Throughout history, at least three large “plague” pandemics were recorded: the First Pandemic, also known as the Plague of Justinian in the mid-6th century; the Second Plague pandemic, including the Black Death and the Great Plague of London over the 14th and 18th centuries; and the Third Pandemic, over the 19th and 20th centuries. Artistic and written documentation suggested a common etiological agent based on the descriptions of symptoms; however, direct evidence was only available for the most recent plague pandemic, where Yersinia pestis was identified as the causative agent of the disease by Alexandre Yersin (Zietz and Dunkelberg, 2004). The first retrospective diagnosis of skeletal remains from the Black Death (BD) used PCR and primers specific for Y. pestis to amplify and sequence individual aDNA fragments from the teeth of people suspected to have died of plague (Drancourt et al., 1998; Drancourt and Raoult, 2005). Although this study seemed to confirm Y. pestis as the pathological agent of the BD, some studies challenged the results, as Y. pestis could not be amplified from plague victims following stringent aDNA protocols (Gilbert et al., 2004). To settle the debate, new attempts were made to obtain Y. pestis from plague specimens using NGS approaches (Bos et al., 2011; Schuenemann et al., 2011). These results were performed in two separate labs and followed strict validation guidelines to demonstrate aDNA authenticity. Using hybridization capture and enrichment for sequences similar to modern Y. pestis strains, both teams were able to retrieve and reconstruct the ancient genomic sequence of Y. pestis from plague victims, finally proving that this pathogen was one of the infectious agents of the BD.

Similarly, the etiology of the Justinianic Plague was debated for several years until an aDNA study was able to identify Y. pestis as the causative agent (Harbeck et al., 2013). Later, a low-coverage whole-genome sequence of a Justinianic strain from Southern Germany (Wagner et al., 2014) allowed the first comparison of several ancient genome sequences involved in different pandemic events. A phylogenetic analysis from these strains showed that the lineage responsible for the Justinianic outbreak was distinct from the lineages in the Second and Third Pandemics and was placed between two extant Chinese strains recovered from rodents. These results were recently confirmed with a high-coverage whole-genome sequence from a different burial (Feldman et al., 2016). Mutations were identified that could have influenced the infectivity of the Justinianic strain; however, the high-coverage genome identified a number of false positive SNPs that were reported in the previous low-coverage genome, highlighting the advantages of higher coverage sequences and the use of quality criteria to confirm the authenticity of reported substitutions. Keller et al. (2019) took a conservative approach to assay mutations in low-coverage genomes recovered from a wide-range of first pandemic genomes across Europe, examining the micro-diversity present in strains at the time. The origins of other pandemics have also now been identified; for example, the origin of the Black Death during the Second European Pandemic was traced back to Eastern Europe, although the molecular mechanisms of virulence were observed to be similar between pandemics (Spyrou et al., 2019). Further, Rasmussen et al. (2015) applied a unique approach, utilizing a metagenomic sequencing analysis method of deeply sequenced human genomic data to obtain Y. pestis genomes from teeth of Late Neolithic/Bronze Age humans (5,000–3,500 yBP) and explore the earlier origins of this disease. This study showed that ancient Y. pestis strains were already infecting ancient human populations at least 3,000 years earlier than the first recorded pandemic; however, these ancestral strains lacked many of the key virulence genes required to infect humans today and that were present in the strains from the three plague pandemics (Rasmussen et al., 2015). Further research was able to describe the virulence factors present in ancient strains, as well as specifically the bubonic form of the pathogen, and further supported the origins of plague in Europe to the Bronze Age (∼3,000 yBP; Spyrou et al., 2018), providing key insights into the evolutionary processes behind the high pathogenicity of this organism.

