Ehsanollah Ghaznavi-Rad

Dr. Ehsanollah Ghaznavi-Rad

Arak University of Medical Sciences

Research Focus & Metrics

Academic Career Length

18Years (2009-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 January 2012 in Journal of Biomedicine and Biotechnology
Verified
Journal Article
Open access
PDF file
Salman AtshanSalman Atshan
Salman Atshan
MSMariana Nor Shamsudin
Mariana Nor Shamsudin
ZSZamberi Bin Sekawi
Zamberi Bin Sekawi
LTLeslie Thian Lung Than
Leslie Thian Lung Than
RHRukman Awang Hamat
Rukman Awang Hamat
PCPei Pei Chong
Pei Pei Chong
Clinical information about genotypically different clones of biofilm-producingStaphylococcus aureusis largely unknown. We examined whether different clones of methicillin-sensitive and methicillin-resistantS. aureus(MSSA and MRSA) differ with respect to staphylococcal microbial surface components recognizing adhesive matrix molecules (MSCRAMMs) in biofilm formation. The study used 60 different types ofspaand determined the phenotypes, the prevalence of the 13 MSCRAMM, and biofilm genes for each clone. The current investigation was carried out using a modified Congo red agar (MCRA), a microtiter plate assay (MPA), polymerase chain reaction (PCR), and reverse transcriptase polymerase chain reaction (RT-PCR). Clones belonging to the samespatype were found to have similar properties in adheringto thepolystyrene microtiter plate surface. However, their ability to produce slime on MCRA medium was different. PCR experiments showed that 60 clones of MSSA and MRSA were positive for 5 genes (out of 9 MSCRAMM genes).icaADBCgenes were found to be present in all the 60 clones tested indicating a high prevalence, and these genes were equally distributed among the clones associated with MSSA and those with MRSA. The prevalence of other MSCRAMM genes among MSSA and MRSA clones was found to be variable. MRSA and MSSA gene expression (MSCRAMM andicaADBC) was confirmed by RT-PCR.

1 March 2010 in Journal of Clinical Microbiology
Verified
Journal Article
Closed access
EGEhsanollah Ghaznavi-Rad
Ehsanollah Ghaznavi-Rad
MSMariana Nor Shamsudin
Mariana Nor Shamsudin
ZSZamberi Bin Sekawi
Zamberi Bin Sekawi
LKLiew Yun Khoon
Liew Yun Khoon
MAMohammad Nazri Aziz
Mohammad Nazri Aziz
VNVasantha Kumari Neela
Vasantha Kumari Neela
We define the epidemiology of predominant and sporadic methicillin-resistant Staphylococcus aureus (MRSA) strains in a central teaching and referral hospital in Kuala Lumpur, Malaysia. This is done on the basis of spa sequencing, multilocus sequence typing (MLST), staphylococcal cassette chromosome mec (SCC mec ) typing, and virulence gene profiling. During the period of study, the MRSA prevalence was 44.1%, and 389 MRSA strains were included. The prevalence of MRSA was found to be significantly higher in the patients of Indian ethnicity ( P < 0.001). The majority (92.5%) of the isolates belonged to ST-239, spa type t037, and possessed the type III or IIIA SCC mec . The arginine catabolic mobile element (ACME) arcA gene was detected in three (1.05%) ST-239 isolates. We report the first identification of ACME arcA gene-positive ST-239. Apart from this predominant clone, six (1.5%) isolates of ST-22, with two related spa types (t032 and t4184) and a singleton (t3213), carrying type IVh SCC mec , were detected for the first time in Asia. A limited number of community-acquired (CA) MRSA strains were also detected. These included ST-188/t189 (2.1%), ST-1/t127 (2.3%), and ST-7/t091 (1%). Panton-Valentin leukocidin (PVL) was detected in all ST-1 and ST-188 strains and in 0.7% of the ST-239 isolates. The majority of the isolates carried agr I, except that ST-1 strains were agr III positive. Virulence genes seg and sei were seen only among ST-22 isolates. In conclusion, current results revealed the predominance of ST-239-SCC mec III/IIIA and the penetration of ST-22 with different virulence gene profiles. The emergence in Malaysia of novel clones of known epidemic and pathogenic potential should be taken seriously.

1 December 2009 in Journal of Clinical Microbiology
Verified
Journal Article
Open access
VNVasantha Kumari Neela
Vasantha Kumari Neela
AZArif Mohd Zafrul
Arif Mohd Zafrul
NMNor Shamsudin Mariana
Nor Shamsudin Mariana
ABAlex van Belkum
Alex van Belkum
YLYun Khoon Liew
Yun Khoon Liew
EGEhsanollah Ghaznavi-Rad
Ehsanollah Ghaznavi-Rad
Methicillin-resistant Staphylococcus aureus (MRSA) of sequence type 398 (ST398) has frequently been detected in pigs and pig handlers. However, in Malaysia, sampling 360 pigs and 90 pig handlers from 30 farms identified novel ST9- spa type t4358-staphylococcal cassette chromosome mec type V MRSA strains that were found to transiently colonize more than 1% of pigs and 5.5% of pig handlers.

1 October 2010 in Journal of Medical Microbiology
Verified
Journal Article
Closed access
EGEhsanollah Ghaznavi-Rad
Ehsanollah Ghaznavi-Rad
MSMariana Nor Shamsudin
Mariana Nor Shamsudin
ZSZamberi Bin Sekawi
Zamberi Bin Sekawi
ABAlex van Belkum
Alex van Belkum
VNVasanthakumari Neela
Vasanthakumari Neela
A multiplex PCR assay was developed for the identification of major types and subtypes of staphylococcal cassette chromosome mec (SCCmec) in meticillin-resistant Staphylococcus aureus (MRSA) strains. The method uses a novel 9 valent multiplex PCR plus two primer pairs for S. aureus identification and detection of meticillin resistance. All 389 clinical MRSA isolates from Malaysia and 18 European isolates from the Harmony collection harbouring different SCCmec types that we tested were correctly characterized by our PCR assay. SCCmec type III and V were by far the most common types among both hospital- and community-acquired Malaysian MRSA isolates, with an apparent emergence of MRSA harbouring the IVh type.

1 November 2013 in International Journal of Infectious Diseases
Verified
Journal Article
Closed access
AJAlireza Japoni-Nejad
Alireza Japoni-Nejad
MRMohsen Rezazadeh
Mohsen Rezazadeh
HKHamid Kazemian
Hamid Kazemian
NFNasimeh Fardmousavi
Nasimeh Fardmousavi
ABAlex van Belkum
Alex van Belkum
EGEhsanollah Ghaznavi-Rad
Ehsanollah Ghaznavi-Rad

1 February 2012 in Gene
Verified
Journal Article
Closed access
Salman AtshanSalman Atshan
Salman Atshan
MSMariana Nor Shamsudin
Mariana Nor Shamsudin
LTLeslie Thian Lung Than
Leslie Thian Lung Than
KLKing-Hwa Ling
King-Hwa Ling
ZSZamberi Bin Sekawi
Zamberi Bin Sekawi
EGEhsanollah Ghaznavi-Rad
Ehsanollah Ghaznavi-Rad