulative scores are calculated using, for nucleotide sequences, the parameters M (reward score for a pair of matching residues; always > 0) and N (penalty score for mismatching residues; always < 0). For amino acid sequences, a scoring matrix is used to calculate the cumulative score. Extension of the word hits in each direction are halted when: the cumulative alignment score falls off by the quantity X from its maximum achieved value; the cumulative score goes to zero or below, due to the accumulation of one or more negative~scoring residue alignments; or the end of either sequence is reached. The BLAST algorithm parameters W, T, and X determine the sensitivity and speed of the aligmnent. The BLASTN program (for nucleotide sequences) uses as defaults a wordlengtli (W) of 1 1, an expectation (E) of 10, M=5, N=- 4 and a comparison of both strands. For amino acid sequences, the BLASTP program uses as defaults a wordlength of 3, and expectation ([3) of 10, and the Bl .OSU M62 scoring matrix (see Henikoff & Henikoff, Proc. Natl. Acad. Sci. USA 89: 10915 (1089)) alignments (B) of 50, expectation (E) of 10, M=5, N=-4, and a comparison of both strands.

“Nucleic acid" refers to deoxyribonucleotides or ribonucleotides and polymers thereof in either single- or double—stranded fonn, and complements thereof.

The tenn encompasses nucleic acids containing known nucleotide analogs or modified backbone residues or linkages, which are synthetic, naturally occurring, and non- naturally occurring, which have similar binding properties as the reference nucleic acid, and which are metabolized in a manner similar to the reference nucleotides. Examples of such analogs include, without limitation, phosphorothioates, phosphoraniidates, methyl phosphonates, chiral-methyl phosphonates, 2-O-methyl ribonucleotides. peptide- nucleic acids (PNAS) By "nucleic acid hybrid" or "probeztarget duplex" is meant a structure that is a double-stranded, hydrogen-bonded structure, preferably about l0 to about 100 nucleotides in length, more preferably 14 to 50 nucleotides in length, although this will depend to an extent on the overall length of the oligonucleotide probe. The structure is sufficiently stable to be detected by means such as chemiluminescent or fluorescent light detection, autoradiography, electrochemical analysis or gel electrophoresis. Such hybrids include RNA:RNA, RNA:DNA_. or DNA:DNA duplex molecules. lE0904 "RNA and DNA equivalents" refer to RNA and DNA molecules having the same complementary base pair hybridization properties. RNA and DNA equivalents have different sugar groups (i.e., ribose versus deoxyribose), and may differ by the presence of uracil in RNA and thymine in DNA. The difference between RNA and DNA equivalents do not contribute to differences in substantially corresponding nucleic acid sequences because the equivalents have the same degree of complementarity to a particular sequence.

By "preferentially hybridize" is meant that under high stringency hybridization conditions oligonucleotide probes can hybridize their target nucleic acids to form stable probeztarget hybrids (thereby indicating the presence of the target nucleic acids) without fonning stable probeznon-target hybrids (that would indicate the presence of non—target nucleic acids from other organisms). Thus, the probe hybridizes to target nucleic acid to a sufficiently greater extent than to non-target nucleic acid to enable one skilled in the art to accurately detect the presence of (for example Candida) and distinguish these species from other organisms. Preferential hybridization can be measured using techniques known in the art and described herein.

By "theranostics" is meant the use of diagnostic testing to diagnose the disease, choose the correct treatment regime and monitor the patient response to therapy. The theranostics of the invention may be based on the use of an NAD assay of this invention on samples, swabs or specimens collected from the patient.

Object of the Invention It is an object of the current invention to provide sequences and/or diagnostic assays to detect and identify one or more yeast species. The current inventors have used the Ace.’ gene sequence to design primers and probes that are specific to Candida Ace2 genes. Such primers not only allow the detection of yeast and fungal species but also allow distinction between Candida species. The current invention further provides for primers and probes that allow discrimination between different Candida species.

Summafl of the Invention The present invention provides for a diagnostic kit for detection and identification of yeast species, comprising an oligonucleotide probe capable of binding to at least a portion of the Ace2 gene or its corresponding mRNA. The oligonucleotide IEOQO467 probe may have a sequence substantially homologous to or substantially complementary to a portion of the Ace2 gene or its corresponding mRNA. It will thus be capable of binding or hybridizing with a complementary DNA or RNA molecule. The Ace2 gene may be yeast Ace2 gene. The nucleic acid molecule may be synthetic. The kit may comprise more than one such probe. In particular, the kit may comprise a plurality of such probes. In addition the kit may comprise additional probes for other organisms, such as, for example, bacterial species or viruses.