The studies on Y. pestis clearly demonstrated the effectiveness of hybridization capture/enrichment techniques in ancient microbial DNA studies. For the first time, researchers were able to trace bacterial evolution temporally and geographically in ancient civilizations, and we now have detailed maps and information about how past pandemics originated and moved across Europe. These studies represented the first successful approaches to sequencing ancient microbial genomes and revealed the potential of ancient genomic studies for understanding how bacteria co-evolved alongside humans. Furthermore, the latest studies highlight the power of metagenomic sequencing approaches and mining deeply sequenced human specimens as a novel source of ancient microbial DNA. Future studies can also likely examine the presence of Y. pestis outside of Europe; for example, exploring these strains in non-human mammals or insect vectors would also be an avenue to pursue to investigate host-adaptation and how its interactions with humans have shaped its evolutionary history.

Mycobacterium tuberculosis is one of the most prevalent pathogens in human history (Müller et al., 2014) and remains the second largest cause of infectious disease deaths even today (Ottini and Falchetti, 2010; Dabernat et al., 2014). Along with other genetically similar Mycobacterium species, collectively known as the Mycobacterium tuberculosis complex (MTBC), it is the predominant etiological agent in the development of tuberculosis (TB). M. tuberculosis is the most widely studied pathogen in palaeomicrobiology (Zink et al., 2007), as it has been identified in hundreds of ancient individuals from various geographical regions and across several historical periods.

Mycobacterium tuberculosis was the first ancient bacterial pathogen to be studied using biomolecular methods. Initial palaeomicrobiological research on M. tuberculosis concentrated on the identification of the pathogen via PCR within ancient individuals who displayed osteological damage indicative of tuberculosis (Spigelman and Lemma, 1993; Tsangaras and Greenwood, 2012). Early PCR amplification studies focused on the identification of ribosomal proteins and insertion sequences specific to MTBC, and further characterization was performed using spoligotyping (spacer oligotyping (Taylor et al., 1999; Zink et al., 2002, 2007; Fletcher et al., 2003). However, these aDNA results were criticized for their unsuitability for phylogenetic analysis, poor reproducibility, and environmental contamination (Wilbur et al., 2009; Müller et al., 2014). More appropriate molecular approaches have since been applied, such as PCR methodologies to target single nucleotide polymorphisms (SNPs) and large sequence polymorphisms (LSPs) that provide power to infer phylogenetic relationships among ancient and modern samples (Bouwman et al., 2012; Müller et al., 2014).

PCR evidence of ancient M. tuberculosis was obtained from several prehistoric samples (before 3,000 BCE) (Salo et al., 1994; Nerlich et al., 1997; Crubézy et al., 1998; Hershkovitz et al., 2008), and suggested a long-term co-occurrence of the pathogen and humans. Most of these studies characterized a few loci within MTBC and provided evidence of the emergence of certain TB strains through time. However, they failed to provide information about particular genomic changes that differentiate specific strains or pathogenicity traits (Zink et al., 2007). Further, some loci utilized as markers of the MTBC, such as the insertional sequence IS6110, were widely used in ancient palaeomicrobiology studies (Tsangaras and Greenwood, 2012) and have since been shown to be conserved in both the human-infecting lineages of MTBC and soil isolates within the Mycobacterium family, making identification from buried ancient samples dubious (Wilbur et al., 2009; Müller et al., 2016). In light of this, hybridization enrichment techniques have been utilized to obtain whole genomic information to identify the origins of M. tuberculosis and to examine its recent history.

