key: cord-017948-fqhl1qb4
authors: Hu, Yuan
title: Molecular Techniques for Blood and Blood Product Screening
date: 2012-04-05
journal: Advanced Techniques in Diagnostic Microbiology
DOI: 10.1007/978-1-4614-3970-7_28
sha: 
doc_id: 17948
cord_uid: fqhl1qb4

The Food and Drug Administration (FDA) is responsible for ensuring the safety of the more than 15 million units of blood and blood components donated each year in the United States. “Blood banking has become a manufacturing industry, an industry that must conform to high standards and quality control requirements comparable to those of pharmaceutical companies or other regulated industries,” said David A. Kessler, MD, former FDA commissioner [1]. Screening donated blood for infectious diseases that can be transmitted through blood transfusion is a very important step in ensuring safety. The United States has the safest blood supply in the world [1] and the FDA is striving to keep it safe by decreasing the risk of infectious disease transmission. The regulatory agency is continuously updating its requirements and standards for collecting and processing blood. As mentioned earlier, an important step in ensuring safety is the screening of donated blood for infectious diseases. In the United States, tests for infectious diseases are routinely conducted on each unit of donated blood, and these tests are designed to comply with regulatory requirements (Table 28.1). The field of clinical microbiology and virology are now focusing on molecular technology. Currently, nucleic acid testing techniques have been developed to screen blood and plasma products for evidence of very recent viral infections that could be missed by conventional serologic tests. It is time for all blood safety procedures to include molecular detection techniques. This approach can significantly aid in blood safety to reduce the risk of transmission of serious disease by transfusion. This chapter reviews the current antigen/antibody-based technology, molecular biological technology, and published regulatory policy data for blood safety.

The Food and Drug Administration (FDA) is responsible for ensuring the safety of the more than 15 million units of blood and blood components donated each year in the United States. "Blood banking has become a manufacturing industry, an industry that must conform to high standards and quality control requirements comparable to those of pharmaceutical companies or other regulated industries," said David A. Kessler, MD, former FDA commissioner [ 1 ] . Screening donated blood for infectious diseases that can be transmitted through blood transfusion is a very important step in ensuring safety. The United States has the safest blood supply in the world [ 1 ] and the FDA is striving to keep it safe by decreasing the risk of infectious disease transmission. The regulatory agency is continuously updating its requirements and standards for collecting and processing blood. As mentioned earlier, an important step in ensuring safety is the screening of donated blood for infectious diseases. In the United States, tests for infectious diseases are routinely conducted on each unit of donated blood, and these tests are designed to comply with regulatory requirements (Table 28 .1 ). The fi eld of clinical microbiology and virology are now focusing on molecular technology. Currently, nucleic acid testing techniques have been developed to screen blood and plasma products for evidence of very recent viral infections that could be missed by conventional serologic tests. It is time for all blood safety procedures to include molecular detection techniques.

Y. Hu (*) U.S. Food and Drug Administration, Northeast Regional Laboratory , 158-15 Liberty avenue , Jamaica , NY 11433 , USA e-mail: yuan.hu@fda.hhs.gov No of fi cial support or endorsement of this article by the Food and Drug Administration is intended or should be inferred. This approach can signi fi cantly aid in blood safety to reduce the risk of transmission of serious disease by transfusion. This chapter reviews the current antigen/antibody-based technology, molecular biological technology, and published regulatory policy data for blood safety.

Direct detection of viral antigens and virus speci fi c antibodies has been a common tool for the diagnosis of virus infections in the past 40 years. There are some limitations. For direct detection of virus antigens, shortly after virus infection, only a few viruses release antigens in amounts suf fi ciently detectable in the body by an antibodymediated assay. For indirect virus detection by virus speci fi c antibodies (e.g., an immuno fl uorescence assay or enzyme immunoassay (EIA), etc.), there is a problem in that shortly after infection by a pathogenic virus, there is a window period in which antibody generation is insuf fi cient for detection [ 2 ] . To reduce this window period of low detection, direct nucleic acid tests are needed.

Through the application of molecular biology, biological and biochemical analyses have been revolutionized, and nucleic acid, gene-based techniques have been developed to screen blood and plasma donations for evidence of very recent and earlier viral infections that might otherwise be missed by conventional serologic testing. The nucleic acid tests can also provide evidence for genetic variation in viruses. Molecular methods include the use of nucleic acid probes as well as ampli fi cation-based and DNA sequence-based techniques. An increasing number of molecular diagnostic methods are now available commercially. In comparison to classical methods, molecular biological methods are superior in terms of rapidness, speci fi city, and sensitivity. The current nucleic acid detection methods in the fi eld may be grouped into two major classes: amplifying techniques such as PCR and nonamplifying techniques such as Southern blot hybridization. Amplifying techniques are more sensitive than nonamplifying techniques. There are two different types of amplifying methods [ 3 ] , target ampli fi cation methods and signal ampli fi cation methods. Target amplifying techniques include PCR, nucleic acid sequence-based ampli fi cation (NASBA) [ 4, 5 ] , self-sustaining sequence ampli fi cation (3SR), transcription-based ampli fi cation (TAS), transcription-mediated ampli fi cation (TMA), strand displacement ampli fi cation (SDA), and ligase chain reaction (LCR). Signal ampli fi cation methods include branched DNA (bDNA) signal ampli fi cation [ 6 ] , cleavage-based signal ampli fi cation (cycling probe technologies and invader assay), Qß replicase, hybrid capture, cycling probe technologies (CPT), and rolling-circle ampli fi cation (RCA) [ 7 ] . To further insure the safety of blood products, it is of importance to further improve these and other types of nucleic acid testing.