The identified sequences are suitable not only for in vitro DNA/RNA amplification based detection systems but also for signal amplification based detection systems. Furthermore, the sequences of the invention identified as suitable targets provide the advantages of having significant intragenic sequence heterogeneity in some regions, which is advantageous and enables aspects of the invention to be directed towards group or species-specific targets, and also having significant sequence homogeneity in some regions, which enables aspects of the invention to be directed towards genus-specific yeast and fungal primers and probes for use in direct nucleic acid detection technologies, signal amplification nucleic acid detection technologies. and nucleic. acid in vitro amplification technologies for yeast and fungal diagnostics.

The Acc2 sequences allows for multi-test capability and automation in diagnostic assays.

One of the advantages of the sequences of the present invention is that the intragenic Ace2 nucleotide sequence diversity between closely related yeast species enables specific primers and probes for use in diagnostics assays for the detection of yeast to be designed. The Ace2 nucleotide sequences, both DNA and RNA can be used with direct detection, signal amplification detection and in vitro amplification technologies in diagnostics assays. The Ace2 sequences allow for multi-test capability and automation in diagnostic assays.

The kit may further comprise a primer for amplification of at least a portion of the Ace2 gene. Suitably the kit comprises a forward and a reverse primer for a portion otthc Aee2 gene.

The portion of the Ace2 gene may be equivalent to a portion of the region of the gene from base pair position 1736 to base pair position 2197 in C. albicans. Particularly preferred, are kits comprising a probe for a portion of the Ace2 Culbicans gene and / or a probe for a portion of the region of the gene equivalent to base pair position I736 to lE090467 p base pair position 2197 in C. albicans. Equivalent regions to base pair position 1736 to base pair position 2197 can be found in other organisms, but not necessarily in the same position.

The probe may preferentially hybridize to a portion of the Ace2 gene sequence selected from the group consisting of SEQ ID N03: 4-7 and 32-39 or their corresponding mRNA.

The kit may also comprise additional probes. The probe may have a sequence selected from the group consisting of SEQ ID Nos: 3, 30, 31, and a sequence substantially homologous to or substantially complementary to those sequences, which can also act as a probe for the Ace2 gene.

It is desirable that the probe has a sequence as defined by SEQ ID NO: 30.

The kit may comprise at least one forward in vilro amplification primer and at least one reverse in vitro amplification primer, the forward amplification primer having a sequence selected from the group consisting of SEQ ID Nos: 1, 20-24, and sequences bcin g substantially homologous or complementary thereto which can also act as a forward amplification primer, and the reverse amplification primer having a sequence selected from the group consisting of SEQ ID Nos: 2, 25-29, and a sequence being substantially homologous or complementary thereto which can also act as a reverse amplification primer. It is desirable that said forward primer sequence is selected from the group consisting of SEQ ID NOs:2l , 22, and 23, and said reverse primer sequence is selected from the group consisting of SEQ ID NOs:27, 28, and 29. The diagnostic kit may be based on direct nucleic acid detection technologies, signal amplification nucleic acid detection technologies, and nucleic acid in virro amplification technologies is selected from one or more of Polymerase Chain Reaction (PCR), Ligase Chain Reaction (LCR), Nucleic Acids Sequence Based Amplification (NASBA), Strand Displacement Amplification (SDA), Transcription Mediated Amplification (TMA), Branched DNA technology (bDNA) and Rolling Circle Amplification Technology (RCAT) ), or other in vilro enzymatic amplification technologies.

The invention also provides a nucleic acid molecule selected from the group consisting of SEQ ID NO.l to SEQ ID NO. 40 and sequences substantially homologous thereto, or substantially complementary to a portion thereof and having a function in diagnostics based on the Ace2 gene. lE0904 T he nucleic acid molecule may comprise an oligonucleotide having a sequence substantially homologous to or substantially complementary to a portion ofa nucleic acid molecule of SEQ ID NO.1 to SEQ ID NO. 40. The invention also provides a method of detecting a target organism in a test sample comprising the steps of: (i) Mixing the test sample with at least one oligonucleotide probe as defined above under appropriate conditions; and (ii) Hybridizing under high stringency conditions any nucleic acid that may be present in the test sample with the oligonucleotide to form a probertarget duplex; and (iii) Determining whether a probertarget duplex is present; the presence of the duplex positively identifying the presence of the target organism in the test sample.

The nucleic acid molecule and kits of the present invention may be used in a diagnostic assay to detect the presence of one or more yeast and/or fungal species, to inczisurc yeast and/or fungal titres in a patient or in a method of assessing the efficacy of a treatment regime designed to reduce yeast and/or fungal titre in a patient or to measure yeast and/or fungal contamination in an environment. The environment may be a hospital, or it may be a food sample, an environmental sample e.g. water, an industrial sample such as an in—process sample or an end product requiring bioburden or quality assessment.