Ancient genomes from Mycobacterium species present a lower-than-average damage pattern among all the ancient bacterial genomes studied to date. This has been attributed to a robust cell wall and high G-C content which may help limit bacterial DNA degradation by protecting and stabilizing DNA molecules (Zink et al., 2002; Hershkovitz et al., 2008; Tsangaras and Greenwood, 2012). Recent studies have expanded the analysis of ancient M. tuberculosis to examine human migration and demographic changes by analyzing DNA sequences from a variety of geographical areas and across different times (Bouwman et al., 2012; Darling et al., 2014). While previous studies amplified a limited number of markers, new studies targeted multiple loci or whole genomes from multiple samples to obtain adequate resolution and disentangle complex relationships and migration histories. NGS analysis and enrichment capture methods improved phylogenetic resolution, allowing researchers to answer more complex questions, such as the origin of tuberculosis in ancient archaeological samples from the Americas (Bos et al., 2014). Whole genome sequences of modern and ancient M. tuberculosis genomes from South America and Europe revealed that South American human TB isolates were most closely related to TB strains from seals. This finding suggests that early South American TB strains may have resulted from a zoonotic transmission event, followed by a possible dispersal throughout humans in the Americas (Bos et al., 2014).

Research on ancient M. tuberculosis reflects the evolution of the field of palaeomicrobiology, from the single gene identification via PCR to whole genome reconstruction using NGS technologies. Ancient TB research has also provided insight into the dangers of assessing partial genomic sequences without proper environmental controls and highlights the need to consider mixtures of multiple related species within the same sample (e.g., environmental and human-associated Mycobacterium). Despite this, whole genome sequences have elucidated the evolutionary history, origins, and migrations of modern lineages. Further, whole genome sequences from ancient and modern M. tuberculosis strains, from different geographical sources and covering a large time-transect, will provide increased resolution of evolutionary events and adaptations that are elusive to our current models. Using ancient TB as a model system to examine specific evolutionary questions will undoubtedly improve our understanding of microbial evolution and distribution in human and animal populations throughout the world and across time.

Mycobacterium leprae is the infectious agent of leprosy, a chronic disease that has likely infected humans since prehistoric times (Donoghue, 2013; Mendum et al., 2014). Although nowadays it is most commonly found in undeveloped countries outside of Europe, archaeological and historical evidence, such as the establishment of several leper colonies, indicates leprosy was endemic in the medieval Europe, until it inexplicably vanished in the 16th century while increasing its prevalence in America and Africa (Schuenemann et al., 2013; Mendum et al., 2014; Andam et al., 2016; World Health Organization [WHO], 2016). M. leprae is an obligate intracellular pathogen with a slow growth rate (∼14 days generation time in humans), high genomic conservation between strains (i.e., <0.01% difference), a high number of pseudogenes (41% of its genome), and the loss of several housekeeping (conserved) genes (Cole et al., 2001; Monot et al., 2005; Schuenemann et al., 2013; Mendum et al., 2014). These features suggest that the M. leprae has undergone genome reduction or degradation similar to that reported during the evolution of other intracellular pathogens and symbionts (Cole et al., 2001; Ochman and Moran, 2001; Monot et al., 2005; Schuenemann et al., 2013). Initial palaeomicrobiological studies used PCR to characterize M. leprae from skeletal remains that exhibited osteological lesions indicative of leprosy (i.e., palate and nasal bone thinning) (e.g., Spigelman and Lemma, 1993); however, the majority of these studies did not comply with the criteria required for their authentication, rendering their results questionable.

Complete genomes of ancient M. leprae were recently recovered from medieval European samples (Schuenemann et al., 2013; Mendum et al., 2014). These studies obtained draft M. leprae genomes and found very few sites of differentiation in comparison to modern strains. In addition to following the basic guidelines for authentication of aDNA, ancient human mitochondrial DNA was also obtained by enrichment as an additional control for their authenticity. While the recovered mtDNA had distinctive damage patterns consistent with aDNA, the aDNA from M. leprae showed much lower levels of damage, raising further questions about decay kinetics of DNA in thick-outer-walled Mycobacterium species. Phylogenetic analyses of the ancient strains found them to cluster within a group containing modern Near East and Central Asia strains (Branch 2), as well as a group containing American strains and previously reported ancient European samples from a later period (Branch 3). This suggests that ancient strains from Branch 2 and 3 co-occurred in Europe, but eventually the Near Eastern and Asian strains were replaced by Branch 3, which later spread to the Americas (Schuenemann et al., 2013; Mendum et al., 2014). There also appeared to be little to no genetic evidence for virulence reduction in modern compared to ancient M. leprae. This is a critical finding and contradicts hypotheses that the declining incidence of leper cases in Europe through time was due to genomic changes in the pathogen. Instead, the reduction was likely caused by alternative factors, such as altered living conditions, changes in human immunity, novel protective factors, or alterations in co-infection dynamics (Schuenemann et al., 2013; Mendum et al., 2014).

