The technique used to investigate the genes responsibility for the virulence factor in P. mirablis is Single Polymerase Chain Reaction Technique. This has been conducted through using segments of the DNA with restricted number of nucleotides (oligonucleotide). Their action is to be primers specialized for virulence genes in P. mirablis., hpmB is also included and it is responsible for producing hemolycin P. mirabilis b-hemolysin that is different from other Proteus spp. It is organized by two genes, (hpmA and hpmB) that encodes the hpmA and hpmB proteins respectively^7,8.

The present study shows that hpmB gene is present in all 7 isolates at rate (100%) from urine samples of RA patients as shown in fig (1). The results contest the result which is verified by Al-Jumaily and Zgaer.  In their study, it is declared that the frequency of this gene in P. mirablis isolates is %100; that is isolated from patients suffering from urinary tract infections⁹. While Cestari et al., 2013 find the ratio of this gene in bacterial isolates comprising 96.24 % existing amplification for the hpmA and hpmB genes by PCR.⁶. The a-hemolycin toxin acts as a destroyer to the leukocyte membrane through creating small holes in the leukocyte membrane and epithelial cell. So, its presence is a vital factor in supplying the bacteria with iron and because of having the cytotoxic effects, this could lead to the destruction of the host kidney tissue¹⁰. Isolates with hpmA gene in them is in compatibility with the characterization presented by Uphoff and Welch (1990) who state the necessity of cleaving the N-terminal peptide of the hpmA by hpmB for the purpose of activating and transporting the hemolytic hpmA protein out of the cell⁸. This standard indicates that hpmA is a factor in the pathogenesis of P. mirabilis samples isolated from human urine¹⁰. Among the other results are those reported by Swihart and Welch,1990 refering that all P. mirabilis strains as having hpmA but HlyA is not detected in P. mirabilis isolates and is found only in 2 of the 24 P. vulgaris strains examined. Since P. mirabilis composes most (97%) of the Proteus urinary tract isolates, this suggests that hpmA is the predominant Proteus hemolysin and might play a role in extra intestinal infections caused by Proteus spp¹¹. These positive isolates with hpmB gene are also checked to confirm their ability to produce hemolysin on blood agar and it has been found that all the isolates (100%) have the ability to produce hemolysin. These results agree with the results of Sosa et al. (2006) and AL-Jumaa et al. (2011), who demonstrate that all isolates (100%) of Proteus bacterium which are isolated from different clinical sources exhibit hemolysis on blood agar plates, but Mishara et al. (2001) find that (85.14%) of Proteus isolates produce a-hemolysis while other isolates produce b –hemolysis on blood agar plate^12,13,14. The results of the study demonstrate that the detection of hpmB gene by PCR is sensitive enough to be used for discovering these virulence factors produced by P. mirabilis. The PCR technique is shown to be precise, fast, cheap and more accurate therefore this suggests that hpmB could be used as a diagnostic tool for P. mirablis bacterium.

Fig. 1. Agarose gel electrophoresis (2% agarose, 75 V for 1:45 hour) of hpmB and PCR products (422bp) codify for a-hemolysin of P. mirabilis isolates. Lane 1DNA ladder), 100-1100bp molecular marker, lanes 2 ,3,4,5,6,7,8,9,10 isolates were positive results

DNA sequencing analysis
Analyzing DNA sequence of hpmB gene
Three isolates were sequenced by Macrogen/Korea. The nucleotide switch is firmed by comber. The data are obtained from gene bank available at NCBI (https://www.ncbi.nlm.nih.gov). The results of gene sequence analysis hpmB show that there are two polymorphism in 2 isolates of the gene hpmB as shown in fig (2) and table (1). In the isolation of P. mirabilis (MF993448) Thymine nucleotide substitutions to Adenine is found at locus 2389107 and Cytosine has substitutions to Thymine at locus 2389062 . Finally, the results show  nonsense polymorphism as predict . Also, the results show silent variation and this type of variation doesn’t change the sequence of amino acid in the protein and doesn’t alter protein function as shown in table (1)¹⁵. Samples (MF993446) show 100 % identity for hpmB in comparison to the same genes of the CP017085.1. While samples, (MF993448) show 99 % identity for hpmB in comparison to the same genes of the : CP020052.1 strain.