The kits and the nucleic acid molecule of the invention may be used in the identification and/or characterization of one or more disruptive agents that can be used to disrupt the Ace2 gene function. The disruptive agent may be selected from the group consisting of antisense RNA, PNA, and siRNA. in some embodiments of the invention, a nucleic acid molecule comprising a species-specific probe can be used to discriminate between species of the same genus.

The oligonucleotides of the invention may be provided in a composition for detecting the nucleic acids of yeast and fungal target organisms. Such a composition may also comprise buffers, enzymes, detergents, salts and so on, as appropriate to the intended use of the compositions. It is also envisioned that the compositions, kits and methods of the invention, while described herein as comprising at least one synthetic oligonucleotide, may also comprise natural oligonucleotides with substantially the same sequences as the synthetic nucleotide fragments in place of, or alongside synthetic oligonucleotides.

E09046)’ The invention also provides for an in vitro amplification diagnostic kit for a target yeast and/or fungal organism comprising at least one forward in vitro amplification primer and at least one reverse in vitro amplification primer, the forward amplification primer being selected from the group consisting of one or more of or a sequence being substantially homologous or complementary thereto which can also act as a forward amplification primer, and the reverse amplification primer being selected from the group consisting of one or more of or a sequence being substantially homologous or complementary thereto which can also act as a reverse amplification primer.

The invention also provides for a diagnostic kit for detecting the presence of candidate yeast and/or fungal species, comprising one or more DNA probes comprising a sequence substantially complementary to, or substantially homologous to the sequence of the Aee2 gene of the candidate yeast andfor fungal species. The present invention also provides for one or more synthetic oligonucleotides having a nucleotide sequence substantially homologous to or substantially complementary to one or more ofthe group consisting ofthe Aee2 gene or mRNA transcript thereof, the yeast Aee2 gene or mRNA transcript thereof, the yeast Aee2 gene or mRNA transcript thereof, one or more of SEQ ID NO l-SEQ ID NO 40.

The nucleotide may comprise DNA. The nucleotide may comprise RNA. The nucleotide may comprise a mixture of DNA, RNA and PNA. The nucleotide may comprise synthetic nucleotides. The sequences of the invention (and the sequences relating to the methods, kits compositions and assays of the invention) may be selected to be substantially homologous to a portion of the coding region of the Aee2 gene. The gene may be a gene from a target yeast or fungal organism. The sequences of the invention are preferably sufficient so as to be able form a probeztarget duplex to the portion of the sequence.

The invention also provides for a diagnostic kit for a target yeast or fungal organism comprising an oligonucleotide probe substantially homologous to or substantially complementary to an oligonucleotide of the invention (which may be synthetic). It will be appreciated that sequences suitable for use as in vitro amplification primers may also be suitable for use as oligonucleotide probes: while it is preferable that amplification primers may have a complementary portion of between about 15 nucleotides and about 30 nucleotides (more preferably about 15-about 23, most lEo9o4 preferably about 20 to about 23), oligonucleotide probes of the invention may be any suitable length. The skilled person will appreciate that different hybridization and or annealing conditions will be required depending on the length, nature & structure (eg.

Hybridization probe pairs for LightCycler, Taqman 5’ exonuclease probes, hairpin loop structures etc. and sequence of the oligonucleotide probe selected.

Kits and assays of the invention may also be provided wherein the oligonucleotide probe is immobilized on a surface. Such a surface may be a head, a membrane, a column, dipstick, a nanoparticle, the interior surface of a reaction chamber such as the well of a diagnostic plate or inside of a reaction tube, capillary or vessel or the like.

The target yeast or fungal organism may be selected from the group consisting of C. albicans, C. lropicalis, C. glabrata, C. krusei, C. parapsilosis, C. tropicalis, C. dubliniensis, C. guiiliermondii, C. norvegien.ris, C. famata, C. haemuloni, C. kefvr, C. milix, (T viswanathii and Aspergillzzs species.

The target yeast organisms may be a Candida species for the given set of primers already experimentally demonstrated, and more preferably, selected from the group consisting of C. albicans C. tropicalis. Cdubliniensis, C. glabrata, C. /rru.s"ei, C. prmzpsilusis, C. guilliermondii, C. norvegiensis, C. famata, C. haemuloni, C. kejj/r, C. u/ilis, C’. viswanathii.

Under these circumstances, the amplification primers and oligonucleotide probes of the invention may be designed to a gene specific or genus specific region so as to be able to identify one or more, or most, or substantially all of the desired organisms of the target yeast organism grouping.

The test sample may comprise cells of the target yeast and/or fungal organism.