Together, modern and ancient M. leprae DNA comparisons show a surprisingly low level of genomic variation since the divergence of the different lineages (∼3,000 years ago). Further work should explore and compare additional whole genomic sequences of various strains of all Mycobacterium species through time to explore the unique evolutionary history of this diverse genus (Harkins and Stone, 2015). Lastly, the low genetic variation and geographical associations revealed through the use of aDNA has highlighted the influence of human migrations in the propagation of this microbe in the past, suggesting trade paths such as the Silk Road as possible origins of transmission in the medieval era (Monot et al., 2009). This shows how palaeomicrobiology can do more than confirm past diagnoses, but rather contribute to the development of new hypotheses and other fields, such as history, epidemiology, and archaeology.

Cholera is an intestinal disease caused by infection with Vibrio cholerae. In the past 200 years, seven cholera pandemics (V. cholerae serotype O1) have been recorded worldwide, which were all attributed to two biotypes, distinguishable by several phenotypic markers: classical and El Tor (Harris et al., 2012). Cholera investigations based on disease etiology of early epidemics suggest that the O1 classical biotype may have been dominant before the last century. To test this hypothesis, Devault et al. (2014) reconstructed a near complete genome of an ancient V. cholerae sampled from a 19th-century preserved intestine of a patient deceased during the second cholera pandemic. This study identified the ancient strain as a “classical” biotype (serotype O1), confirming previous speculations that earlier pandemic events were caused by this strain (Devault et al., 2014). Whole genome sequence comparisons between modern and ancient strains also revealed high levels of genomic conservation, suggesting that the evolution of the modern pathogen has been under selective constraint during the past two centuries. However, it remains unclear how prevalent cholera was in more ancient periods.

Evidence suggests that the pathogenic strains involved in the last pandemics originated in Asia, so a more detailed exploration of ancient skeletons from that area could provide important insights into its origins. Sequencing aDNA from other sources, such as coprolites or mummified tissues, could also help identify V. cholerae in ancient specimens from populations with poor medical records, and also provide contextual information on how its infections may have impacted the gut microbiota of its inhabitants. Future studies on ancient V. cholerae could analyze dated human genomes or microbiomes that date to cholera pandemic events to investigate if ancient human populations were similarly affected by different strains of V. cholerae, and if genomic changes potentially supported the origination of this human pathogen. Moreover, additional dated ancient genomes could help to establish evolutionary rates of V. cholerae and add a temporal dimension to the studies.

Helicobacter pylori is one of the most prevalent human-associated microorganisms and can play commensal or pathogenic roles. It is present in more than 50% of the global population, and several strains can be associated with development of chronic gastritis and gastric ulcers (Disotell, 2003; Secka et al., 2014). Modern day populations of H. pylori cluster into seven geographically associated prototypes, and the most common prototype in Europe (hpEurope) is known to carry a recombinant genomic sequence from Asian and African prototypes (Secka et al., 2014). Due to its long association with humans (∼100,000 years), wide global dispersal, and high sequence diversity, this microorganism has been used to trace past human migrations (Falush et al., 2003). Genomic sequences from ancient H. pylori from the “Iceman” (a 5,300-year-old European glacial mummy) were retrieved using hybridization capture enrichment (Maixner et al., 2016). Surprisingly, the genomic sequences of the ancient H. pylori resembled the Asian prototype, suggesting a migration of the African strain into Europe some time after 5,300 BP. The researchers also assessed the potential impact that these bacteria had in the ancient human gut and identified 22 proteins associated with inflammatory response similar to those expressed in modern humans infected by H. pylori.