Southern blotting [ 8 ] was named after Edward M. Southern who developed this procedure at Edinburgh University in the 1970s. This technique is used to detect speci fi c sequences within mixtures of DNA, which is size-fractionated by gel electrophoresis and then transferred by capillary action to a suitable membrane. After blocking of nonspeci fi c binding sites, the nitrocellulose replica of the original gel electrophoresis experiment is then allowed to hybridize with an oligonucleotide probe representing the speci fi c DNA sequence of interest. Should speci fi c DNA be present on the blot, it will combine with the labeled probe and be detectable. By coelectrophoresing DNA fragments of known molecular weight, the size(s) of the hybridizing band(s) can then be determined. Southern blotting hybridization technology is one of the major tools that have already helped clinical staffs worldwide interpret genomic information. Other competing methodologies include in situ hybridization and solution hybridization. Important clinical examples of the use of this technology are DNA fi ngerprinting and the ability to detect DNA gene rearrangements.

In 1983, Dr. Kary Mullis at Cetus Corporation conceived of Polymerase Chain Reaction [ 9 ] . There is not a single technique that has had a greater impact on the practice of molecular biology than PCR. With this technique, we can detect infectious diseases agents at an extremely low level. It is based on the ability of sense and antisense DNA primers to hybridize to a DNA of interest. Following extension from the primers on the DNA template by DNA polymerase, the reaction is heat-denatured and allowed to anneal with the primers once again. Another round of extension leads to a multiplicative increase in DNA products. Therefore, a minute amount of DNA can be ef fi ciently ampli fi ed in an exponential fashion to result in larger amounts of DNA that are more easily manipulated. By including critical controls, the technique can be made quantitative. The current level of the sensitivity and detection limit is as low as 10-50 copies per ml blood in HIV testing [ 1, 10, 11 ] .

Important clinical examples of the use of PCR are detection of HIV and HCV [12] [13] [14] . PCR techniques have evolved into different branches. Some of them are now widely in use for virus detection in clinical diagnostics. These are real-time PCR by Taqman (Roche), Light Cycler (Roche) and Smart Cycler (Cepheid), and in situ PCR, nested-PCR, nested-real time PCR [ 15 ] , broad-range PCR, multiplex PCR, RT-PCR, arbitrarily primer PCR, long PCR, and quantitative PCR. Real-time sequence technology will be coming soon for more detailed detection. In the past, identi fi cation of viral serotypes was restricted to investigative methods using antibody detection and restriction fragment length polymorphism (RFLP). With real-time sequences technology, we will be able to detect a virus early as well as to obtain the viral sequence.

Microarrays were developed at Stanford University by Schena and coworkers in the early 1990s [ 16 ] . For medical applications, a microarray analysis offers a very accurate screening technology. It allows hundreds or thousands of nucleic acid hybridization reaction to be performed on a solid substrate. It promises to be a fast and accurate diagnostic tool in the fi eld of clinical microbiology and virology. Applied to infection safety for blood and blood products, it will be able to screen for the presence of viral pathogens by matching genetic sequences. Compared with existing technologies, it allows for a wider variety of speci fi c tests to be carried out simultaneously to determine the quality of the blood and will provide consumers with extra safety. With the use of molecular biology protocols, the microarray will permit the detection of lower concentrations of microorganisms in the blood and the accurate identi fi cation of many types of pathogenic contaminants. In the near future, progress can be expected in the application of microarray technology for screening of donated blood for infectious agents. It can provide vast information about the identity of bloodborne pathogens as well as their gene expression pro fi les [ 17 ] .

To ensure a safe blood supply for those who may need a transfusion, an important step in ensuring safety is the screening of donated blood for infectious agents. After donation, each unit of donated blood undergoes a series of tests for bloodborne agents such as human immunode fi ciency virus (HIV)-1, HIV-2, hepatitis B virus (HBV), hepatitis C virus (HCV), human T-Cell lymphotropic virus (HTLV)-1 and HTLV-II, West Nile virus (WNV), and Treponema pallidum , the agent of syphilis.