The method may also comprise a step for releasing nucleic acid from any cells of the target yeast or fungal organism that may be present in said test sample. Ideally, the test sample is a lysate of an obtained sample from a patient (such as a swab, or blood, urine, saliva, a bronchial lavage, dental specimen, skin specimen. scalp specimen, transplant organ biopsy, stool, mucus, or discharge sample). The test samples may be a food sample, a water sample an enviromnental sample, an end product, end product or in- process industrial sample.

The invention also provides for the use of any one of SEQ ID NO] to SEQ ID NO. 40 in a diagnostic assay for the presence of one or more yeast species. The species to an lEo9o4s7 16 may be selected from the group consisting of C. albicans C. tropicalis. C.dubliniensis, C. glabrata, C. krusei. C. parapsilosis, C. guilliermondii, C. norvegiensis, C. famata, C. liaemuloni, C. kefyr, C. utilis, C. viswanathii.

The invention also provides for kits for use in clinical diagnostics, theranostics, food safety diagnostics, industrial microbiology diagnostics, environmental monitoring, veterinary diagnostics, bio-terrorism diagnostics comprising one or more of the synthetic oligonuclec-tides of the invention. The kits may also comprise one or more articles selected from the group consisting of appropriate sample collecting instruments, reagent containers, buffers, labelling moieties, solutions, detergents and supplementary solutions. The invention also provides for use of the sequences, compositions, nucleotide fragments, assays, and kits of the invention in theranostics, Food safety diagnostics, Industrial microbiology diagnostics, Environmental monitoring, Veterinary diagnostics. Bio-terrorism diagnostics.

‘I "he nucleic acid molecules, composition. kits or methods may be used in a diagnostic nucleic acid based assay for the detection of yeast species.

The nucleic acid molecules, composition. kits or methods may be used in a diagnostic. assay to measure yeast or fungal titres in a patient. The titres may be measured in vitro.

The nucleic acid molecules, composition. kits or methods may be used in a method of assessing the efficacy of a treatment regime designed to reduce yeast and/or fungal titre in a patient comprising assessing the yeast and/or fungal titre in the patient (by in viva methods or in vim) methods) at one or more key stages of the treatment regime. Suitable key stages may include before treatment, during treatment and after treatment. The treatment regime may comprise an antifungal agent, such as a pharmaceutical drug.

The nucleic acid molecules. composition, kits or methods may be used in a diagnostic assay to measure potential yeast and/or fungal contamination, for example, in a hospital.

The nucleic acid molecules, composition, kits or methods may be used in the identification and/or characterization of one or more disruptive agents that can be used to disrupt the Ace2 gene fiinction. Suitable disruptive agents may be selected from the group consisting of antisense RNA, PNA, siRNA. lEo9o4e7 Brief description of the Figures Figure 1: Primers binding sites in (grey highlights) Ace2 gene in Candida albicans (XM_707274,l). The amplified region of interest is underlined (Position I736 to 2197).

Product size= 462 base pairs Figure 2: Location of C albicans probe P1-CanAce2 binding site (underlined and bolded in the amplified fragment of Ace2 gene. PCR primers CanAce2-F/CanAce2—R are highlighted.

Figure 3: Real-time PCR assay for C. albicans based on the Ace? gene with 'l‘aqMan probe Pl-CanAce2. Specificity of the assay was tested using a panel of DNA from four other Candida species and Aspergillusfumigatus. The three C. albicans strains tested were detected in the real-time PCR and there was no cross-reaction with DNA for other species.

Figure 4: Location of indicated C. albicans primers and probes. Figure 4(a) primer ACFI is marked in bold, while primer ACRI is marked in bold underline; Figure 4(b) primer AC1-‘Z is marked in bold and primer ACR2 is marked in bold underline; Figure 4(e) primer ACF3 is marked in bold and primer ACR3 is marked in bold underline; and Figure 41(1) probe is marked in bold, ACALBI on - strand, ACALB2 in + strand.

Primer (ACF2b/ACR3b) binding sites (grey highlights) and ACALBI probe (bold text) in Ace2 of Candida albicans (XM__707274.]). The amplified region of interest is underlined. (Position of the region of interest: 1879-2004,).

Figure 5: F igure 6: lnclusivity panel of C. albicans strains. Amplification plot from Real- timc PCR assay for C. albicans based on the Ace2 gene with TaqMan probe ACALBI and primer set ACF2b/ACR3b. Specificity of the assay was tested using a panel of DNA from 20 C. albicans strains and 84 strains covering 19 spp. of clinically relevant and related Candida. (a) The 20 C. albicans strains tested were detected. (b) No cross- reaction was seen with DNA from 34 strains covering 19 other Candida species. Signal obtained only from (+) controls.