Due to the long association with humans and a low mortality rate from H. pylori infection, studies of this microorganism allow us not only to obtain insights into its evolution and pathogenicity, but also the health and migrations of ancient human populations. In studies involving H. pylori, the availability of well-preserved samples from ancient guts is scarce; however, similar studies could be conducted on other commensal species not present in the gut. For example, an analysis of commensal microbes present in dental calculus could provide an opportunity to identify new marker species to track human migrations (Eisenhofer et al., 2019), and examine how truly commensal isolates evolve alongside humans, in contrast to pathogens with different selective pressures.

Salmonella enterica is commonly referred to as a food-borne illness that causes gastroenteritis (non-typhoidal salmonellosis) with over 93.8 million cases globally each year (Majowicz et al., 2010). However, certain S. enterica serovars, such as S. Typhi and S. Paratyphi, are human-specific pathogens that can cause enteric fevers (Typhoid and Paratyphoid fevers, respectively) and can have lethal consequences, both in the past and today. While over 21 million cases of Typhoid still occur annually today around the world (Crump et al., 2004), their origins remained poorly understood until recently (Achtman, 2016). Two aDNA studies have examined the origins of Typhoid in both the Old and New Worlds. Zhou et al. (2018) were able to compare modern S. enterica ser. Paratyphi C strains to a single ancient strain recovered from bones and teeth in Norway that date to 1,200 CE. Using updated genomic evolutionary rates and comparative analysis to modern strains in pigs, boars, and chickens, Zhou et al. (2018) conclude that S. Paratyphi C likely originated during porcine domestication about ∼4,000 years ago in Europe. In the New World, S. Typhi was linked to a cocoliztli outbreak from a 16th century site in modern Mexico, several years after the first Europeans arrived in the region in 1511 (Vågene et al., 2018).

While these and other studies seem to suggest an Old World origin for S. Typhi (Achtman et al., 2012), deeper origins cannot be ruled out (Vågene et al., 2018). The recent study by Zhou et al. (2018) concludes that origin of S. Paratyphi dates back 3,428 years ago, although early genetic dating estimates still suggest that S. Typhi may have arisen 10,000–43,000 years ago (Roumagnac et al., 2006). Further, little is known about the distribution of S. Typhi in historic and ancient times outside of Europe and where it may have arisen, especially considering its links to animal domestication. Studies examining both domesticated and non-domesticated animal microbiota may reveal commensal Salmonella strains in the past, providing insight into the evolution of this diverse genus. Further still, its presence in the New World and the potential effects, both social and biological, on New World Indigenous peoples needs further exploration; for example, understanding how resistance or survival of S. Paratyphi influenced downstream immune responses or microbiota may be critical to better understanding Indigenous health in the Americas (Skelly et al., 2018).

Recently, paleomicrobiological tools have been applied to studies beyond bacteria to include viruses, parasites, and fungi, both from humans, animals, and the environment. Ancient viruses have emerged as accessible aDNA targets to better understand the origins of human disease in real-time. For example, the genome of the Variola virus, which causes small pox, was recovered both from 20th century strains and a child mummy from the middle of the 17th century (Duggan et al., 2016), suggesting that much of the variola viral evolution examined today has occurred in the past several hundred years (Duggan et al., 2016; Wertheim, 2017). Similar approaches were utilized to exclude a paleopathological diagnosed case of ancient smallpox (Ross et al., 2018). Additional ancient viral studies have explored the much deeper evolutionary history between viruses and humans, including hepatitis B (HBV) (Krause-Kyora et al., 2018; Mühlemann et al., 2018a; Ross et al., 2018) and parvovirus (Mühlemann et al., 2018b). Similar research projects are emerging in ancient parasites, namely in Plasmodium species to trace the origins of malaria. Marciniak et al. (2016) were able to verify the presence of P. falciparum DNA from a suspected Italian malarial outbreak in 1st–2nd century CE, while Gelabert et al. (2016) connected historic European Plasmodium strains to those circulating in the Americas, suggesting that Europeans may have introduced malaria into the Americas. These studies highlight the power of aDNA to track the origins and suspected histories of all pathogens, not only bacteria.