All of the above tests are referred to as screening tests, and are designed to detect as many infectious agents as possible. Because these tests are so sensitive, some donors may have a false-positive result, even when the donor has never been exposed to the particular infection. In order to sort out true infections from such false-positive test results, screening tests that are reactive may be followed up with more speci fi c tests called con fi rmatory tests. Thus, con fi rmatory tests help determine whether a donor is truly infected. If any one of these tests fails, affected blood products are considered unsuitable for transfusion [ 18 ] .

Nucleic acid testing (NAT) employs testing technology that directly detects the genomes of viruses. Because NAT detects a virus's genetic material instead of waiting for the body's response, the formation of antibodies, as with many current tests, it offers the opportunity to reduce the window period during which an infecting agent is undetectable by traditional tests [ 19 ] , thus further improving blood safety. NAT will become the gold standard because of greater sensitivity compared to antibody tests. Since 1999, NAT has been approved by the FDA and used to detect HIV-1 and HCV; this technology currently is under investigation for detecting other infectious disease agents. We know that for many viral infections, viral RNA appears very early in the infection, in 1-2 weeks, but the antibody does not appear until 10-12 weeks, e.g., HIV and HCV [ 20 ] . In order to virtually prevent infection by all the transfusion associated viruses, we need to detect the viruses in their window period, and a NAT or gene-based testing method is needed. NAT also provides an opportunity for the viral, e.g., HIV or HCV, infected donor to seek early treatment. On the other hand, NAT is not only a sensitive method, but also a rapid method which is suitable for a blood bank laboratory because the turnaround time for maintaining blood donations is extremely critical.

The HBV is a highly infectious and often nonsymptomatic virus that is transmitted primarily through blood and blood-derived fl uids and is a leading cause of liver infection worldwide. The World Health Organization (WHO) estimates that two billion people worldwide have been infected with HBV and 350,000,000 people are chronically infected. Chronic infection results in a high risk for liver cancer and cirrhosis of the liver, which cause about 1,000,000 deaths each year. Each year up to 200,000 people become newly infected in the United States alone. Since the beginning of screening for HBV in 1969, the rate of infection through blood transfusions has greatly decreased. However, as of 2000, HBV is still transmitted through blood transfusions in 1 out of 137,000 units of blood. One reason for this is that currently available blood screening technologies detect core antibodies or surface antigens, which appear up to 8 weeks after infection. Serologic tests for HBV include hepatitis B surface antigen (HBsAg) and hepatitis B core antibody (HBcAb).

HBV, which mainly infects the liver, has an inner core and an outer envelope (the surface). The HBsAg test detects the outer envelope, identifying an individual infected with the HBV. This virus can cause in fl ammation of the liver, and in the earliest stage of the disease, infected people may feel ill or even have yellow discoloration of the skin or eyes, a condition known as jaundice. Fortunately, most patients recover completely and test negative for HBsAg within a few months after the illness. A small percentage of people become chronic carriers of the virus, and in these cases, the test may remain positive for years. Chronically infected people can develop severe liver disease as time passes, and need to be followed carefully by an experienced physician. To reduce the occurrence of posttransfusion hepatitis, it is essential to screen all blood donations for HBsAg by the most sensitive and speci fi c assays. Blood donations that are found to be reactive in the HBsAg test are automatically con fi rmed by the HBsAg con fi rmatory assay. If the specimen is neutralizable in the con fi rmatory test, the specimen is considered positive for HBsAg. HBsAg testing of donated blood has begun in 1975 (Table 28.1 ) .

Currently, all blood donors are screened for HBsAg, but occasional transmission of HBV still occurs due to the inclusion of window period donations (i.e., blood from recently infected donors who are antibody negative but still viremic). Detection of early HBV infection of blood donors is still a major problem of blood transfusion. The current third-generation licensed HBsAg tests (mostly radioimmunoassay and enzyme immunoassays) can not detect HBV in the window period for HBV infection. This is a strong motivation for introducing molecular detection techniques to the fi eld. There are some commercially available test methods for detecting HBV DNA in the market now, such as Chiron's Quantiplex HBV DNA [ 21 ] , Digene's Hybrid Capture, Abbott's HBV DNA assay, and Roche's Amplicor HBV Monitor. Using these commercial hybridization or PCR-based assays, HBV DNA can be detected 1-3 weeks before the appearance of HBsAg [ 22 ] . Some chronically infected patients who have lost their HBsAg remain HBV DNA positive, but are disquali fi ed as potential blood donors. Molecular detection of HBV DNA is more sensitive than current methods employed for HBsAg screening.