Figure 7: Bxclusivity vaginitisf vaginosis panel. Amplification plot from Real- time PCR assay for C. albicans based on the Ace2 gene with TaqMan probe ACALBI and primer set ACF2b/ACR3b. A signal was obtained only for (+) control (C. albicans) samples. No signal was obtained for the organisms in the exclusivity panel.

Figure 8: Amplification plot from Real-time PCR assay for C. albicans based on the Ace2 gene with TaqMan probe ACALB1. Sensitivity of the assay was tested using lEo9o4e7 I8 various inputs of template DNA from C. albicans. The LOD of the assay was found to be ~l cell equivalent.

Detailed Description of the Drawiggs EXAMPLE 1 Materials and Methods Cell Culture Candida species were cultured in Sabouraud broth (4% wt/vol glucose, 1% wt/vol peptone, 1.5 % agar) for 48 hours at 37°C in a shaking incubator.

DNA Extraction Cells front Candida spp. were pre-treated with lyticase or zymolase enzymes prior to DNA isolation. DNA was isolated from Candida spp. using either the MagNA Pure System (Roche Molecular Systems) in combination with the MagNA pure Yeast and Bacterial isolation kit III according to the manufacturers protocol, or the Qiagcn DNeasy Plant Mini kit (silica-based DNA purification in spin column format).

DNA sequencing of Ace2 gene regions in Candida species The publicly available sequences of the Ace2 genes of Candida species were acquired from the NCBI database and aligned using ClustalW. The PCR Primer set, namely CanAce2~F/CanAce2-R (Figure 1, Table 1) was designed and used to amplify the Ace2 gene region in Candida spp. equivalent to base pair position 1736 to base pair position 2197 in C. albicans with primer set CanAce2-F/CanAce2-R. The Ace2 gene regions were amplified in C. albicans, C.tr0p1'calis and C. dubliniensis by conventional PCR on the iCycler BioRad PCR machine or the PTCZOO Peltier thermocycler (MJ Research) using the reagents outlined in Table 2 and the thennocycling conditions described in Table 3.

The PCR reaction products were purified with Roche High Pure PCR Product Purification kit or with the ExoSAP-IT kit (USB) according to the manufacturers’ protocol and subsequently sent for sequencing to Sequiserve, Germany using the forward amplification primer CanAce2-F. DNA sequence information was generated for three Candida species. (C. albicans, C. tropicalis and C. dubliniensis).

IEo9o4 Table 1: PCR primers designed to amplify the Acc2 gene regions in Candida spp.

Primer Name Primer Sequence Can/\cc2-F TATCACCTITGAAAAAACAATTACC CanAcc2-R CACCAACACAAATATTTCGATC Table 2: Conventional PCR reagents used to amplify the Acel gene regions in Candida spp.

PCR Reaction Mix SAMPLE x l x Buffer( 100 mM Tris HCl, 15 mM MgCl3, 500 mM KCI pH 5 pl 8.3) dN n3‘s Mix, Roche (lOmM dNTP) ‘ 1 pl Primer Forwzird CanAce2-F (10pM) 1 pl _Primer Reverse CanAce2-R (l0pM) I ul Polymerase TaqPol, Roche 1U/pl 1 pl ll3O Amgen/Accugene 36-39 gl Genomic DNA Template 2-5 pl TOTAL VOLUME 50 pl Table 3: Conventional PCR reaction conditions applied to amplify the Ace2 gene regions in Candida spp.

PCR Thermal profile Lid preheating was ON Step Temp Time I 94°C 1 min 2 S3 or 50°C 1 min 3 72°C 1 min 4 72°C 7 min 8°C Hold lEo9o4 Table 4: TaqMan probe for C. albicans based on Acel gene region P 1 —CanAce2 CTGTCACCATTGAATGGAGTCC AG Table 5: Real-time PCR reagents Preparation of PCR Reaction Mix SAMPLE LighIC_vcler®FastSIartDNA Master HybProbe, Roche Cat. O3 003 x 1 248 001 HybProb mix 10 x cone. (Red cap) '2 pl MgClg stock solution (Blue cap) (Final cone. in reaction is 3 mM) 1.6 pl Probe Pl -CanAce2 2 pl Primer Forward CanAce2-F I pl Primcr Reverse CanAc.e2-R I pl I-I30 l_’CI_{-grade 10.4 in] 'l'empl2itc 2 pl 'l'OTAI, VOLUME 20 in] Table 6: Real-time PCR thermocycling conditions PC R Thermal profile Cycle Step Temp Time Activation 1 95°C 10 min Amplification l 95°C 10 sec X 50 - 20 sec °C °C 10 sec Cooling I 40°C Hold lEo9o4e7 RES U/. TS Primer and Probe Design The sequence information available for the Ace2 gene in Candida spp. was aligned with the newly generated sequence information for the Ace2 gene in Candida spp. and analysed using bioinformatics tools. Species-specific probes were designed based on the compiled Ace2 sequence information for Candida albicans {Table 4).