While many of these studies have reconstructed DNA from viral or eukaryotic pathogens in historic times, researchers can now examine the deeper evolutionary history and origins of these microbes. For example, tracking the long-term rates and directionality of viral evolution in Paleolithic humans and other hominids, such as Neanderthals, is now a possibility (Weyrich et al., 2017). Ancient DNA studies of viruses in other primates would also allow us to better calibrate and understand long-term viral evolution in hominids. Tracing back the environmental origins of ancient malarial strains, perhaps from preserved mosquitos or unique environmental samples, would also be important to better trace is distribution in the ancient past. Despite the exciting new questions that can be approaches using aDNA, it is also clear that strict aDNA methodologies must be performed during ancient viral and eukaryotic studies, as in bacterial studies, as the reliability of several ancient viral studies has already been questioned in the literature (Porter et al., 2017; Duchêne and Holmes, 2018).

The current study of ancient microbial pathogens has been mainly driven by the progress and accessibility of DNA sequencing technologies and sample availability. The early use of aDNA methodologies provided the opportunity to identify ancient pathogens for the first time and add a temporal dimension to the evolutionary history of important human microbial pathogens. Early palaeomicrobiological studies also used single or a restricted number of loci and provided only limited descriptions of temporal and geographic distributions of pathogens within human populations. In some cases, early studies even mistakenly identified environmental or non-pathogenic species that shared sequence with their pathogenic counterparts (Müller et al., 2016). Further, these early studies did not provide insight into genome-wide changes that allow organisms to increase or reduce their pathogenicity and adapt to niches, nor did they allow researchers to determine where specific strains originated.

The invention of NGS technologies has had a major impact on the field of palaeomicrobiology, allowing researchers to amplify, target, and retrieve specific aDNA sequences from a variety of microorganisms and reconstruct partial or whole genomes. By comparing near-complete genomes of ancient and modern microbial pathogens, researchers have been able to describe differences between strains, interrogate the evolution and acquisition of virulence mechanisms, and the social and biological mechanisms that underpin pathogen origins. By identifying the genomic changes in pathogenic microorganisms through time, and comparing their effects on ancient and modern populations, we are beginning to track the origins of modern disease, trace the underlying causes of pandemics, and monitor microbial evolution in real time.

Because of their relevance to human health and the availability of the samples, the majority of palaeomicrobiological studies have concentrated on the diagnosis and identification of ancient pathogenic organisms involved in historical pandemics that typically cause acute, highly lethal diseases. However, symbiotic, non-pathogenic microorganisms also have a significant impact on human health by playing commensal or mutualistic roles. Many commensal microorganisms are evidence of a long-standing, co-evolutionary relationships; however, commensal bacteria can become opportunistic pathogens depending on the environmental conditions, albeit those conditions are poorly understood. Therefore, it is important to examine not only pathogens, but also the symbiotic microorganisms in the body and the micro-ecological context in which pathogens are successful. Infectivity and disease success can be highly influenced by competition (for similar nutritional resources or space) and cooperation between microorganisms, and this complex network of interactions has not yet been fully examined in palaeomicrobiological studies. For example, the dental caries causing pathogen, Streptococcus mutans, has competition from multiple other Streptococcus species that are routinely known to inhabit the oral cavity, but it remains unclear with other Streptococcus species were more dominant before the rise of S. mutans associated with the adoption of agriculture (Cornejo et al., 2013). For this purpose, future research should explore the connection and relationship between individual bacterial genomes of commensal species and the related microbiota to ascertain how genomic differences correlate with selective pressures or alterations in the microbial community. Correlations between the prevalence of certain microbial communities and a pathogen could provide information on disease susceptibility and a powerful new way to assess past population morbidity and health, especially in non-infectious diseases. Further still, non-lethal pathogens can provide information about the evolution of commensalism and serve as proxies to understand human interactions and movements. Examples of these endemic oral microbes include Streptococcus, Neisseria, and Actinomyces species (Avila et al., 2009). Future microbial community analysis may also reveal other species that would be better targets to answer these questions.