Determination of antibodies to the hepatitis B core antigen (anti-HBc) (total) is also used to monitor the progress of the hepatitis B viral infection. Determination of anti-HBc (IgM) is employed to distinguish an acute hepatitis B infection from a chronic infection. The anti-HBc test developed in 1987 detects an antibody to the HBV that is produced during and after infection. If an individual has a positive anti-HBc test, but the HBsAg test is negative, it may mean that the person once had hepatitis B, but has recovered from the infection. Of the individuals with a positive test for anti-HBc, many have not been exposed to the HBV; thus, there is a frequent problem of false positives. Although the individual may be permanently deferred from donating blood, it is unlikely that the person's health will be negatively affected. (Note: This antibody is not produced following vaccination against hepatitis B).

The HCV is a member of the Flaviviridae family of viruses, which are associated with both human and animal diseases. Hepatitis caused by HCV is the most common chronic bloodborne infection in the United States. Over four million Americans are believed to be infected. HCV can also be transmitted through blood transfusion. HCV causes in fl ammation of the liver, and up to 80% of those exposed to the virus develop a chronic infection, which can lead to liver in fl ammation, cirrhosis, cancer, and death. Eventually, up to 20% of people with HCV may develop cirrhosis of the liver or other severe liver diseases. As in other forms of hepatitis, individuals may be infected with the virus, but may not realize they are carriers since they do not have any symptoms. Because of the risk of serious illness, people with HCV need to be followed closely by a physician with experience evaluating this infection. Since the fi rst cloning of fulllength HCV cDNA in 1989, signi fi cant progress has been made in characterizing its molecular biology [ 11 ] . But, the natural history of HCV infection is still largely unclear and current treatment options for patients are limited. There is no vaccine for HCV, and the only available treatment, a combination of alpha interferon and ribavirin, is ef fi cacious in only a minority of patients [ 23 ] . The life cycle of the HCV is poorly understood due to the lack of an ef fi cient cell culture system [ 24 ] . There is an urgent need to develop a highly sensitive detection method for studying possible extrahepatic sites for the replication of HCV. We have recently established a cell culture system for the replication of HCV by using human T and B leukemia cell lines [ 25 ] . This model should represent a valuable tool for the detailed study of the initial steps of the HCV replication cycle and for the evaluation of antiviral molecules. Currently, appropriate vaccine strategies for HCV have not been developed. Early detection and prevention of HCV infection are most important for blood safety.

It is a formidable task to design primers and probes for sensitive nucleic acid level diagnostic assays throughout the open reading frame of the HCV genome because of a high mutation rate in this genomic region. However, the untranslated region of about 341 nucleotides contains highly conserved domains which allows for stable primer design for qualitative and quantitative diagnostic tests which have equivalent sensitivity against the known six various genotypes of HCV.

In 1990, the fi rst speci fi c test for HCV, the major cause of "non-A, non-B" hepatitis was introduced. Now, a third generation ELISA kit is available to detect antibodies to HCV and screening blood for HCV antibodies is recommended. These assays are based on detection of serum antibody to various HCV antigens because these antibodies are nearly universally present in patients who are chronically infected with HCV [ 26 ] . The HCV screening tests are known to have signi fi cant limitations and positive samples should be further tested by HCV con fi rmatory tests.

Guidelines provided by the CDC recommend that HCV antibody screening test positive samples should be con fi rmed with serologic or nucleic acid supplemental testing. HCV con fi rmatory tests include the recombinant immunoblot assay in which several recombinant peptide antigens are applied on a strip that is then probed with the patient's serum. In this way, the response to individual antigens can be recognized, and some false-positive ELISA results can be eliminated (e.g., RIBA, Chiron HCV 3.0, and PCR assay) (e.g., Roche COBAS AMPLICOR HCV Test, version 2.0). Laboratories can choose to perform this testing on all positive specimens or based on screening test positive (signal to cutoff) ratios. The positive predictive values (s/co) can vary depending on the prevalence of infection in the population being screened.

HCV antibodies are not generally detectable for at least 6 weeks and may not appear for several months. Acute HCV infections are relatively rare among blood donors, but the antibody tests often fail to detect these patients in the window period between the time of infection and the time of appearance of antibody detectable by the above assays. High sensitivity detection of HCV during the window period is a longterm technical challenge in the fi eld. Tests for HCV RNA genome detection based on the PCR or other highly sensitive RNA detection systems have been used for the diagnosis of acute hepatitis [ 26 ] . Sensitive detection of HCV RNA based on RT-PCR or other nucleic acid ampli fi cation techniques can be readily accomplished with kits that are now available commercially. For example, in 1999 the FDA approved Roche's Amplicor HIV-1 Monitor Ultra Sensitive quantitative assay. It can measure HIV levels at as few as 50 copies/mL and another commercial kit, the LCx HIV RNA Quantitative Assay from Abbott Laboratories, also has a detection limit at 50 copies/mL. Some studies even showed a sensitivity limit at 1 copy [ 27 ] . In fact, a qualitative assay should be much more sensitive than a quantitative assay for HIV/HCV screening. A sensitive qualitative HCV molecular detection assay will possibly interdict and virtually prevent all transfusion-associated HIV/HCV. The current sensitivity standard for clinical diagnostics is 100 copies/mL, but since there has been an improvement in technology, this would be the time to change sensitivity standard to 50 copies/mL.