Figures 2 shows the relative positions of the PCR primers and TaqMan DNA probe for the amplification and detection of C, albicans. The specificity of the TaqMan probes for the identification of C. albicans was demonstrated in a real-time PCR assay on the LightCycler using the reagents and thennocycling conditions outlined in Tables 5. For the C. albicans assay based on the Ace2 gene, PCR primers CanAce2-F/Ca.nAce2—R were combined with TaqMan probe, Pl-CanAee2. The specificity of the assay for the detection of C. albicans was confirmed by including DNA from a range of closely related Candida species and A. fwnigalus species in the C. a/l7ic'ur1s real-time PC R assay. The assay detected C. albicam‘ but did not detect or cross-react with DNA from any other Candida species tested or with A. fumigalus DNA. Figure 3 shows the C. albicans real~time PCR assay and the specificity of the assay for C. albicans.

EXAMPLE 2 Primers and probes for specific detection and identification were designed following in silico analysis of generated sequences. Three forward and three reverse primers were generated and two probes were designed as follows. Figures 4(a) to 4(d} discloses the location of these sequences in the Ace2 subsequence.

ACFI: SEQ ID NO:20: ATCAAAGAATCATCACCA ACF2: SEQ ID NO:2I: AGACTTCATTGTTACCAC ACF3: SEQ ID NO:24: CACCAGGTGAATTGG ACR] : SEQ ID N0:25: CATTGTATCGACGAGTG ACR2: SEQ ID NO:26: TGTATCGACGAGTGAAT ACR3: SEQ ID NO:27: TTCGCACATTGTATCG lE09o4ACALB1: SEQ ID NO:30: 6FAM-ATATCTTATCCTCATCCGGTCCT--BHQI ACALB2: SEQ ID NO:3l: 6F AM-AGGACCGGATGAGGATAAGATAT--BHQI The primer sets were evaluated using the following assay conditions: UNG treatment: 50°C 2min followed by 95°C lmin. The amplification included 50 cycles, 95°C l0sec, 60°C 30 sec, followed by a 2 min cooling at 40°C.

Based on initial assay performance (eg. fluorescence and efficiency), primer set ACF 3/ ACR3 was chosen for further evaluation using ACALBI probe. Initial inclusivity and exclusivity experiments were performed to evaluate the potential of the assay using the chosen assay oligonucleotides. Specificity of the assay was tested using a panel of DNA from 14 C. albicans strains and 23 strains representing 19 other Candida species. All 14 C. albicans strains tested were detected. No cross-reaction was seen with DNA from [9 the other Candida species, i.e., signal was obtained only from the positive C. albicans control.

The Ace2 assay was shown to be specific to C. albicans, and initial performance was good under conditions tested.

Next, eight different combinations of primers were tested in order to red ucc cycling times. The following conditions were tested: UNG treatment for 2min at 50°C, lmin at 95°C, followed by amplification of 50 cycles, 95°C Ssec, 60°C 10sec. followed by :1 cooling step of 2min at 40°C.

The combination of primer set ACF2/ACR3 and the ACALB] probe performed the best under these conditions. The LOD of the assay is ~11-10 cell equivalents. This primer combination demonstrated higher fluorescence at lower template inputs, and 3 out of 3 one-cell equivalents were detected with earlier C p values. Slight modifications were made to the primer sequences in order to further shorten cycle times, while retaining sensitivity and specificity (Table.7}. lEo9o457 Table 7 : Modifications to primer sequences Primer name SEQ ID NO Tm ACF2 2| 53°C ACF2b 22 57. 1°C ACFZC 23 595°C ACR3 27 527°C ACR3b 28 568°C ACR3c 29 602°C Further reduced cycling conditions were tested, i. e., amplification step ot‘95°C for I second and 60°C for 10 seconds. l0-fold dilutions of C. albicans DNA were prepared and inputs of 1x105 to 0.1 cell equivalents were used as template. The combination of ACF2b and ACR3b primers were selected for inclusivity and exclusivity testing due to higher fluorescence at lower template inputs and 3 out of} one-cell equivalents were detected with earlier Cp values than other primer sets, as indicated in Table 8.

Table 8: CI’ values obtained for different Tm primer sets.