Future palaeomicrobiology studies should include further research on non-bacterial microorganisms. Whole-genome sequences of ancient yeasts, viruses, fungi, and parasites are emerging, demonstrating how aDNA can provide, as in the case of bacterial pathogens, important insights into their evolution, both within humans and the environment. For example, the study of ancient yeast is an important issue, as they have played critical roles in disease development in humans, such as dental decay (Brighenti et al., 2014; Koo and Bowen, 2014), as well as in the fermentation and preservation of food products (Gibbons and Rinker, 2015). Future efforts could be applied to understand the impact of human selection and interaction on fermentation and preservation yeasts through time. An important advantage of yeasts is their ability to form spores, which are resistant to a variety of environmental stresses and may provide unique opportunities for preservation, although new extraction methodologies will likely need to be developed, as has been done for many other species (Shapiro et al., 2019). Furthermore, the interaction of human-associated yeasts and their products, such as fermentation, could have had an identifiable impact on human evolution and alterations of the human microbiome.

Two key human tissues have been utilized in many of the studies described in this review – bones and teeth. However, recent aDNA applications included microbiome containing specimens, such as dental calculus or coprolites, and have expanded our view of appropriate ancient specimens for palaeomicrobiological analysis (Tito et al., 2008; Adler et al., 2013). Further still, some recent samples have examined unique human-associated samples, such as calcified abscesses or kidney stones (Kay et al., 2014; Devault et al., 2017). Further still, well-preserved soft-tissue samples have also been shown to contain human microbiota, such as the “Iceman” mummy, although these are notably scarce. As our ability to accurately identify ancient microbes expands, novel sample types should be explored as sources of ancient bacteria, including pathogens, non-lethal pathogenic species, or commensal species. Unique sample types may include different human tissues, such as hair (Tobler et al., 2017), human associated archaeological materials, such as pots, ochre (Lenehan et al., 2017), or pitch (Jensen et al., 2019), or even human-associated microbes preserved in environmental specimens, such as ice (Turney et al., 2020), calcium carbonate (Frisia et al., 2017), or marine and terrestrial soils (Tobler et al., 2017). The use of new specimens will certainly further our understanding of the origins and evolution of many human-associated microbes, although attention to proper authentication criteria must be considered in all cases. Minimally, the integration of unique sample types will increase the available geographic and temporal range of ancient microbial genomes.

Most of the palaeomicrobiological studies to date have been conducted on human samples. However, domestic and wild animals are an important source of diseases, and many ancient pathogens may have been transferred between animals and humans, especially during the Neolithic Revolution when agricultural practices including animal husbandry were adapted (Wolfe et al., 2007). Where available, conserved remains from animals should be explored for pathogens. Plague is a good example of cases where animals played an important role in the transmission of disease to humans, although the roles that zoonotic vectors played in other ancient diseases remains unknown. Investigations into human pathogens with animal or insect reservoirs would also provide key information about pathogen-host co-evolution. As we expect rates of evolution to be variable across different microbes and/or strains in specific hosts, clear attention to the calculation of evolutionary rates and how these are influenced by mis-mapping or contamination will be key (Key et al., 2017; Bos et al., 2019). Studies exploring animal microbiomes could also provide information into the health and morbidity of ancient animals, help define their interactions with humans, and even provide details about their domestication, migration, and adaptation to past environments.