HIV-1 and/or HIV-2 virus cause acquired immunode fi ciency syndrome, or AIDS. The test is designed to detect antibodies directed against antigens of the HIV-1 or HIV-2 viruses. HIV-1 is much more common in the United States, whereas HIV-2 is prevalent in Western Africa. Donors are tested for both viruses because both are transmitted by infected blood, and a few cases of HIV-2 have been identi fi ed in US residents. In1985, the fi rst blood-screening EIA test to detect HIV was licensed and quickly implemented by blood banks to protect the blood supply. In 1992, testing of donor blood for both HIV-1 and HIV-2 antibodies (anti-HIV-1 and anti-HIV-2) was implemented. In 1996, HIV p24 antigen testing of donated blood was mandated. Now, the p24 antigen testing is going to be compared with a PCR-based test for their ability to detect HIV in the window period.

HTLV retroviruses are endemic in Japan and the Caribbean but relatively uncommon in the United States. They cause adult T-cell leukemia/lymphoma and a neurological disorder similar to multiple sclerosis. The infection can persist for a lifetime but rarely causes major illnesses in most people who are infected. In rare instances, the virus may, after many years of infection, cause nervous system disease or an unusual type of leukemia. HTLV-II infections are usually associated with intravenous drug usage, especially among people who share needles or syringes. Disease associations with HTLV-II have been hard to con fi rm, but the virus may cause subtle abnormalities of immunity that lead to frequent infections, or rare cases of neurological disease.

In 1989, human-T-lymphotropic-virus-antibody testing of donated blood was begun. Blood is now routinely screened for antibodies to HTLV-I/II. These test screens for antibodies directed against epitopes of the HTLV-I/II viruses. Several commercial assays based on the enzyme-linked immunosorbent assay (ELISA) or particle agglutination formats are used for screening of HTLV antibodies, followed by con fi rmatory assays using western blotting. In some infected individuals, the serologic response to HTLV infection is very low. These problems have been solved by the application of PCR ampli fi cation of speci fi c sequences in the virus genome. PCR can be used to detect HTLV-I/II proviruses and is now the method of choice for detection of HTLV DNA directly from blood and many other tissues. Commercial PCR kits for HTLV are available [ 28 ] .

The WNV is a single-stranded RNA virus of the Flaviviridae family and is the most recent emerging infectious disease threat to public health and, potentially, to the safety of our blood supply. In 2002, WNV was identi fi ed as transfusion transmissible. It is transmitted by mosquitoes to birds and other animals through a mosquito bite. The virus can infect people, horses, many types of birds, and some other animals. WNV was shown in 2002 to be transmissible by blood [ 29 ] , with an estimated mean risk of 2/10,000-5/10,000 in outbreak regions in the United States. The most common symptoms of transfusion-transmitted cases of WNV were fever and headache.

Detection of WNV includes either a measurement of WNV antibodies or of WNV nucleic acid (detecting genetic material from the virus itself). There are two types of WNV antibody testing: IgM and IgG. In most individuals, IgM antibodies will be present within 8 days after the initial exposure to WNV, followed by IgG production several weeks later. But, the antibodies tested to detect WNV are not expedient for donor blood screening. NAT involves amplifying and measuring the WNV's genetic material to detect the presence of the virus in blood or tissue. WNV NAT will be negative in the blood once clinical illness has occurred. In this situation, both NAT and IgM antibody testing may be needed. Nucleic acid tests to screen blood for WNV are commercially available and in current use. But, the viral yield for WNV infection is much lower than other viruses. Consequently, a more sensitive WNV NAT system for donor blood screening will be required, which could further reduce the risks of transfusion transmitted WNV.

Serum samples from all blood units should be subjected to either the Venereal Disease Research Laboratory (VDRL) test or a treponemal test, such as the T. pallidum haemagglutination (TPHA) test before transfusion. Any unit found positive should be discarded as per standard safety procedures. This test is done to detect evidence of infection with the spirochete that causes syphilis. Blood centers began testing for this shortly after World War II, when syphilis rates in the general population were much higher. The risk of transmitting syphilis through a blood transfusion is exceedingly small (no cases have been recognized in this country for many years) because the infection is very rare in blood donors, and because the spirochete is fragile and unlikely to survive blood storage conditions. Sensitivity and speci fi city of serologic tests vary depending on the type of test performed and the stage of the disease. If the donor has spirochetemia, their serologic tests are usually negative, and if the donors are antibody positive, their blood is not infectious. Syphilis serological tests for donors have less clinical signi fi cance. A nucleic acid test for accurately detecting syphilis is needed. It can be used to determine whether a blood donor is currently or has recently been infected with the spirochete.