Efor iAcR3b A .c.PV_. .19 - 39 Twenty strains of Candida albicans were selected to demonstrate inclusivity of detection with this primer set (see Table 9, Figure 5 and Figure 6). Real-time PCR assay for C. albicans was carried out as described with TaqMan probe ACALBI and primer set ACF2b/ACR3b. All twenty C. albicans strains tested were detected, and no signal obtained from (-) controls (see Figure 6(a)). lE090457 24 "£2; C. albicans strains used in inclusivity experiments Calbtccns B 3345 C.albi¢.-ans 3328 C.a.lbecans 173 C.alb;'c.:r-s isolate "isolate 320 isolate I6 755 Isolate S8? with 1560 lumen: ulosls 9569 than: Cmdraemia AIDS untecled skin at Child asthma ol met from dead from 19» mouth of Chlld \\\\\'\\'\\\\'\\\\\'\'\'\‘\ In order to demonstrate exclusivity of the assay, the Acel assay was tested for perfonnanee against 84 strains covering 19 spp. of clinically relevant and related ('am1z‘da (see Table 10 below). In order to ensure that all DNA tested is PC R ampliliable, the Candida DNA samples were amplified with universal fungal primers U1 and U2. All DNA tested was shown to be PCR amplifiable. A template input of E05 CE/rxn was used, which is higher than normally tested. A higher input was tested because the organisms tested are related Candida and Ace2 sequence information was not confirmed for 17 species prior to testing. Each input was tested in triplicate. No cross-reactions were observed, demonstrating the specificity of the Aee2 assay for C . albicans detection (see Figure 6(b)). lEo9o467 3 Egg Candida Specificity panel - Clinically relevant and related Candida spp.

C. amlcans Ace2 - Tested in ate . PHLS NCPF ' 95 . PHLS NCPF PHLS NCPF .76 ATCC . IHEM , Leuven 9555 IHEM gels ' C33 883 C88 851 CBS C CBS — New Zealand. Masts-non PLHS NCPF UK PLHS NCPF UK IHEM Brussels IHEM Grenoble, France CBS 9 CBS ‘ inl ' E , Cain: CBS hand H CBS , ol53- e USA CBS man. blood at aul USA, New York CBS blood 19 France_ Paris IHEM rance IHEM Lanka CBS from case Mnlana CBS from infecled ' Buonos AJIBS CBS um Lanka PHLS NIZPF ' PHLS NCPF blood Pl'l_S NCPF fislula DSMZ or 3 DSMZ faeces n/3 ATCC wound exas IHEM Human nanl Gosselies CBS Puerlo Rico CBS na CB8 Domnnacan CBS bladder Denmask‘ C IHEM human eat canal ' CBS ATCC unknown ATCC Blood iEo9o4e7 26 C.a’ub1z'm'ensis IHEM ame stmn as 3949 C.dubIim’en.sis IHEM mou1h on Fnance C.dubl1'nim.9Js IHEM um Brussels.

C.a'ubIiniensis CBS oral cavit ,Vicloria. Melbourne C.a'ubI1mm.s'1.s' CBS of HIV Ireland Dublin C.a’ub!mien.szs 088 of 38- Netherlands Cdubfinierxszs CBS with neut Netherlands, C.h5si£arue P|*LS NCPF . UK C.lu&1ame IHEM fruit lsreal C.1ua‘£am'e CBS from New Zealand C.lusiLame IHEM USA C.Iu&1'.ram'e IHEM blood It , Mulano PHLS NCPF wilh UK CBS of ' man CBS CBS semen of bull UK CBS lesion 1! nail fuel st USA sake starler east of Man ? Norwa human urine , Bmssels . of herlands. Gouda mmtrale Dordrecht with infected l ds citem)’ C. catemdata C. catwulata eratnmc foot C. sake es hansenii C. DSMZ cheese hansenn CBS on toe DSMZ estinal tract of PHLS NCPF , ‘ UK DSMZ aka ces marxnanus DSMZ dal as E DSMZ of Trifolium n/3 C. utifis DSMZ east from German‘ C. uiiiis DSMZ from nla C.vz'swarxathz':‘ CBS cerebro- ’ fluid C.vi.swa2:a1hii CBS C. CBS C’. DSMZ lEo9o4 Exclusivity was further demonstrated using a vaginitis/vaginosis panel with 45 species of clinically relevant organisms in triplicate (see Table 11 below) using the shorter cycle conditions. A template input of ~10‘ CE/rxn was used. No cross- reactions were observed, further demonstrating the specificity of the Ace2 assay (see Figure 7).