Table (1):
Primer sequence of hpmB  geneand PCR condition

Table (2):
Identity of hpmB gene sequence in

Table (3):
polymorphism of hpmB gene sequence

Table (4):
Alignment of hpmB gene sequence Proteus mirabilis strain T18

Table (5):
Alignment of hpmB gene sequence Proteus mirabilis strain AR_0059

Table (6):
Alignment of hemolysin activation protein [Proteus mirabilis]

Table (7):
Alignment of hemolysin activation protein [Proteus mirabilis]

Fig. 2. Phylogenetic tree of Proteus species based on hpmB gene sequence analysis.

It is noticed, through the process of sequencing of the a-hemolysin at P. mirabilis, that it consists of two genes hpmA and hpmB⁷. P. mirabilis hemolysin hpmA investigation and description is necessary to clarify its significance as a virulence factor. Furthermore, it might have a possible association with other elements that are produced by P. mirabilis. These altogether could contribute to cytotoxicity in the UTIs of humans⁷. Mordi and Momoh.(2009)  find that a change in the amino acid or replacement with other amino acid may lead to a change in the nature of protein or output and thus lead to the emergence of strains resistant or sensitive to antibiotics[16]. The hpmA and hpmB genes are sequenced from local isolated samples presented 98 % identity for hpmA and hpmB compared to the same genes of the HI4320 (wild strain) (NCBI GenBank Number NC_010554.1). When the samples of the study are compared with each other 100 % identity is found among these genes¹⁷. The results of the study display that the amino acid remained the same and  that indicates variation from the silent type. In contrast, there is a study conducted on hpmB gene like Strauss et al., (1997) find that mutations enhance the function of hpmB (increase in hemolytic activity). This increasing in hemolytic activity could be a result of hpmB activating and secreting more hpmA¹⁸. Genotyping works to establish the relationship between bacteria strain on the basis of their genetic content uses. Many genotyping methods become important in the field of genealogy, classification of bacteria, identification of sources, method of infection and the differentiation of strain of high virulent bacteria to prevent their spread and elimination¹⁹. Therefore, the study finds a great importance in the genetic sequence of P. mirabilis virulence factors. The study finds that variant isolates possess polymorphism in hpmB genes.

A phylogenic tree based on the hpmB  gene
Molecular phylogenetic is a branch of phylogeny that analyzes hereditary molecular differences mainly in DNA sequences to gain information on an organisms’ evolutionary relationships²⁰. The identified genetic profile of any bacteria by a specific genotyping method can be as unique as fingerprint²⁰.

However, phylogeny estimated from a single gene should be treated with caution^21,22. The phylogenetic tree derived from hpmB gene sequences of clinical strains of 2 samples Proteus mirabilis with other sequences is available at NCBI showed in (Fig.2). As to be seen in the this figure, P. mirabilis (MF993443 ) lies in the same branch of the phylogenetic tree with P.mirabilis (WP_088207120.1).

Sequences of 16SrRNA with the size of 1.5 Kb is considered and widely used in bacterial taxonomy because it contains high conservation region which has variable region in different species. Furthermore, the most important was that 16SrRNA gene which could be sequenced easily²². On the other hand, the sensitivity of this approach is questioned particularly among human bacterial closely related to Enterobacteriaceae, which includes many common pathogens because of the high degree of conservation in species²². Therefore, the use of other genes rather than16SrRNA gene and the distinction between bacteria at the species level is regarded as a very important issue²³. Results indicate that since there is an increase in clinical significance of P. mirabilis, the choice of effectual molecular methods is of great epidemiological reputation. Bacterial genotyping opened new chances on epidemiological studies by the documentation of clinical and ecological isolates, the assessment of this association, the watching of clone propagation and the classification of bacterial populations within more or less constrained environments²⁴. By joining molecular phylogeny with traditional approach such as morphological, physiological and biochemical characteristics, bacteria identification could be achieved in a more accurate way^25,26.