In recent years, numerous infectious agents found worldwide have been identi fi ed as potential threats to the blood supply and among these are several newly discovered hepatitis viruses that present unique challenges in assessing possible risks. Even if the hepatitis virus test is negative for all known A-E hepatitis agents, there are some unidenti fi ed hepatitis viruses, called non A-E hepatitis viruses that can still be transmitted by blood transfusion. In the future, advances in NAT may allow rapid discovery of the unknown hepatitis viruses.

Hepatitis delta virus (HDV) is a small RNA virus that can infect only individuals who have HBV; worldwide more than 15 million people are coinfected [ 30 ] . HDV is clinically important because it generally makes HBV infections more damaging to the liver. Increased understanding of the molecular virology of HDV will identify novel therapeutic targets for this most severe form of chronic viral hepatitis. PCR and real-time PCR methods are available for HDV RNA detection [ 31 ] .

TT virus (TTV) [ 32 ] , named for the patient from whom it was fi rst isolated with non-A-E and G posttransfusion hepatitis in Japan in 1997, is a newly discovered transfusion transmitted, single-stranded and circular DNA virus [ 33 ] . TTV is nonenveloped and its entire sequence of ~3.9 kb has been determined. It is also often interpreted as a transfusion-transmitted virus [ 32 ] . At least 16 genotypes have been identi fi ed, and TTV is now found all over the world. TTV infection was sought by detection of TTV DNA in serum by polymerase chain reaction using primers generated from a conserved region of the TTV genome, e.g., the UTR region [ 34 ] . Donor blood and blood product can be screened for TTV DNA by using PCR or real-time PCR. The signi fi cance of positive fi ndings is still unclear, because high level TTV carriers in healthy populations are currently found [ 35, 36 ] . Whether TTV actually causes hepatitis remains to be determined.

Cytomegalovirus (CMV) is a virus belonging to the herpes group that is rarely transmitted by blood transfusion. Donor blood is not routinely tested for CMV, and the prevalence of CMV antibody ranges from 50 to 80 % of the population. But, blood contaminated with CMV can cause problems in neonates or immunocompromised patients. It also remains a major pathogen for solid-organ transplant recipients causing febrile syndromes, hepatitis, pneumonitis, retinitis and colitis. Potential problems in selected patient populations can be prevented by transfusing CMV negative blood or frozen, deglycerolized red blood cells. Serologic tests for antibody to CMV are useful for determining whether a patient had CMV infection in the past, a determination of great clinical importance for organ and blood donors, and in the pretransplant evaluation of prospective transplant recipients [ 37 ] . Commercial NAT kits are available for CMV [ 3 ] , and these include the Amplicor PCR CMV Monitor test and Hybrid capture system CMV DNA test.

Sensitive screening tests for malaria are neither commercially available nor of fi cially approved yet. The most effective way of screening donors is to take a proper history of malaria or of fever that could be due to malaria. Donor selection criteria should be designed to exclude potentially infectious individuals from donating red blood cells for transfusion. Because there are no practical laboratory tests available to test donor blood, donors traveling to high risk malaria areas are excluded from donating blood for 6 months. However, there is a need to develop suitable screening tests, especially for use in an endemic area. A number of clinical research approaches have been developed for the extraction, ampli fi cation and detection of malaria parasite DNA from blood products [ 37 ] .

Variant Creutzfeldt-Jakob disease (vCJD-a rare but fatal brain infection) [ 38 ] was fi rst described in 1996 in the United Kingdom. vCJD is strongly linked with exposure to the bovine spongiform encephalopathy (BSE) agent. BSE is a transmissible spongiform encephalopathy (TSE) affecting cattle and was fi rst reported in the UK in 1986. It has different clinical and pathologic characteristics from classic vCJD. Each disease also has a particular genetic pro fi le of the prion protein gene. In recent years, questions have been raised concerning the potential risk of vCJD disease for recipients of plasma-derived clotting factors, including United States licensed Factor Eight (pdFVIII), Factor Nine (pdFIX), and other plasma-derived products such as immune globulins and albumin. In the past 10 years, there have been some reported cases of probable vCJD transmission by red blood cell transfusions in the United Kingdom. Prion infections are associated with long and clinically silent incubations. The number of asymptomatic individuals with vCJD prion infection is unknown, posing risk to others through blood transfusion, blood products, organ or tissue grafts, and contaminated medical instruments. In order to decrease the risk, there is a need to establish a blood-based molecular assay for detection of vCJD prion infection. Recently research papers have shown that sensitivity detection methods are available for vCJD prion [ 39 ] . However, commercial detection kits are not yet available.