‘I 2 3 C 6 7 8 9 U 1 an tobatfcr lalo ffii ftnca/x'_r the rr'c+ua to/I’ Azrin Vitus I laxvtrus 2 Anna wry: //mvcr yum’ kbx/2 lb crrobizrt/tar on-/ob or/llur or/.1- ' actob ac/M4: /:5: A-ia Pm P/vleur mu-um://I 17/no few" P/-onakncm Jign/-I/‘I 9:3:/dc-mona- Pxa m1om¢v@' an vi:/:3 rraha amau: ra/Ivar/us Table 11: Vaginosis/Vaginitis specificity panel organisms tested against Ace2 assay. l3644 30030 7457 15529‘ V11-34 BB 8090 u9a9 13047 zu37i 20477’ annsa 4944 R.92I—O00 IA D6000 A 1A 1A - 07.000 03754400 00755400 30I04‘ 20079‘ 20055 4364 5707' M994 6998 ' 2oa1s' 20707’ ‘ 2140 4539 aoovr 29r 70449 I600 34¢ 20044 20373‘ ' 30001 Probit analysis was performed in order to statistically determine. the LOD (limit of detection) of the Ace2 assay using ACF2b/ ACR3b/ ACALB] with shorter cycle times. The LOD of the Ace? assay was determined by testing 8 template inputs and [2 replicates. C. aibicans strain CBS 562 was selected for LOD determination.

The results are shown below in Table 12 and Figure 8. An LOD of 0.839, with a probability of greater than or equal to 95% was found by Probit analysis. lEo9o4s7 flleflg Input levels (cell equivalents) and results of Probit analysis Number of replicates Input level Number of replicates tested detected I0 12 12 5 12 g 12 4 l2 l2 3 12 12 2 12 ll 1 12 1 1 0.5 12 L_ l 0.} l2 Discussion The number of yeast and fungal infections among immuno-compromised patients is escalating. Contributing to this increase is the growing resistance of many yeast and fungal species to antifungal drugs. There is, therefore, a need to develop a last. accurate diagnostic method to enable early diagnosis of yeast and fungal species.

Early diagnosis will enable the selection of a specific narrow spectrum antibiotic or antifungal to treat the infection‘ The current invention provides for sequences and/or diagnostic assays to detect and identify one or more yeast and fungal species. The current inventors have exploited the sequence of the Ace2 gene in Candida species to design primers and probes specific for regions of this gene. Ace2 is an ideal candidate for the design of primers and probes directed towards the detection of yeast and fungal species-specific targets and for the detection of genus specific diagnostic targets respectively. The current invention allows the detection of yeast and fungal species but also allows distinction between Candida species.

Summary Using newly generated and publicly available sequences, the inventors have designed new primers and probes that are surprisingly specific to Candida Acel polynucleotide sequences under short cycle times identified here. Such primers and probes not only allow the detection of yeast and fungal species but also allow surprisingly effective distinction between Candida species and specific detection of C. albfcans, even under short cycle times. The current invention further provides for IEOQO4 primers and probes that allow excellent discrimination between different Candida species.

The words “comprises/comprising” and the words “having/including" when used herein with reference to the present invention are used to specify the presence of stated features, integers, steps or components but does not preclude the presence or addition of one or more other features, integers, steps, components or groups thereof.

It is appreciated that certain features of the invention, which are, for clarity, described in the context of separate embodiments, may also be provided in combination in a single embodiment. Conversely, various features of the invention, which are. for brevity. described in the context of a single embodiment, may also be provided separately or in any suitable sub-combination.

In so far as any sequence disclosed herein differs from its counterpart in the attached sequence listing in PatentIn3.3 software, the sequences within this body oftcxt are to be considered as the correct version.

Claims (1)

1. Claims . A diagnostic kit for a yeast or fungal species comprising an oligonucleotide probe capable of binding to at least a portion of the Ace2 gene or its corresponding mRNA. A kit as claimed in claim I, wherein the portion of the Ace2 gene is a portion of the region of the gene from base pair position 1736 to base pair position 2197 C. albicans Ace2 gene. A kit as claimed in any of claim 1 or claim 2, wherein the probe is selected from the group consisting of SEQ 1]) N05: 3, 30, 31 or sequences substantially similar or complementary thereto which can also act as a probe, and/or wherein the kit further comprises a forward amplification primer being selected from the group consisting of SEQ ID Nos: 1, 20-24, and sequences substantially similar or complementary thereto which can also act as a forward amplification primer and a reverse amplification primer being selected from the group consisting of SEQ ID N05: 2, 25-29, and sequences substantially similar or complementary thereto which can also act as a reverse amplification primer.. A nucleic acid molecule selected from the group consisting of: SEQ ID NO 1 through SEQ ID N O 40 and sequences substantially homologous or substantially complementary thereto or to a portion thereof and having a function in diagnostics based on the Ace2 gene. A kit substantially as described herein with reference to the accompanying figures.