The Dengue virus (DENV) is a member of the virus family Flaviviridae and is transmitted to people through the bite of an infected mosquito. The Dengue virus has been shown to have four subtypes. These subtypes are different strains of dengue virus that have 60-80 % homology between each other. Dengue has emerged as a worldwide problem only since the 1950s. With more than one-third of the world's population living in areas at risk for transmission, dengue infection is a leading cause of illness and death in the tropics and subtropics. According to CDC, as many as 100 million people are infected yearly. Dengue is caused by any one of four related viruses transmitted by mosquitoes. There are not yet any vaccines to prevent DENV infection, and the most effective protective measure is to avoid mosquito bites. There have been healthcare-related transmissions, including transmission by blood products [ 40 ] . Dengue infection has a viremic phase that lasts 4-8 days, and blood collected during this phase may be infective when transfused into susceptible hosts [ 40 ] . There are currently no tests for direct detection of dengue virus, but there are however, commercial ELISA tests to detect antibodies of the dengue virus in blood samples from patients. Recently, research papers have shown that PCR detection methods are available for any dengue virus strain [ 41 ] .

Babesia is a protozoan parasite of the blood that causes a hemolytic disease known as Babesiosis. Babesiosis is a malaria-like parasitic disease, and there are over 100 species of Babesia identi fi ed. In the United States, Babesia microti is the agent most commonly reported to cause human infection. Clinical confusion between human babesiosis and malaria is often reported in literature [ 42 ] . Babesia infection can also be acquired by blood transfusion. In fact, there have been many cases of transfusioninduced babesiosis documented [ 43 ] . Risk of developing this clinical infection is increased for elderly, asplenic, or immunosuppressed patients. Current standards issued by the American Association of Blood Banks (AABB) require the inde fi nite deferral of a blood donor with a history of babesiosis. [ 44 ] There is a need to develop methods for identi fi cation B. microti in order to reduce the risk of transmission of babesiosis by transfusion. Diagnosis depends upon fi nding parasites on blood fi lm examination which can be detected 2-4 weeks after a tick bite. Hamster inoculation and serology have also been used for diagnosis. The Indirect Fluorescent Antibody Test (IFAT) is available for B. microti and is the most useful serological test for early diagnosis. Also, the PCR screen tests for Babesiosis are technically available in the fi eld [ 45 ] .

Chagas disease is named after the Brazilian physician Carlos Chagas, who discovered the disease in 1909. Chagas disease is spread mainly by blood-sucking insects infected with Trypanosoma cruzi . Chagas disease can also be spread through blood transfusion, organ transplants, and from a mother to an unborn child. National screening of the blood supply was instituted in early 2007 by FDA, and more than 1,000 donors with T. cruzi infection have been identi fi ed within the past 3 years of testing. "Screening for T. cruzi is an important safety measure to help protect our blood supply and to help prevent the spread of Chagas disease," says Karen Midthun, M.D., acting director of the FDA's Center for Biologics Evaluation and Research.

Currently, serological ELISA tests are available for diagnose chronic Chagas disease. PCR test is not a tool for diagnosis of chronic Chagas disease in clinical practice yet, although some research results have showed that PCR is a very sensitive parasitological test for Chagas' disease in active transmission regions [ 46 ] . More studies are needed for the development of this molecular method.

Coronavirus is an RNA virus known to be associated with respiratory disease. Severe acute respiratory syndrome (SARS) is a newly recognized coronavirus whose genome sequence does not belong to any of the known coronavirus groups and which quickly spread all over the world from Asia in 2003. There has been no evidence that this infection is transmitted from blood donors to transfusion recipients, but the virus associated with SARS is present in the blood of people who are sick, and it is possible that the virus could be present in blood immediately before a person gets sick, so that an individual with infection but no symptoms possibly could transmit SARS through a blood donation. To help determine whether or not an individual might be infected with SARS, a blood collection facility will ask a potential donor orally or in writing about any travel to a SARS-affected country or a history of SARS or possible exposure to SARS. Enzyme-linked immunoassays for detection of speci fi c IgG and IgM antibodies and RT-PCR for detection of SARS coronavirus speci fi c RNA in the SARS patients has been developed. Rapid, sensitive, and speci fi c identi fi cation of SARS and other novel coronaviruses by molecular methods will be very important in the future.

Based on past history, it is not just a hypothetical risk that many people have been infected with unrecognized viruses, for example, many patients with symptoms of non A-E, G, and TTV posttransfusion hepatitis. It is still possible that unexplained cases of posttransfusion hepatitis may be caused by a new, undiscovered pathogen. In recent years, numerous new infectious agents found worldwide have been identi fi ed through time-consuming procedures. By the time a new virus, such as HCV, HIV and SARS, is found, many people are infected and there could be a large number of fatalities. There is an urgent need to develop methods for rapid identi fi cation and characterization of previously unknown pathogenic viruses. The most recent technologies for detecting and identifying previously unrecognized pathogens are expression library screening, representational difference analysis (RDA), and broad-range polymerase chain reaction (BR-PCR). But they are all time-consuming approaches. The new unrecognized and uncharacterized viral agents can be rapid identi fi ed by some of the new molecular approaches, e.g., subtraction hybridization [ 47 ] and DNA microarray.

Ensuring the safety and ef fi cacy of blood and blood products is a critical regulatory challenge. The high safety level of the blood supply is the result of continued improvements in blood donor screening and testing. It will be achieved by introducing more updated nucleic acid tests to the fi eld of blood safety. NAT is a method of testing blood that is more sensitive and speci fi c than conventional tests that require the presence of antibodies to trigger a positive test result. Also, NAT works by detecting the low levels of viral genetic material present when an infection occurs but before the body develops an immune response to a virus. This improved sensitivity should enable us to signi fi cantly decrease the infection window period, allowing for earlier detection of the infection and diminishing the chances for transmission of the agent via transfusion. We are to protect the blood supply from not only known pathogens but also the emergence of new and unrecognized and uncharacterized infectious agents. The NAT methods are more sensitive and speci fi c compared with non-NAT. In the future, NAT technology, such as PCR, may allow routine screening of donors for all the known and unknown pathogens of concern to blood safety.

Progress in blood supply safety

Emerging infectious disease issues in blood safety

White TJ (eds) Molecular microbiology: diagnostic principles and practice

Evaluation of a new NASBA assay for the qualitative detection of hepatitis C virus based on the NucliSens Basic Kit reagents

Detection of piscine nodaviruses by real-time nucleic acid sequence based ampli fi cation (NASBA)

Molecular-based methods for quantifying HIV viral load

Molecular diagnostics of infectious diseases

DNA, 50 years of the double helix: from the concept of molecular hybridization to microarrays

In vitro nucleic acid ampli fi cation techniques

Multicenter evaluation of the performance characteristics of the nucliSens HIV-1 QT assay used for quantitation of human immunode fi ciency virus type 1 RNA

Serological and molecular biology screening techniques for HCV infection

Clinical evaluation of an HIV-1 and HCV assay and demonstration of signi fi cant reduction of the HCV detection window before seroconversion

HIV-1 Monitor UltraSensitive quantitative assay. Roche, Nutley 14. LCx HIV RNA quantitative assay from

Nested real-time PCR for hepatitis A detection

Introduction to microarray analysis

Development and validation of a diagnostic DNA microarray to detect quinolone-resistant Escherichia coli among clinical isolates

Testing requirements for communicable disease agents

Detection of HIV-1 and HCV infections among antibody-negative blood donors by nucleic acid-ampli fi cation testing

Immunization of health-care workers: recommendations of the advisory committee on immunization practices (ACIP) and the hospital infection control practices advisory committee (HICPAC)

Assessment of hepatitis B virus DNA stability in serum by the Chiron quantiplex branched-DNA assay

Section two: speci fi c virus families

Recent advances in prevention and treatment of hepatitis C virus infections

The scienti fi c challenge of hepatitis C

Hirsh fi eld I (2003) Detection of extrahepatic HCV replication by a novel highly sensitive single tube nested-PCR

Section two: speci fi c virus families

New real-time reverse transcriptase-initiated PCR assay with single-copy sensitivity for human immunode fi ciency virus type 1 RNA in plasma

Human T-cell leukemia virus types 1 and 2 (Chap. 58)

Estimated risk of transmission of the West Nile Virus through blood transfusion in the US

Hepatitis delta virus

Quanti fi cation of hepatitis delta virus RNA in serum by consensus real-time PCR indicates different patterns of virological response to interferon therapy in chronically infected patients

TTV-a virus searching for a disease

A novel unenveloped DNA virus (TT virus) associated with acute and chronic non-A to G hepatitis

Role of transfusion-transmitted virus in acute viral hepatitis and fulminant hepatic failure of unknown etiology

A novel DNA virus (TTV) associated with elevated transaminase levels in posttransfusion hepatitis of unknown etiology

TT virus

Section two: speci fi c virus families

Emerging infectious disease agents and their potential threat to transfusion safety

Detection of prion infection in variant Creutzfeldt-Jakob disease: a blood-based assay

Threat of dengue to blood safety in dengue-endemic countries

PCR detection of nearly any dengue virus strain using a highly sensitive primer cocktail

Do babesiosis and malaria share a common disease process?

Babesia infection through blood transfusions: reports received by the US Food and Drug Administration

Transfusion-transmitted Babesia spp.: bull's-eye on Babesia microti

Detection of Babesia species from infected dog blood by polymerase chain reaction

PCR-based diagnosis for Chagas' disease in Bolivian children living in an active transmission area: comparison with conventional serological and parasitological diagnosis

Rapid approach to identify an unrecognized viral agent

Complete list of donor screening assays for infectious agents and HIV diagnostic assays